OA16478A - Fused dihydrofurans as GPR119 modulators for the treatment of diabetes, obesity and related disorders. - Google Patents

Abstract

The present invention relates to compounds of general formula (I), <img file="OA16478A_A0001.tif"/> wherein the groups R1 , LP , LQ, X1 , X2 , X3 , A, n and m are as defined in the application, which have valuable pharmacological properties, and in particular bind to the GPR119 receptor and modulate its activity.

Description

Boehringer Ingelheim International GmbH

New compounds, pharmaceutical compositions and uses thereof

Field of the invention

The présent invention relates to new compounds, in particular compounds of the formula I

R—N

wherein the groups R¹, L^p, L^Q, X¹, X², X³, A, n and m are defined as hereinafter, to processes for preparing such compounds, to pharmaceutical compositions, to their use as modulators of the G-protein-coupled receptor GPR119, to methods for their therapeutic use, in particular in diseases and conditions mediated by the modulation of the G-protein-coupled receptor GPR119, and to pharmaceutical compositions comprising them.

Background of the invention

Diabètes mellitus is a serious metabolic disease which affects more than 100 million people worldwide. In the USA there are more than 12 million diabetics with 600,000 new cases diagnosed every year. The prevalence of diabètes mellitus is increasing, which means in particular a high frequency of complications as well, leading to a substantial impairment of quality of life and life expectancy. Because of diabetes-associated microvascular complications, in the industrialised countries type 2 diabètes is currently the most common cause of adult-onset loss of vision, rénal insufficiency and amputations. In addition, type 2 diabètes is associated with a two- to five-fold increase in the risk of cardiovascular disease.

The UKPDS study (United Kingdom Prospective Diabètes Study) showed that intensive treatment with common therapeutic agents, e.g. metformin, sulphonylureas or insulin, results in only a limited improvement in glycaemic control (différence in the HbA1c value ~ 0.9%). Moreover, glycaemic control deteriorated considerably over time even in patients in the intensive treatment group, and this was put down to a détérioration in beta cell function. Diabètes is also a major cause of damage to the retina at the back of the eye and increases the risk of cataract and glaucoma. Finally, diabètes is associated with nerve damage, particularly in the legs and feet, which affects the patients ability to feel pain and contributes to serious infections. AU in ail, complications of diabètes are one of the major causes of death worldwide.

Adiposity (obesity) is the resuit of an imbalance between calorie intake and energy consomption, it correlates to a high degree with insulin résistance and diabètes. However, the molecular mechanisms that are involved in obesity/diabetes syndromes are not yet clear. At an early stage of the development of obesity, an increased insulin sécrétion balances out the insulin résistance and protects the patient from hyperglycaemia. However, after a time, the beta cell function worsens and non-insulin-dependent diabètes develops in about 20% of the obese population. Obesity has thus become a critical risk factor for diabètes, but the factors that prédisposé one group of patients to a pathological change in insulin sécrétion as a response to the accumulation of fat are currently unknown. Obesity also significantly increases the risk of the development of cardiovascular disease. Diabètes is also implicated in the formation of kidney complaints, eye complaints and problems of the nervous System. Kidney disease, also known as nephropathy, sets in when the filtering mechanism of the kidneys is disrupted and proteins escape into the urine in excessive amounts and finally the kidney fails. Therefore there is a medical need for médicaments for preventing and/or treating metabolic disorders (particularly diabètes, predominantly type 2 diabètes) and the complications thereof. In particular there is a need for médicaments with good activity in terms of glycaemic control, disease-modifying properties and reducing cardiovascular morbidity and mortality, and which also hâve a better safety profile.

Dyslipidemia is a disorder of lipoprotein metabolism, including lipoprotein overproduction or deficiency. Dyslipidemias may be manifested by élévation of the total cholestérol, LDL cholestérol and triglycéride and free fatty acid concentrations, and a decrease in high-density lipoprotein (HDL) cholestérol concentration in the blood. Dyslipidemia occurs often in situations including diabètes, a common cause of lipidemia. For adults with diabètes, it has been recommended that the levels of LDL, HDL, and total cholestérol, and triglycéride be measured every year. Optimal LDL cholestérol levels for adults with diabètes are less than 100 mg/dL (2.60 mmol/L), optimal HDL cholestérol levels are equal to or greater than 40 mg/dL (1.02 mmol/L), and désirable triglycéride levels are less than 150 mg/dL (1.7 mmol/L).

GPR119 is a G-protein coupled receptor (also known as GPCR2, RUP3, SNORF25 or GDIR) which is expressed predominantly in the beta celis of the pancréas and in the K- and L-cells of the intestine. The GPR119 receptor and isoforms hâve been identified in mammalian species including human, rat, mouse, hamster, chimpanzee, rhésus monkey, cattle and dog. The expression of GPR119 in the pancréas and particularly in the pancreatic β-cells led to the hypothesis that the GPR119 receptor could hâve effects upon insulin sécrétion. Activation of the receptor stimulâtes the cAMP signal pathway, increasing the intracellular levels of cAMP in these cells. This will lead to an improved diabetic situation by a dual action of such a compound: stimulation of cAMP in the beta cell occurs directly via activation of GPR119 in these cells and furthermore indirectly via stimulation of the release of neuroendocrine peptides like GIP and GLP-1 and PYY from the gut. The release of these peptides may hâve also additional bénéficiai effects, e.g. on food intake, gastric emptying and other yet unknown functions. Also, a GPR119 agonist can be expected to bring about an improvement in the beta cell function and the beta cell mass. In fact, activation of GPR119 stimulâtes insulin sécrétion in-vitro and in-vivo (in rodents) in a glucose-dependent manner. The discovery of two endogenous ligands, lysophosphatidylcholine (LPC) and oleoylethanolamide (OEA) as well as more potent GPR119 agonists hâve led to the characterization of GPR119 as both an insulin and incretin (GLP-1 and GIP) secretagogue receptor capable of lowering plasma glucose and thereby facilitating glycémie control without the risk of hypoglycemia (Biochem. Biophys. Res. Comm. 2005, 744-751; Cell Metabolism 2006, 167-175; Endocrinolgy 2007, 2601-9). It has recently been shown that GPR119 agonists effectively lower the blood glucose levels in diabetic rodents without the risk of hypoglycaemia. GPR119 knockout animais hâve shown that both insulin and incretin sécrétion induced by GPR119 agonists are dépendent upon GPR119 receptor. In addition, it has been shown that GPR119 agonists decrease food intake resulting in weight loss in Sprague Dawley rats. Therefore the GPR119 agonists may be expected to hâve a therapeutic benefit in metabolic diseases. Examples of such diseases include type 1 diabètes, type 2 diabètes, insufficient glucose tolérance, insulin résistance, hyperglycaemia, hyperlipidaemia, hypercholesterolaemia, dyslipidaemia, syndrome X, metabolic syndrome, obesity, high blood pressure, chronic systemic inflammation, retinopathy, neuropathy, nephropathy, atherosclerosis, endothélial dysfunction and bone-related diseases (such as osteoporosis, rheumatoid arthritis or osteoarthritis).

For comparison and additional information also see

1. Dhayal, S., Morgan, N. G. The significance of GPR119 agonists as a future treatment for type 2 diabètes. Drug News Perspect. 2010, 23(7), 418-24.

2. Yoshida, S.₍ Tanaka, H., Oshima, H., Yamazaki, T., Yonetoku, Y., Ohishi, T., Matsui, T., Shibasaki, M. AS1907417, a novel GPR119 agonist, as an insulinotropic and β-cell preservative agent for the treatment of type 2 diabètes. Biochem Biophys Res Commun. 2010, 400(4), 745-51.

3. Jones, R. M., Leonard, J. N., Buzard, D. J., Lehman, J. GPR119 agonists for the treatment of type 2 diabètes. Expert Opinion on Therapeutic Patents 2009, Vol. 19, No. 10: 1339-1359.

Aim ofthe présent invention

The aim of the présent invention is to provide new compounds, in particular new

2,3-dihydro-benzofuran-2-yl-piperidine dérivatives, which are active with regard to the G-protein-coupled receptor GPR119.

Another aim of the présent invention is to provide new compounds, in particular new 2₎3-dihydro-benzofuran-2-yl“piperidine dérivatives, which are agonists of the G-protein-coupled receptor GPR119. vy

A further aim of the présent invention is to provide new compounds, in particular new 2,3-dihydro-benzofuran-2-yl-piperidine dérivatives, which hâve an activating effect on the G-protein-coupled receptor GPR119 in vitro and/or in vivo and possess suitable pharmacological and pharmacokinetic properties to use them as médicaments.

A further aim ofthe présent invention is to provide effective GPR119 agonists, in particular for the treatment of metabolic disorders, for example diabètes, dyslipidemia and/or obesity.

A further aim of the présent invention is to provide methods for treating a disease or condition mediated by the activation the G-protein-coupled receptor GPR119 in a patient.

A further aim of the présent invention is to provide a pharmaceutical composition comprising at least one compound according to the invention.

A further aim of the présent invention is to provide a combination of at least one compound according to the invention with one or more additional therapeutic agents.

A further aim of the présent invention is to provide methods for the synthesis of the new compounds, in particular 2,3-dihydro-benzofuran-2-yl-piperidine dérivatives.

A further aim of the présent invention is to provide starting and/or intermediate compounds suitable in methods for the synthesis of the new compounds.

Further aims ofthe présent invention become apparent to the one skilled in the art by the description hereinbefore and in the following and by the examples.

Object of the Invention vY

It has now been found that the compounds according to the invention described in more detail hereinafter hâve surprising and particularly advantageous properties, and in particular as GPR119 agonists.

In a first aspect the invention thus relates to a compound of formula I

wherein

R¹ is selected from the group R¹-G1 consisting of a 5- or 6-membered heteroaromatîc ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S; and wherein optionally a second ring may be condensed to said heteroaromatîc ring, wherein said second ring is unsaturated or aromatic and 5- or 6-membered and may contain 1, 2 or 3 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -N(Rⁿ)-, -0(=0)-, -S(=O)- or -S(=O)2-, and wherein in said heteroaromatîc ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by Rⁿ, and wherein each of said heteroaromatîc ring and/or second ring independently of each other may be optionally substituted with one or more substituents selected from L^A; and wherein said heteroaromatîc ring or said second ring may be optionally substituted with a group R^c; and îA/

Rⁿ independently of each other is selected from the group R^N-G1 consisting of H, CM-alkyl, Ci^-alkyl-C(=O)-, and Ci^-alkyl-S(=O)₂-; and

A is selected from the group A-G1 consisting of a 1,2,3,6-tetrahydropyridin-

4- yl ring substituted at the N with Ci.4-alkyl-S(=O)₂-, a phenyl ring, and a

5- or 6-membered heteroaromatic ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S; and wherein optionally a second ring may be condensed to said phenyl ring or heteroaromatic ring, wherein said second ring is unsaturated or aromatic and 5- or 6-membered and may contain 1, 2 or 3 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -N(Rⁿ)-, -0(=0)-, -S(=O)- or-S(=O)₂-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said phenyl ring, heteroaromatic ring and/or second ring independently of each other may be optionally substituted with one or more substituents selected from L^A; and wherein said phenyl ring, heteroaromatic ring or second ring may be optionally substituted with a group T; and is selected from the group T-G1 consisting of F, Cl, Br, I, CN, OH, NO₂,

Ci-e-alkyl-, C_V6-alkenyl-, Ci.₆-alkynyl-, C₃.₆-cycloalkyl, Ci.₆-alkyl-O-, C₃.₆cycloalkyl-O-, Ci.₆-alkyl-S-, HO-C(=O)-, C^-alkyl-O-C^O)-, C_M-alkylC(=O)-, C₃.6-cycloalkyl-C(=O)-, Ci-4-alkyl-S(=O)-, Ci-₄-alkyl-S(=O)₂-,

R^NT2N-C(=O)(Rⁿ)N-, heterocyclyl, heterocyclyl-O-, aryl, aryl-O-, heteroaryl and heteroaryl-O-, wherein each alkyl, alkenyl, alkynyl, and cycloalkyl group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN, OH, Ci-₃-alkyl, C₃-6-cycloalkyl, C1.3- v/~~ r^nt1 alkyl-O-, R^NT1R^NT2N-, R^NT1R^NT2N-C(=O)-, Ci.₄-alkyl-S(=O)-, C_M-alkylS(=O)₂-, R^NT1R^NT2N-S(=O)2-, aryl, heteroaryl, and heterocyclyl, and wherein aryl dénotés phenyl or naphthyl, and wherein heteroaryl is a 5- or 6-membered aromatic ring which contains 1, 2, 3 or 4 heteroatoms independently of each other selected from N, O and S, wherein the H-atom in one or more NH groups may be optionally replaced by R^N; and wherein heterocyclyl is a 4- to 7-membered unsaturated or saturated carbocyclic ring in which 1 or 2 -CH₂-groups independently of each other are replaced by NRⁿ, O, -C(=O)-, S, -S(=O)- or-S(=O)₂-, and/or in which a -CH-group is replaced by N; and wherein each aryl, heteroaryl or heterocyclyl group may be optionally substituted with one or more substituents independently of each other selected from L^A; and is selected from the group R^NT1-G1 consisting of H, Cve-alkyl, C₃.₆cycloalkyl, Ci-e-alkyl-C(=O)-, Ci.₆-alkyl-S(=O)₂₎ heterocyclyl, aryl and heteroaryl, wherein each alkyl and cylcoalkyl group may be optionally substituted with one or more substituents independently of each other selected from the group consisting of F, OH, CN, Ci.₄-alkyl, Ci.₄-alkyl-O-, R^N2N, C-i-4-alkylS(=O)₂-, C3.6-cycloalkyl, heterocyclyl, phenyl and heteroaryl; and wherein heterocyclyl may be optionally substituted with one or more substituents independently of each other selected from F, CM-alkyl, R^N2N, OH and C^-alkyl-O-; and wherein heterocyclyl is a C4-7-cycloalkyl ring in which 1 or 2 -CH₂-groups_v7<

independently of each other are replaced by NRⁿ, O, C(=O), S, S(=O) or

S(=O)₂; and wherein aryl is phenyl or naphthyl; and wherein heteroaryl is a 5- or 6-membered aromatic ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S, wherein the H-atom in one or more NH groups may be optionally replaced by Rⁿ; and wherein aryl and heteroaryl may be optionally substituted with one or more substituents L^A; and

R^NT2 is selected from the group R^NT2-G1 consisting of H and Cve-alkyl; or

R^NT1 and R^NT2 are linked to form one group selected from the group R^NT1R^NT2-G1 consisting of a C3.5-alkylene group, wherein 1 or 2 -CH2-groups independently of each other are replaced by NRⁿ, O, C(=O), S, S(=O) or S(=O)2; and which may be optionally substituted with one or more substituents independently of each other selected from F, C-M-alkyl, (Rⁿ)₂N, OH and C_M-alkyl-O-;

L^a is selected from the group L^A-G1 consisting of F, Cl, Br, CN, OH, NO₂, Ci-

4-alkyl-, Ci.₄-alkyl-O-, (Rⁿ)2N-C(=O), (Rⁿ)2N-, and Ci.₄-alkyl-S(=O)₂-, wherein each alkyl group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN, OH and Ci-3-alkyl-O-; and

L^p is selected from the group L^p-G1 consisting of F and Cva-alkyl, wherein the alkyl group may be substituted with one or more F-atoms; and

L° is selected from the group L°-G1 consisting of F and C-|.₃-alkyl, wherein the alkyl group may be substituted with one or more F-atoms; and %a/

R^c is selected from the group R^c-G1 consisting of F, Cl, Br, I, CN, OH, NO₂,

Ci-6-alkyl-, Cvg-alkenyl-, Ci.₆-alkynyl-, Ca-e-cycloalkyl, Ci-e-alkyl-O-, C₃.₆cycloalkyl-O-, Ci.₆-alkyl-S-, HO-C(=O)-, Ci-e-alkyl-O-C(=O)-, C-M-alkylC(=O)-, C3-6-cycloalkyl-C(=0)-, C^-alkyl-S^O)-, Ci.₄-alkyl-S(=O)₂-, rNTIrNtz^ rNT1rNT2_n__C(=O)-, r^nt1r^NT2N-S(=O)₂-, R^NT1R^NT2N-C(=O)(Rⁿ)N-, heterocyclyl, heterocyclyl-O-, aryl, aryl-O-, heteroaryl and heteroaryl-O-, wherein each alkyl, alkenyl, alkynyl, and cycloalkyl group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN, OH, Ci-3-alkyl, Cs-e-cycloalkyl, C1-3alkyl-O-, R^NT1R^NT2N-, R^nt1R^NT2N-C(=O)-, Ci.4-alkyl-S(=O)-, C^-alkylS(=O)2-, R^NT1R^NT2N-S(=O)2-, aryl, heteroaryl, and heterocyclyl, and wherein aryl dénotés phenyl or naphthyl, and wherein heteroaryl is a 5- or 6-membered aromatic ring which contains 1, 2, 3 or 4 heteroatoms independently of each other selected from N, O and S, wherein the H-atom in one or more N H groups may be optionally replaced by R^N; and wherein heterocyclyl is a 4- to 7-membered unsaturated or saturated carbocyclic ring in which 1 or 2 -CH₂-groups independently of each other are replaced by NRⁿ, O, -C(=O)-, S, -S(=O)- or-S(=O)₂-, and/or in which a -CH-group is replaced by N; and wherein each aryl, heteroaryl or heterocyclyl group may be optionally substituted with one or more substituents independently of each other selected from l_^A; and

X¹, X², X³ are independently selected from the group X-G1 consisting of C(R²) and N, such that 0, 1 or 2 members of the group consisting of X¹, X², and X³ hâve the meaning N; and

R² is selected from the group R²-G1 consisting of H, F, Cl, CN, OH, Cmalkyl, C3-7-cycloalkyl-, F₂HC, F₃C, Ci.₄-alkyl-O-, F₂HC-O-, F3C-O- and C3.7cycloalkyl-O-; and n is an integer selected from 0, 1,2, 3 or 4; and m is an integer selected from 0, 1, or 2;

including anytautomers and stereoisomers thereof, or a sait thereof or a solvaté or hydrate thereof.

In a further aspect the présent invention relates to processes for preparing a compound of general formula I and to new intermediate compounds in these processes.

A further aspect of the invention relates to a sait of the compounds of general formula I according to this invention, in particular to a pharmaceutically acceptable sait thereof.

In a further aspect this invention relates to a pharmaceutical composition, comprising one or more compounds of general formula I or one or more pharmaceutically acceptable salts thereof according to the invention, optionally together with one or more inert carriers and/or diluents.

In a further aspect this invention relates to a method for treating diseases or conditions which are mediated by activating the G-protein-coupled receptor GPR119 in a patient in need thereof characterized in that a compound of general formula I or a pharmaceutically acceptable sait thereof is administered to the patient.

According to another aspect of the invention, there is provided a method for treating a metabolic disease or disorder in a patient in need thereof characterized in that a compound of general formula I or a pharmaceutically acceptable sait thereof is administered to the patient.

According to anotheraspect ofthe invention, there is provided the use of a compound of the general formula I or a pharmaceutically acceptable sait thereof for the manufacture of a médicament for a therapeutic method as described hereinbefore and hereinafter.

According to another aspect of the invention, there is provided a compound of the general formula I or a pharmaceutically acceptable sait thereof for use in a therapeutic method as described hereinbefore and hereinafter.

In a further aspect this invention relates to a method for treating a disease or condition mediated by the activation ofthe G-protein-coupled receptor GPR119 in a patient that includes the step of administering to the patient in need of such treatment a therapeutically effective amount of a compound of the general formula I or a pharmaceutically acceptable sait thereof in combination with a therapeutically effective amount of one or more additional therapeutic agents.

In a further aspect this invention relates to a use of a compound of the general formula I or a pharmaceutically acceptable sait thereof in combination with one or more additional therapeutic agents for the treatment of diseases or conditions which are mediated by the activation ofthe G-protein-coupled receptor GPR119.

In a further aspect this invention relates to a pharmaceutical composition which comprises a compound according to general formula I or a pharmaceutically acceptable sait thereof and one or more additional therapeutic agents, optionally together with one or more inert carriers and/or diluents. vt/

Other aspects of the invention become apparent to the one skilled in the art from the spécification and the experimental part as described hereinbefore and hereinafter.

Detailed Description

Unless otherwise stated, the groups, residues, and substituents, particularly A, R¹, R², T, Rⁿ, R^nt1, R^NT2, L^a, L^p, L^q, R^c, X¹, X², X³, n, m are defined as above and hereinafter. If residues, substituents, or groups occur several times in a compound, as for example R^N, l_^A, L^p or L^Q, they may hâve the same or different meanings. Some preferred meanings of individual groups and substituents of the compounds according to the invention will be given hereinafter. Any and each of these définitions may be combined with each other.

Rù

R¹-G1:

The group R¹ is preferably selected from the group R¹-G1 as defined hereinbefore and hereinafter.

R¹-G2:

According to one embodiment the group R¹ is selected from the group R¹-G2 consisting of a 5-membered heteroaromatic ring which contains 2 or 3 heteroatoms independently of each other selected from N, O and S and a 6membered heteroaromatic ring which contains 1 or 2 N atoms; and wherein optionally a second ring may be condensed to said 5- and 6-membered heteroaromatic rings, wherein said second ring is unsaturated or aromatic and 5or 6-membered and may contain 1 or 2 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH2-groups may be optionally replaced by -N(Rⁿ)-, -C(=O)- or -S(=O)2-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said heteroaromatic ring and/or second ring independently of ν'/ each other may be optionally substituted with one or two substituents selected from L^a; and wherein said heteroaromatic ring or said second ring may be optionally substituted with a group R^c.

R¹-G2a:

According to one embodiment the group R¹ is selected from the group R¹-G2a consisting of a 5-membered heteroaromatic ring which contains 2 or 3 heteroatoms independently of each other selected from N, O and S and a 6membered heteroaromatic ring which contains 1 or 2 N atoms;

wherein in said heteroaromatic ring the H-atom in one or more N H groups may be optionally replaced by R^N, and wherein said heteroaromatic ring may be optionally substituted with one or two substituents selected from L^A; and wherein said heteroaromatic ring may be optionally substituted with a group R^c.

R¹-G3:

According to one embodiment the group R¹ is selected from the group R¹-G3 consisting of:

N

N

N

N

wherein R^N is as defined hereinbefore and hereinafter, and wherein each ring may be optionally substituted with one substituent L^A and each group may be optionally substituted with one substituent R^c.

R¹-G3a:

According to one embodiment the group R¹ is selected from the group R¹-G3a consisting of:

Jl * hi »	Il »	/Sîl \ J * V J *— rr rr » »	-ά II *— V-N J	.f'S ,N'N tr rr » »
pN	/°'N JJ 1	_//N'° zS'N --< J--J 1 »	hr 1	•-O -o 1 1
-O \---fsj «	o 1	n=7 n=n 1 t	•-<O	f/ *—Ç N , N“/ and

wherein R^N is as defined hereinbefore and hereinafter, and wherein each group may be optionally substituted with one substituent L^A and one substituent R^c.

R¹-G4:

In another embodiment the group R¹ is selected from the group R¹-G4 consisting

» and

, wherein each ring may be optionally substituted with one substituent L^A and one substituent R^c.

R¹-G4a:

In another embodiment the group R¹ is selected from the group R¹-G4a consisting

each ring may be optionally substituted with one substituent R^c.

wherein

R¹-G5:

In another embodiment the group R¹ is selected from the group R¹-G5 consisting

, wherein each ring may be optionally substituted with one substituent R^c.

Rⁿ-G1:

The group R^N is preferably selected from the group R^N-G1 as defined hereinbefore and hereinafter.

Rⁿ-G2:

In another embodiment the group R^N is selected from the group R^N-G2 consisting of H, methyl, ethyl, isopropyl, methylcarbonyl, and methylsulfonyl.

Rⁿ-G3:

In another embodiment the group R^N is selected from the group R^N-G3 consisting of H, methyl, methylcarbonyl, and methylsulfonyl.

Rⁿ-G4:

In another embodiment the group R^N is selected from the group R^N-G4 consisting of H and C-i-3-alkyl.

R^N-G4a:

In another embodiment the group R^N is selected from the group R^N-G4a consisting of H and methyl.

R^N-G4b:

In another embodiment the group R^N is selected from the group R^N-G4b consisting of H.

A:

A-G1:

The group A is preferably selected from the group A-G1 as defined hereinbefore and hereinafter.

A-G2:

In one embodiment the group A is selected from the group A-G2 consisting of a phenyl ring, a 6-membered heteroaromatic ring which contains 1 or 2 N-atoms, and a 5-membered heteroaromatic ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S; and wherein optionally a second ring may be condensed to said phenyl ring or said heteroaromatic ring, wherein said second ring is unsaturated or aromatic and is 5- or 6-membered and may optionally contain 1 or 2 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH₂-groups may optionally be replaced by -N(Rⁿ)-, -C(=O)-, -S(=O)- or -S(=O)2-, and wherein in said heteroaromatic rings and/or said second rings the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said phenyl ring, heteroaromatic rings and second rings may be optionally substituted independently of each other with one or more substituents selected from L^A; and --16478 wherein said phenyl ring, heteroaromatic rings or second rings may be optionally substituted with a group T; and the group A-G2 further consists of 1,2,3,6-tetrahydropyridin-4-yl wherein the H of the NH group is replaced by Ci.4-alkyl-S(=O)₂-.

A-G2a:

In another embodiment the group A is selected from the group A-G2a consisting of a phenyl ring, a 6-membered heteroaromatic ring which contains 1 or 2 Natoms and a 5-membered heteroaromatic ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S; wherein said phenyl ring or heteroaromatic ring is substituted with a group T, and wherein said phenyl ring and heteroaromatic ring may be optionally substituted with one or more substituents independently of each other selected from L^A, wherein in said heteroaromatic rings the H-atom in one or more N H groups may be optionally replaced by R^N.

A-G2b:

In another embodiment the group A is selected from the group A-G2b consisting of a phenyl ring and a 5- or 6-membered heteroaromatic ring which contains 1 or 2 heteroatoms independently of each other selected from N, O or S; and wherein a second ring is condensed to said phenyl ring or said heteroaromatic ring, wherein said second ring is unsaturated or aromatic and is 5- or 6-membered and may optionally contain 1 or 2 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -N(Rⁿ)-, -C(=O)-, -S(=O)- or -S(:=O)2-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said phenyl ring, heteroaromatic ring and second ring may be optionally substituted with one or more substituents independently of each other selected from L^A; and wherein said phenyl ring, heteroaromatic ring or second ring may be optionally substituted with a group T.

A-G2c:

In another embodiment the group A is selected from the group A-G2c consisting of 1,2,3,6-tetrahydropyridin-4-yl wherein the H of the NH group is replaced by Ci.

₄-alkyl-S(=O)₂-.

A-G3:

In one embodiment the group A is selected from the group A-G3 consisting of the cyclic groups phenyl, pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl, isoxazolyl, oxazolyl, oxadiazolyl imidazolyl, pyrazolyl, thienyl and thiazolylring, and wherein optionally a second ring may be condensed to said cyclic groups, wherein said second ring is selected from the group consisting of cyclopentene, cyclohexene, dihydropyrrole, tetrahydropyridine, tetrahydropyrazine, dihydrooxazine, dihydrofuran, dihydropyran, [1,3]dioxol, dihydrodioxine, dihydropyrimidine, dihydropyrazine, dihydropyridazine, benzene, pyridine, pyrimidine, pyrazine, pyridazine, oxazole and thiazole, wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -C(=O)-, and wherein in said cyclic groups and/or second rings the H-atom in one or more -NH-groups may be replaced independently of each other by the substituent R^N, wherein each of the beforementioned rings may be optionally substituted with one or more substituents independently of each other selected from L^A, and wherein said cyclic group or second ring may be substituted with a group T; and the group A-G3 further encompasses 1,2,3,6-tetrahydropyridin-4-yl wherein the H of the NH group is replaced by Ci.3-alkyl“S(=O)₂-.

A-G3a:

In one embodiment the group A is selected from the group A-G3a consisting of a phenyl and a heteroaromatic carbocyclic ring selected from pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl, isoxazolyl, oxazolyl, oxadiazolyl, imidazolyl, pyrazolyl, thienyl and thiazolylring, wherein said phenyl and heteroaromatic rings may be optionally substituted with one or more substituents independently of each other selected from L^A, and wherein said phenyl or heteroaromatic ring is substituted with a group T.

A-G3b:

In one embodiment the group A is selected from the group A-G3b consisting of a phenyl and a heteroaromatic ring selected from pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl, isoxazolyl, oxazolyl, oxadiazolyl, imidazolyl, pyrazolyl, thienyl and thiazolyl ring, and wherein a second ring is condensed to said phenyl or heteroaromatic ring, wherein said second ring is selected from the group consisting of cyciopentene, cyclohexene, dihydropyrrole, tetrahydropyridine, tetrahydropyrazine, dihydrooxazine, dihydrofuran, dihydropyran, [1,3]dioxol, dihydrodioxine, dihydropyrimidine, dihydropyrazine, dihydropyridazine, benzene, pyridine, pyrimidine, pyrazine, pyridazine, oxazole and thiazole, wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -C(=O)-, and wherein in said heteroaromatic ring and/or second ring the H-atom in one or more -NH-groups may be replaced independently of each other by the substituent R^N, wherein each of the beforementioned rings may be optionally substituted with one or more substituents independently of each other selected from L^A, and wherein said phenyl ring, heteroaromatic ring or second ring may be optionally substituted with a group T.

A-G3c:

In another embodiment the group A is selected from the group A-G3c consisting of 1,2,3,6-tetrahydropyridin-4-yl wherein the H of the NH group is replaced by Ci.

₃-alkyl-S(=O)₂-. —

A-G3d:

In another embodiment the group A is selected from the group A-G3c consisting of 1,2,3,6-tetrahydropyridin-4-yl wherein the H ofthe NH group is replaced by CH₃-S(=O)₂-.

A-G4:

In one embodiment the group A is selected from the group A-G4 consisting of phenyl, pyridyl, pyrazinyl, pyridazinyl, pyrimidinyl, îsoxazolyl, oxazolyl, imidazolyl, pyrazolyl, thienyl, thiazolyl, [1,2,4]triazolo[1,5-a]pyndinyl, benzooxazolyl, benzothiazolyl, indan-1-onyl, indolyl, 2,3-dihydro-indolyl, quinoxalinyl, quinolinyl, 3H-quinazolin-4-onyl, 2,3-dihydro-benzo[1,4]dioxinyI, 3,4-dihydro-1 H-2-oxa-4a,9diaza-fluorenyl, isoindole-1,3-dionyl, 1,3-dihydro-indol-2-onyl, 1 H-indazolyl, indanyl, 2-oxo-2,3-dihydro-oxazolo[4,5-b]pyridinyl and isoxazolo[5,4-b]pyridinyl, wherein in the beforementioned groups in one or more -NH-groups the H-atom may be optionally replaced independently of each other by the substituent R^N, and wherein each ring may be optionally substituted with a group T and optionally with one or more substituents independently of each other selected from L^A, and the group A-G4 additionally consists of 1,2,3,6-tetrahydropyridin-4-yl wherein the H of the NH group is replaced by Ci-₃-alkyl-S(=O)₂-, preferably by CH3-S(=O)₂-.

A-G5:

In another embodiment the group A is selected from the group A-G5 consisting of:

N

N

N

N />

^N and

wherein in the above groups a H-atom in a -NH-group may be optionally replaced by the substituent R^N, and wherein each aromatic and heteroaromatic group is not substituted with a group T or is substituted with a group T, and each aromatic and heteroaromatic ring may be optionally substituted with one or more substituents independently of each other selected from L^A, and wherein the groups T and L^A are defined as hereinbefore and hereinafter.

A-G5a:

In another embodiment the group A is selected from the group A-G5a consisting of:

and

wherein the above-mentioned phenyl group is substutited with one Ci.₃-alkylS(=O)₂-, C₁.₃-alkyl-S(=O)2-CH₂- or -(CO)-NR^NT1R^NT2, wherein R^NT1 and R^NT2 are as defined hereinbefore and hereinafter;

preferably R^NT1 is Ci-₆-alkyl or tetrahydropyranyl, wherein the alkyl group may be optionally substituted with one CN, OH, OCH₃₁ tetrahydrofuranyl, oxazolyl, [1,4]-dioxanyl or pyridinyl; and

R^NT2 is H or methyl, in particular R^NT2 is H;

or R^NT1 and R^NT2 together with the N atom to which they are attached form an azetidinyl, pyrrolidinyl, piperidinyl or morpholinyl group, wherein each ofthe azetidinyl, pyrrolidinyl and piperidinyl groups may be optionally substituted with one or two substituents independently selected from the group consisting of F, OH, CH₃ and -OCH₃.

A-G5b:

In another embodiment the group A is selected from the group A-G5a, wherein the phenyl group is substituted in position 4.

A-G6:

In another embodiment the group A is selected from the group A-G6 consisting of:

N H

A-G6a:

In another embodiment the group A is selected from the group A-G6a consisting of:

A-G6b:

In another embodiment the group A is selected from the group A-G6b consisting of:

T

T-G1:

The group T is preferably selected from the group T-G1 as defined hereinbefore and hereinafter.

T-G2:

According to one embodiment the group T is selected from the group T-G2 consisting of F, Cl, Br, CN, OH, NO₂, C-M-alkyl-, Ci-4-alkyl-O-, Ci-4-alkyl-O-C(=O)-, Cw-alkyl-C(=O)-, Ci.₄-alkyl-S(=O), Ci.₄-alkyl-S(=O)₂. C₁.4-alkyl-S(=O)₂-C_M-alkyl-, R^NT1R^NT2N-C(=O)-, R^nt1R^NT2N-S(=O)2-, C1.4-alkyl-S(=O)2-(R^N)N-, R^NT1R^NT2N, RNTiRNT²N-C(=O)-Ci-4-alkyl-, wherein each alkyl-group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN , OH, aryl, heteroaryl, and heterocyclyl, wherein heteroaryl is selected from the group consisting of pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, pyrazolyl, imidazolyl, [1,2,4]triazolyl and tetrazolyl; and wherein heterocyclyl is azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl or morpholinyl, in which a -CH₂-group may be optionally replaced by a group selected from -C(=O)- and -S(=O)₂-, wherein heterocyclyl group may be optionally substituted with one or more substituents independently of each other selected from Ci-3-alkyl; and wherein phenyl and heteroaryl may be optionally substituted independently of each other with one or more substituents L^A.

T-G3:

According to another embodiment the group T is selected from the group T-G3 consisting of CN, C^-alkyl-S(=O)₂-CH₂ -, Ci.₄-alkyl-S(=O)₂, R^NT1R^NT2N-S(=O)2-, R^nt1R^NT2N-C(=O)-, C1_4-alkyl-S(=O)₂-(R^N)N-, and R^NT1R^NT2N-.

T-G4:

According to another embodiment the group T is selected from the group T-G4 consisting of Ci^-alkyl-S(=O)₂-CH₂-, C₁.4-alkyl-S(=O)₂ and R^NT1R^NT2N-C(=O)-. Examples of the group T-G4 are CH₃-S(=O)₂-CH₂-, and CH3-S(=O)₂-.

r^nt1

R^nt1-G1:

R^nt1 is preferably selected from the group R^NT1-G1 as defined hereinbefore and hereinafter.

R^NT1-G2:

In another embodiment R^NT1 is selected from the group R^NT1-G2 consisting of H, Ci-4-alkyl, 03-6-cycloalkyl, tetrahydropyranyl, wherein each alkyl and cylcoalkyl group may be optionally substituted with one substituent selected from the group consisting of F, CH3, OH, Ci.₃-alkyl-O-, (Rⁿ)2N, CN, tetrahydrofuranyl, 1,4-dioxinyl, oxazolyl, and pyridyl.

R^NT1-G3:

In another embodiment R^NT1 is selected from the group R^NT1-G3 consisting of H, C-i-4-alkyl and C₃.6-cycloalkyl, wherein each alkyl and cylcoalkyl group may be optionally substituted with one or two substituents independently of each other selected from the group consisting of F, CH₃, OH and Ci-₃-alkyl-O-.

R^NT1-G4:

In another embodiment R^NT1 is selected from the group R^NT1-G4 consisting of H and Ci-4-alkyl, wherein each alkyl and cycloalkyl group may be optionally substituted with one substituent selected from the group consisting of F, CH₃, OH and Ci.₃-alkyl-O-.

R^NT2

R^NT2-G1:

R^NT2 is preferably selected from the group R^NT2-G1 as defined hereinbefore and hereinafter.

R^NT2-G2:

In another embodiment R^NT2 is selected from the group R^NT2-G2 consisting of H and Ci-3-alkyl.

R^NT2

In another embodiment R^NT2 is selected from the group R^NT2-G3 consisting of H and methyl.

_RNT2

In another embodiment R^NT2 is selected from the group R^NT2-G4 consisting of H.

_rNT1_rNT2 _RNT1rNT2._g1;

According to one embodiment the groups R^NT1 and R^NT2 are linked and form a group which is selected from the group R^NT1R^NT2-G1 as defined hereinbefore and hereinafter.

_rnti_rnt2__G2;

According to another embodiment the groups R^NT1 and R^NT2 are linked and together with the N-atom to which they are attached form a group which is selected from the group R^NT1R^NT2-G2 consisting of azetidinyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, piperazin-2-onyl, N-Ci-3-alkyl-piperazinyl, NCi-3-alkyl-piperazin-2-onyl, and N-(Ci.₃-alkyl-C(=O))-piperazinyl, which may be optionally substituted with one or more substituents independently of each other selected from the group consisting of F, HO, Ci.₃-alkyl, Ci-₃-alkyl-O-, and (Rⁿ)2N.

_rnti_rnt2._G3:

According to another embodiment the groups R^NT1 and R^NT2 are linked and together with the N-atom to which they are attached form a group which is selected from the group R^NT1R^NT2-G3 consisting of azetidinyl, pyrrolidinyl, piperidinyl and morpholinyl, which may each be optionally substituted with one or two substituents independently of each other selected from the group consisting of F, OH, CH₃ and CH₃-O-,

Lù

L^a-G1:

The group L^A is preferably selected from the group L^a-G1 as defined hereinbefore and hereinafter.

L^a-G2:

In another embodiment the group L^A is selected from the group L^A-G2 consisting of F, Cl, Br, CN, OH, Ci-3-alkyl-, Ci-3-alkyl-O-, H₂N’, Ci.₃-alkyl-NH- and (C1-3alkyl^N-, wherein the Ci-₃-alkyl- and Ci-3-alkyl-O- group may be optionally substituted with one or more F-atoms.

L^a-G3:

In another embodiment the group L^A is selected from the group L^A-G3 consisting of F, Cl, C-M-alkyl- and CF₃.

r^:

R^c-G1:

The group R^c is preferably selected from the group R^c-G1 as defined hereinbefore and hereinafter.

R^c-G2:

According to one embodiment the group R^c is selected from the group R^c-G2 consisting of F, Cl, Br, I, CN, OH, Ci„6-alkyl-, Ci-6-alkenyl-, Ci.6-alkynyl-r C3-6cycloalkyl, Ci.6-alkyl-O-, C3.6-cycloalkyl-O-, Ci.6-alkyl-S-, Ci.6-alkyl-O-C(=O)-, C>4· alkyl-S(=O)-, Ci.4-alkyl-S(=O)-Ci.4-alkyl·, Ci.4-alkyi-S(=O)2-, Ci-4-alkyl-S(=O)2-Ci-4alkyl-, R^NT1R^NT2N-, R^NT1R^NT2N-CV3-alkyl-, R^NT1R^NT2N-C(=O)-, R^nt1R^NT2N-S(=O)2-, RNT1 rNT2n.S(=O)2_Ci 4-a|ky|_, RNT1 r^NT2N_c(=O)-Cv₄-alkyl-, heterocyclyl, heterocyciyl-O-, phenyl and heteroaryl, wherein each alkyl, alkenyl, alkynyl, and cycloalkyl group may be optionally substituted with one or more substituents îndependently of each other selected from F, Cl, CN, OH, Ci-3-alkyl, C₃.₆cycloalkyl, C-[.₃-alkyl-O-, phenyl, heteroaryl, and heterocyclyl, and wherein heteroaryl is selected from the group consisting of pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, pyrazolyl, imidazolyl, thiazolyl, and thienyl; and vx/ wherein heterocyclyl is selected from the group consisting of pyrrolidin-2-onyl, piperidin-2-onyl, piperazin-2-onyl, morpholinyl, morpholin-3-onyl, oxetanyl, tetrahydrofuranyl, and tetrahydropyranyl, each of which may be optionally substituted with one or two substituents independently of each other selected from

Ci.3-alkyl; and wherein phenyl and heteroaryl may be optionally substituted independently of each other with one or more substituents L^A.

R^c-G3:

According to one embodiment the group R^c is selected from the group R^c-G3 consisting of F, Cl, CN, CV6-alkyl-T C3-6-cycloalkyl, Cve-alkyl-O-, C3.6-cycloalkyl-O-, Ci-4-alkyl-S(=O)-, CM-alkyl-S(=O)2- R^NT1R^NT2N-, R^NT1R^NT2N-C^-alkyl-, RNT1_RNT2_N__C(=(·^.· _Rnti_rnt2_n._sî=Oj₂__ _rnti_rnt2_n__C(=Oj__Ci heterocyclyl, heterocyclyl-O-, phenyl and heteroaryl, wherein each alkyl and cycloalkyl group may be optionally substituted with one or more substituents independently of each other selected from F, HsC-, H3C-O-, phenyl, and heterocyclyl, and wherein heteroaryl is selected from the group consisting of pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, and thienyl; and wherein heterocyclyl is selected from the group consisting of oxetanyl, tetrahydrofuranyl and tetrahydropyranyl, each of which may be optionally substituted with one or two H3C- groups; and wherein phenyl and heteroaryl may be optionally substituted with one substituent L^a.

R^c-G4:

According to another embodiment the group R^c is selected from the group R^c-G4 consisting of F, Cl, Ci_₄-alkyl, F₃C-, C₃.₄-cycloalkyl, phenyl, wherein the phenyl ring v\/ may be monosubstituted with F, Cl, CH3, CF3, or OCH3 and the cycloalkyl groups may be monosubstituted with CH₃.

R^c-G4a:

According to another embodiment the group R^c is selected from the group R^cG4a consisting of F, Cl, C-M-alkyl, F₃C- and C₃.4-cycloalkyl, wherein the cycloalkyl groups may be monosubstituted with CH₃.

R^c-G4b:

According to another embodiment the group R^c is selected from the group R^cG4b consisting of F, Cl, C-M-alkyl, F₃C- and cyclopropyl, wherein the cyclopropyl group may be monosubstituted with CH₃.

R^c-G4c:

According to another embodiment the group R^c is selected from the group R^cG4a consisting of F, Cl, Ci-4-alkyl, F₃C-, C₃-4-cycloalkyl, and Ci-₃-alkyl-O-, wherein the cycloalkyl groups may be monosubstituted with CH₃.

R^c-G5:

According to another embodiment the group R^c is selected from the group R^c-G5 consisting of Ci.₄-alkyl, F3C-, cyclopropyl, cyclobutyl and phenyl, wherein the phenyl ring may be monosubstituted with F, Cl, CH₃, CF₃, or OCH₃.

R^c-G5a:

According to another embodiment the group R^c is selected from the group R^cG5a consisting of Ci-4-alkyl and F₃C-.

Preferred examples of the group R^c-G5a are ethyl, n-propyl and isopropyl.

R^c-G5b:

According to another embodiment the group R^c is selected from the group R^cG5a consisting of Ci-₃-alkyl, F₃C-, and H3C-O-.

X¹, X², X³

X-G1:

The group X¹, X², X³ is preferably selected from the group X-G1 as defined hereinbefore and hereinafter.

X-G2:

In another embodiment the group X¹, X², X³ is selected from the group X-G2 consisting of C(R²).

X-G3:

In another embodiment the group X¹, X², X³ is selected from the group X-G3 consisting of N and C(R²), such that 1 or 2 members of the group consisting of X¹, X² and X³ hâve the meaning N and the other members of said group hâve the meaning C(R²).

X-G4:

In another embodiment the group X¹, X², X³ is selected from the group X-G4 consisting of N and C(R²), such that 1 member of the group consisting of X¹, X² and X³ has the meaning N and the other members of said group hâve the meaning C(R²).

X-G4a:

In another embodiment X¹, X² and X³ are selected from the group X-G4a consisting of:

X¹ and X³ each being C(R²), and

X² having the meaning N.

X-G5:

In another embodiment the group X¹, X², X³ is selected from the group X-G5 consisting of N and C(R²), such that 2 members of the group consisting of X¹, X² and X³ hâve the meaning N and the other member of said group has the meaning C(R²).

e!

R²-G1:

The group R² is preferably selected from the group R²-G1 as defined hereinbefore and hereinafter.

R²-G2:

In another embodiment the group R² is selected from the group R²-G2 consisting of H, F, CN, OH, H₃C-, F₂HC, F₃C, H₃C-O-, F₂HC-O-, and F₃C-O-.

R²-G3:

In another embodiment the group R² is selected from the group R²-G3 consisting of H, F, and H₃C-.

R²-G4:

In another embodiment the group R² is selected from the group R²-G4 consisting of H.

LÙ

L^p-G1:

The group L^p is preferably selected from the group L^p-G1 as defined hereinbefore and hereinafter.

L^p-G2:

In another embodiment the group L^p is selected from the group L^p-G2 consisting of F and methyl.

L^q-G1:

The group L° is preferably selected from the group L^Q-G1 as defined hereinbefore and hereinafter.

L^Q-G2:

In another embodiment the group L^Q is selected from the group L^Q-G2 consisting of F and methyl,

Πϊ

The index n is an integer selected from 0,1, 2, 3 or 4.

According to one embodiment the index n is 0,1 or 2, in particular 0 or 1.

According to another embodiment the index n is 0.

m:

The index m is an integer selected from 0,1 or 2.

According to one embodiment the index m is 0, 1 or 2, in particular 0 or 1.

According to another embodiment the index m is 1.

According to another embodiment the index m is 0.

The following preferred embodiments of compounds of the formula I are described using generic formulas (1.1) to (I.7), wherein any tautomers and stereoisomers, solvatés, hydrates and salts thereof, in particular the pharmaceutically acceptable salts thereof, are encompassed.

R¹—N (1.1) (L^P)_n ^(L°^)m (I.2)

(I.3) (I.4) (I.5)

(I.6)

(l.6a)

(I.7)

wherein in each ofthe above formulas (1.1) to (I.7), the groups R¹, L^p, L^Q, n, m and A are defined as hereinbefore and hereinafter.

Further preferred embodiments of compounds of the formula I are described by generic formulas (I.R) and (I.S), wherein any tautomers and stereoisomers, solvatés, hydrates and salts thereof, in particular the pharmaceutically acceptable salts thereof, are encompassed.

(I.R) (I.S)

wherein in each ofthe above formulas (I.R) and (I.S), the groups R¹, L^p, L^Q, n, m, X¹, X², X³, and A are defined as hereinbefore and hereinafter.

Examples of preferred subgeneric embodiments according to the présent invention are set forth in the following table, wherein each substituent group of each embodiment is defined according to the définitions set forth hereinbefore and wherein ail other substituents of the formula I are defined according to the 10 définitions set forth hereinbefore:

Embodiment	Formula	R1-	A-
E-1	I	R1-G1	A-G1
E-2	I	R1-G2	A-G2a
E-3	I	R1-G2	A-G2b
E-4	I	R1-G2	A-G4
E-5	I	R1-G2	A-G5
E-6	I.R	R1-G1	A-G1
E-7	I.R	R1-G2	A-G2a
E-8	I.R	R1-G2	A-G2b
E-9	I.R	R1-G2	A-G4
E-10	I.R	R1-G2	A-G5
E-11	I.S	R1-G1	A-G1

Embodiment	Formula	R1-	A-
E-12	I.S	R1-G2	A-G2a
E-13	I.S	R1-G2	A-G2b
E-14	LS	R1-G2	A-G4
E-15	I.S	R1-G2	A-G5
E-16	1.1	R1-G1	A-G1
E-17	1.1	R1-G2	A-G2a
E-18	1.1	R1-G2	A-G2b
E-19	1.1	R1-G2	A-G4
E-20	1.1	R1-G2	A-G5
E-21	I.2	R1-G1	A-G1
E-22	I.2	R1-G2	A-G2a
E-23	I.2	R1-G2	A-G2b
E-24	I.2	R1-G2	A-G4
E-25	I.2	R1-G2	A-G5
E-26	I.3	R1-G1	A-G1
E-27	I.3	R1-G2	A-G2a
E-28	I.3	R1-G2	A-G2b
E-29	I.3	R1-G2	A-G4
E-30	I.3	R1-G2	A-G5
E-31	I.4	R1-G1	A-G1
E-32	I.4	R1-G2	A-G2a
E-33	I.4	R1-G2	A-G2b
E-34	I.4	R1-G2	A-G4
E-35	I.4	R1-G2	A-G5
E-36	I.5	R1-G1	A-G1
E-37	I.5	R1-G2	A-G2a
E-38	I.5	R1-G2	A-G2b
E-39	I.5	R1-G2	A-G4
E-40	I.5	R1-G2	A-G5
E-41	I.6	R1-G1	A-G1
E-42	I.6	R1-G2	A-G2a

Embodiment	Formula	R1-	A-
E-43	I.6	R1-G2	A-G2b
E-44	I.6	R1-G2	A-G4
E-45	I.6	R1-G2	A-G5
E-46	I.7	R1-G1	A-G1
E-47	I.7	R1-G2	A-G2a
E-48	I.7	R1-G2	A-G2b
E-49	I.7	R1-G2	A-G4
E-50	I.7	R1-G2	A-G5

Preferred are those compounds of formula I, wherein

X¹ is CH;

X² is CH or N;

X³ is CH;

R¹ is selected from the group consisting of:

wherein each ring may be optionally substituted with one F and/or with one substituent R^c;

R^c is selected from the group consisting of F, Cl, Ci.₄-alkyl, F₃C- and cyclopropyl, wherein the cyclopropyl group may be monosubstituted with CK₃;

A is selected from the group consisting of:

L^q is CH₃;

n is 0; j'j''' m is 0 or 1;

and the pharmaceutically acceptable salts thereof.

More preferred are those compounds of formula I, wherein

X¹ isCH;

X² is N;

X³ is CH;

R¹ is selected from the group consisting of:

wherein each ring may be optionally substituted with one F and/or with one substituent R^c;

R^c is selected from the group consisting of F, Cl, C-M-alkyl, F₃C- and cyclopropyl, wherein the cyclopropyl group may be monosubstituted with CH₃;

A is selected from the group consisting of:

o and

L^q is CH₃;

n is 0;

m is 0 or 1;

and the pharmaceutically acceptable salts thereof.

Particularly preferred compounds, including their tautomers and stereoisomers, the salts thereof, or any solvatés or hydrates thereof, are described in the experimental section hereinafter.

The following compounds are mentioned as examples of compounds according to the invention:

Example

O

Ο including any tautomers and stereoisomers thereof, or a sait thereof or a solvaté or hydrate thereof.

The compounds according to the invention and their intermediates may be obtained using methods of synthesis which are known to the one skilled in the art and described in the literature of organic synthesis. Preferably the compounds are obtained analogously to the methods of préparation explained more fully hereinafter, in particular as described in the experimental section. In some cases the sequence adopted in carrying out the reaction schemes may be varied. Variants of these reactions that are known to the skilled man but are not described in detail here may also be used. The general processes for preparing the compounds according to the invention will become apparent to the skilled man on studying the schemes that follow. Starting compounds are commercially available or may be prepared by methods that are described in the literature or herein, or may be prepared in an analogous or similar manner. Before the reaction is carried out any corresponding functional groups in the compounds may be protected using conventional protecting groups. These protecting groups may be cleaved again at a suitable stage within the reaction sequence using methods familiarto the skilled man.

Compounds of the invention I are accessible using the synthetic route sketched in Scheme 1; R¹, L^p, η, X¹, X², X³, and A hâve the meanings as defined hereinbefore and hereinafter. Starting with compound 1 the target compounds are obtained upon partial réduction of the benzofuran. The reaction is preferably conducted with hydrogen as the reducing agent in the presence of a transition métal catalyst. Suited transition metals may be derived from Ni, Pd, Pt, Ir, and Rh, such as Raney nickel, Pd on carbon, Pt on carbon, Rh on carbon, PtO₂, and Rh₂C>3. The réduction is preferably carried out in tetrahydrofuran, acetone, ethyl acetate, alcohol, e.g. methanol, éthanol, or isopropanol, acetic acid, or mixtures thereof, at hydrogen pressures of 1 to 100 bar, at 0 to 120 °C. Alternatively, formic acid or a formate instead of hydrogen may be used as reducing agent.

The réduction may also be accomplished with a silane or sodium amalgam as reducing agent. Réduction using a silane is for example conducted with triethylsilane and trifluoroacetic acid in dichloromethane, chloroform, acetonitrile, mixtures thereof, or without a solvent in trifluoroacetic acid, at -20 to 120 °C. Sodium amalgam is frequently employed in an aqueous solution with sodium hydroxide or sodium bicarbonate.

Scheme 1

Compound 1, in turn, may be obtained from compound 4, bearing two replaceable halogen or pseudo-halogen groups, as described in Scheme 2; R¹, L^p, η, X¹, X², X³, and A hâve the meanings as defined hereinbefore and hereinafter. Depending on the reactivity of the two carbon atoms bearing the halogen or pseudo-halogen groups, the two coupling partners, 6 and 5, are introduced following the sequence depicted on the top or bottom of the scheme. Both residues are preferably attached via a transition métal catalyzed reaction, preferably mediated by a palladium, nickel, copper, or iron species. The active catalyst may be derived from an elemental form of the transition métal, such as palladium on carbon or nanoparticles of iron or palladium, or a sait of the transition métal, such as fluoride, chloride, bromide, acetate, triflate, or trifluoroacetate, which are preferably combined with ligands, such as phosphines, e.g. tri-tertbutylphosphine, tricyclohexylphosphine, optionally substituted biphenyldicyclohexyl-phosphines, optionally substituted biphenyl-di-tert-butyl-phosphines, 1,T-bis(diphenylphosphino)-ferrocene, triphenylphosphine, tritolylphosphine, or trifurylphosphine, phosphites, 1,3-disubstituted imidazole carbenes, 1,3disubstituted imidazolidine carbenes, dibenzylideneacetone, allyl, or nitrites. A-M is preferably a boronic acid, trifluoroborate, boronic ester, zinc halide, or magnésium halide of A and alkyne 5 is preferably used as is or zinc acetylide. Depending on the nucleophiles the reactions are preferably conducted in benzene, toluene, ether, tetrahydrofuran, 1,2-dimethoxyethane, 1,4-dioxane, N,N dimethylformamide, Ν,Ν-dimethylacetamide, N-methylpyrrolidinone, alcohol, water, or mixtures thereof, at -10 to 160 °C. Additives such as halide salts, e.g. lithium chloride, potassium fluoride, tetrabutylammonium fluoride, hydroxide sources, such as potassium hydroxide, potassium carbonate, amines, such as triethylamine, diisopropylamine, and ethyldiisopropylamine, silver salts, such as silver oxide or triflate, and/or copper salts, such as copper iodide or chloride or copper thiophene-2-carboxylate, may be bénéficiai or even essential for the reaction to proceed. The conditions for the coupling of alkyne 5 with one of the electrophiles, 2 or 4, may bring about the subséquent cyclization as well and thus provide the benzofuran. For instance, with Pd(PPh3)2Cl2, Cul, and triethylamine in Ν,Ν-dimethylformamide at 20 to 140 °C the benzofuran may be obtained directly. If the intermediate alkyne is obtained the benzofuran may be formed in a separate step using, for example, Bu₄NF in tetrahydrofuran at 50 to 70 °C, NaOH in aqueous solution at elevated température, Cul or CuCN, optionally in the presence of NEt₃, in Ν,Ν-dimethylformamide at elevated température, AuCI(PPh₃) and AgOSO2CF₃ in CH₂CI₂ or tetrahydrofuran, AgOSO₂CF₃, optionally in the presence of trifluoroacetic acid, in CH₂CI₂, Pd, e.g. PdCl2, or other transition metals such as Rh. The benzofuran may also be assembled from a constellation in which the oxygen to cyclize (oxygen at the carbon atom next to the carbon atom bearing the alkynyl group) is embedded in an amide group of an azaheterocyclic group provided that the additional group on the amide N is cleavable under the reaction conditions (see e.g. Synthesis 2007, 3117).

The reactivities of the reaction partners (reacting carbons) described may be reversed, i.e. compounds 2, 3, and 4 are the nucleophile bearing M and compounds 5 and 6 are the electrophile bearing Hal¹ or Hal², providing the same products under the same or similar conditions.

Scheme 2 \a/

R¹’ = R¹, protective group, e.g., -CO_z'Bu

Hal¹, Hal² = halogen or pseudohalogen, e.g., Cl, Br, I, OSO₂CF₃, OSO₂Me, OSO₂aryl

M = métal residue, e.g., B(OH)₂, BF₃K, B(OCMe₂CMe₂O), ZnCI/Br/l, MgCI/Br/l

Another viable route to synthesize compounds of the invention employs benzofuran dérivative 7 as origin (Scheme 3); R¹, L^p, η, X¹, X², X³, and A hâve the meanings as defined hereinbefore and hereinafter. Compound 7 and piperidine 11 are preferably combined by a transition métal catalyzed process as described above for Scheme 2. The reactivity of the 2-position of the benzofuran 7 détermines the suîted piperidine 11 for the coupling reaction. Benzofurans bearing Cl, Br, or I at the 2-position are preferably matched with, e.g., tetrahydropyridines bearing for Z B(OH)₂, B(OCMe₂CMe2O), or BF3K. Reversing the reactivity of 7, i.e.

is the nucleophilic partner bearing M, e.g. B(OH)₂ or B(OCMe2CMe2O), demande a piperidine of opposite reactivity, i.e. tetrahydropyridines bearing for Z,

e.g., OSO2CF3 or Cl. Moreover, piperidin-4-ones (Z = =0) may be coupled with electrophilic benzofurans 7 (Y = Cl, Br, I) using tosylhydrazone, a base such as

LiOtBu, and a Pd catalyst in a solvent such as 1,4-dioxane (see e.g. Chem. Eur. J. >a/

2008, 14, 4792-5, and Org. Lett. 2010, 12, 4042-5, and references quoted therein). The additional double-bond in the product due to the use of a tetrahydropyridine may be reduced along with the benzofuran in the next reaction step as described above for Scheme 1. Halogénation with Cl, Br, or I of compound 9 delivers compound 10. Chlorination is accomplished with, for example, N-chlorosuccinimide, chlorine, or sulfuryl chloride. N-chlorosuccinimide is preferably used in the presence of a Lewis acid, e.g. ZrCLi or HCI, in dichloromethane, acetonitrile, Ν,Ν-dimethylformamide, methanol, water, oracetic acid; chlorine is preferably employed in chloroform oracetic acid, and sulfuryl chloride in dichloromethane and chloroform. Bromination is preferably achieved using bromine or N-bromosuccinimide in dichloromethane, acetonitrile, or acetic acid, optionally in the presence of a Lewis acid, lodine may be introduced with,

e.g., iodine combined with silver nitrate, iodine in sulfuric acid, N-iodosuccinimide combined with indium triflate, or iodine chloride in acetic acid or dichloromethane. The concluding step in Scheme 3, transition métal catalyzed coupling of 10 and 6, may be carried out in analogy to the proceeding described above.

Scheme 3

R¹' = R¹, protective group, e.g., -CO₂'Bu

Hal = Cl, Br, I

M = métal residue, e.g., B(OH)₂, B(OCMe₂CMe₂O), BF₃K, ZnCI/Br/l, MgCI/Br/l

Y = e.g., Hal, OSO₂CF₃, OSO₂Me, OSO_zPh, M, H

Z = e.g., Hal. OSO₂CF₃, M, =O

----= single or double bond 'Λ/'

I'

Scheme 4 shows another way of synthesis of compounds of the invention; R¹, L^p, L°, η, X¹, X², X³, and A hâve the meanings as defined hereinbefore and hereinafter. The sequence commences with réduction of ketone 12 to obtain alcohol 13. The réduction is preferably conducted with a complex métal hydride, such as sodium borohydride, lithium borohydride, lithium triethylborohydride, diisobutylaluminum hydride, or lithium aluminum hydride. Sodium borohydride is usually used in aqueous or alcoholic solutions at -20 to 100 °C, while the other reagents are preferably employed in dichloromethane, 1,2-dichloroethane, hexanes, ether, 1,4-dioxane, tetrahydrofuran, N-methylpyrrolidone, benzene, toluene, or mixtures thereof, at -80 to 60 °C. The réduction may also be conducted in a stereoselective fashion to access only one enantiomer using, e.g., the conditions of the Corey-Bakshi-Shibata (CBS) réduction (also called CoreyItsuno réduction).

Intramolecular substitution of the leaving group LG with oxygen provides target compound I”. For LG equals F, SO₂CM-alkyl, SO₂-aryl, or NO₂, the reaction is preferably carried out in the presence of a base, such as NaH, CaH2, BuLi, KO'Bu, or KOH, in toluene, tetrahydrofuran, 1,4-dioxane, Ν,Ν-dimethylformamide, N,Ndimethylacetamide, N-methylpyrrolidone, or mixtures thereof, at 20 to 200 °C. For LG is Cl, Br, I, the reaction is preferably conducted in the presence of a transition métal catalyst, such as a Pd or Cu species. ^/~

Scheme 4

LG = leaving group, e.g., F, Cl, Br, I, OSO₂C_M-alkyl, SO₂-aryl, NO₂ R^z = A or group that allows introduction of A, e.g., as described above R¹' = R¹, protective group, e.g., -CO₂'Bu L^Q' = L^Q, H

The dihydrofuran ring may also be formed from compound 13’, bearing an additional hydroxy group on the aromatic ring. Intramolecular substitution ofthe aliphatic OH group with the aromatic O group may be accomplished using a phosphine and an azodicarboxylic ester or amide in tetrahydrofuran, 1,4-dioxane, diethyl ether, toluene, benzene, dichloromethane, or mixtures thereof at -30 to 100 °C (Mitsunobu reaction). Triphenylphosphine or tributylphosphine combined with dimethyl azodicarboxylate, diethyl azodicarboxylate, diisopropyl azodicarboxylate, di-(4-chlorobenzyl) azodicarboxylate, dibenzyl azodicarboxylate, di-tert-butyl azodicarboxylate, azodicarboxylic acid bis-(dimethylamide), azodicarboxylic acid dipiperidide, or azodicarboxylic acid dimorpholide are common combinations for this transformation. Alternatively, the aliphatic OH group may be transformed into a leaving group, such as Cl, Br, I, OSO₂CH₃, and OSO2ph, and then displaced with the aromatic O under basic conditions. Suited bases may be, for instance, carbonates, e.g. CS2CO3 and K2CO3, hydrides, e.g. NaH, alcoholates, e.g. NaOMe and KO^fBu, hydroxides, e.g. KOH and NaOH, that are preferably employed in toluene, tetrahydrofuran, Ν,Ν-dimethylformamide, N,Ndimethylacetamide, N-methylpyrrolidinone, dimethyl sulfoxide, alcohol, water, and mixtures thereof. The reaction may be carried out such that the aliphatic hydroxy group is subtituted with complété inversion of configuration delivering an vv16478 enantiomerically enriched or pure product provided an enantiomericaliy enriched or pure starting compound is used.

Scheme 5

R^r = R¹, protective group, e.g., -CO₂'Bu R^z = A or group that allows introduction of A, e.g., as described above

Intermediate 12 may be accessed as delineated in Scheme 6; R¹, L^p, L°, η, X¹, X², X³, and A have the meanings as defined hereinbefore and hereinafter. A carboxylic acid dérivative 14 can be merged with an aromatic compound 15, that bears an anionic carbon center attached to the aromatic ring, to provide intermediate 12’ (route a.). Suited carboxylic acid dérivatives may be e.g. carboxylic halides, carboxylic esters, carboxylic anhydrides, and carboxylic amides, while suited nucleophile precursors 15 preferably bear an electronwithdrawing group (EWG) at the carbon center to generate the négative charge more easily; preferred EWG are carboxylic esters and cyano. The reaction is mediated by a base that deprotonates compound 15 to generate the anion which, in turn, adds to the carboxylic function of 14 to give 12’; the anion generating step may be carried out in the presence or prior to the addition of compound 14. Most preferred bases are selected from alcoholates, e.g. KO'Bu and NaOMe, amines,

e.g. triethylamine and 1,8-diazabicyclo[5.4.0]undec-7-ene, carbonates, e.g. CS2CO3 and K2CO3, hydroxides, e.g. NaOH and KOH, and amides, e.g.

LiN(SiMe₃)₂ and LiN'Pr₂₁ that, depending on their reactivity and compatibility, may be used in solvents such as toluene, tetrahydrofuran, 1,4-dioxane, N,Ndimethylformamide, Ν,Ν-dimethylacetamide, N-methylpyrrolidinone, diméthyl sulfoxide, alcohol, or mixtures thereof. For example, a compound 14 bearing an ester function (X = O-C^-alkyl) may be combined with a compound 15 bearing a cyano or ester group (EWG = CN or C(=O)OC-|.₄-alkyl) using KO^fBu or NaOEt as base and tetrahydrofuran, N-methylpyrrolidinon, or éthanol as solvent. The product 12’ may be transformed into intermediate 12 by hydrolysis of the ester or cyano group followed by décarboxylation of the resulting carboxylic acid function. EWG groups such as nitro or sulfonyl can be removed as well.

Combination of compounds 16 and 17 is another way of synthesis for intermediate 12 (route b.). Depending on the reactivity ofthe coupling partners, the reaction is best conducted in the presence of a transition métal catalyst or without an additive. For example, compound 16 bearing a boronic acid (M = B(OH)₂) and compound 17 having a carboxylic chloride (X = Cl) may be coupled using a Pd catalyst, e.g. Pd(PPh3)₄, and a base, e.g. K3PO₄, in a solvent, e.g. toluene or 1,4-doxane, at 60 to 120 °C. A compound 16 with M = Li or MgCI may be matched with an electrophile 17 bearing a carboxamide group (X = N(OMe)Me). The reaction is commonly conducted in tetrahydrofuran, 1,4-dioxane, ether, toluene, or mixtures thereof, at -70 to 40 ’C, optionally in the presence of an additive such as CeCl3. Compound 12 may be converted to intermediate 12 by réduction ofthe double bond with hydrogen or a formate in the presence of a transition métal, e.g. Pd on carbon, or a hydride, e.g. [CuH(PPh₃)]₆.

Scheme 6

EWG

R^z

R¹' = R\ protective group, e.g., -CO₂'Bu

R^z = A or group that allows introduction of A, e.g., as described above

L^Q' = H, L^Q

EWG = H or électron withdrawing group, e.g., CO₂C_M-alkyl, CN, SO₂C_lJ(-alkyl, NO₂ LG = leaving group, e.g., F, Cl, Br, I, SO₂C_lJ(-alkyl, SO₂-aryl, NO₂

M = métal residue, e.g., B(OH)₂, BF₃K, B(OCMe₂CMe₂O), ZnCI/Br/l, MgCI/Br/l, CeCI₂ X = leaving group, e.g., Cl, OC_M-alkyl, N(OMe)Me

The general way of attaching residue R¹ to the N atom of the piperidine of the compounds of the invention or an intermediate towards them is sketched in Scheme 7; R¹, L^p, and n hâve the meanings as defined hereinbefore and hereinafter. The reaction may be conducted as a classical nucleophilic substitution on a heteroaromatic bearing a leaving group, such as F, Cl, Br, SOaCM-alkyl, SO₂aryl, and NO₂. The reaction partners are preferably coupled in the presence of a mild base, e.g. Na₂CO₃, K₂CO₃, or Cs₂CO₃, pyridine, 4dimethylaminopyridine, triethylamine, ethyldiisopropylamine, 1,8diazabicylo[5.4.0]undec-7-ene, in toluene, tetrahydrofuran, 1,4-dioxane, 1,2dimethoxyethane, acetonitrile, N.N-dimethylformamide, Ν,Ν-dimethylacetamide, N-methylpyrrolidinone, water, methanol, éthanol, isopropanol, dimethyl sulfoxide, or mixtures thereof, at 20 to 220 °C by conventional or microwave heating. Alternatively, the piperidine 18 may be transformed into the corresponding métal piperidide by deprotonation with a strong base, e.g. butyl lithium, NaH, or KH, priorto the addition ofthe electrophile 19,

In certain cases the use of transition metals as catalysts for the coupling may be bénéficiai or even essential. The leaving group X in compound 19 is then preferably Cl, Br, I, OSO₂CH₃, OS0₂tolyl, and OSO₂CF₃. The reactions are preferably conducted with a transition métal derived catalyst which is preferably based on copper or palladium. The catalyst may be an elemental form of the transition métal, such as palladium on charcoal or nanoparticles of palladium, a sait ofthe transition métal, such as CuCI, CuBr, Cul, Cu(O₃SCF₃)₂, Cu(O₂CCH₃)₂, PdCI₂, PdBr₂, Pd(O₂CCH₃)₂, and Pd(O₂CCF₃)₂, or a complex ofthe transition métal, such Pd₂(dibenzylideneacetone)₃, all of which may optionally be combined with additional ligands, such as phosphines, e.g. triphenylphosphine, tritolylphosphine, tri-cyclohexylphosphine, tri-tert-butylphosphine, 1,Tbis(diphenylphosphino)ferrocene, optionally substituted biphenyl-di-tertbutylphosphines or biphenyl-dicyclohexyl-phosphines, 2,2'bis(diphenylphosphinyl)-1,T-binaphthyl, 1,3-disubstituted imidazole or imidazolidine carbenes, phosphites, 1,3-diketones, nitriles, oralkenes. The coupling reaction is preferably conducted in the presence of a base, such as NaOfBu, KOfBu, LiN(SiMe₃)₂, K₂CO₃, Cs₂CO₃, or K₃PO₄, in toluene, benzene, tetrahydrofurane, 1,4-dioxane, 1,2-dimethoxyethane, N.N-dimethylformamide,

Ν,Ν-dimethylacetamide, N-methylpyrrolidinone, dimethyl sulfoxide, /BuOH, or mixtures thereof, at 0 to 180 °C.

Alternatively, particular residues R¹ such as [1,2,4]oxadiazoles and [1,2,4]triazoles may be assembled from the corresponding cyanamide of compound 18 and Nhydroxyamidine or N-aminoamidine, respectively, as described in the experimental part.

Rg = group that allows attachment of or is missing residue to obtain compounds of general formula I, e.g., see respective compounds outlined above

X = leaving group, e.g„ F, Cl, Br, I, OSO₂CF₃, OSC^C^-alkyl, OSO₂-aryl, SOjC^-alkyl, NO₂ — = single or double bond

The synthetic routes presented may rely on the use of protecting groups. For example, potentially reactive groups présent, such as hydroxy, carbonyl, carboxy, amino, alkylamino, or imino, may be protected during the reaction by conventional protecting groups which are cleaved again after the reaction. Suitable protecting groups for the respective functionalities and their removal are well known to the one skilled in the art and are described in the literature of organic synthesis.

The compounds of general formula I may be resolved into their enantiomers and/or diastereomers as mentîoned before. Thus, for example, cis/trans mixtures may be resolved into their cis and trans isomers and racemic compounds may be separated into their enantiomers.

The cis/trans mixtures may be resolved, for example, by chromatography into the cis and trans isomers thereof. The compounds of general formula I which occur as racemates may be separated by methods known per se into their optical antipodes and diastereomeric mixtures of compounds of general formula I may be resolved into their diastereomers by taking advantage of their different physicochemical properties using methods known perse, e.g. chromatography and/or fractional crystallization; if the compounds obtained thereafter are racemates, they may be resolved into the enantiomers as mentioned above.

The racemates are preferably resolved by column chromatography on chiral phases or by crystallization from an optically active solvent or by reacting with an optically active substance which forms salts or dérivatives such as esters or amides with the racemic compound. Salts may be formed with enantiomerically pure acids for basic compounds and with enantiomerically pure bases for acidic compounds. Diastereomeric dérivatives are formed with enantiomerically pure auxiliary compounds, e.g. acids, their activated dérivatives, or alcohols. Séparation of the diastereomeric mixture of salts or dérivatives thus obtained may be achieved by taking advantage of their different physico-chemical properties,

e.g. différences in solubility; the free antipodes may be released from the pure diastereomeric salts or dérivatives by the action of suitable agents. Optically active acids in common use for such a purpose are e.g. the D- and L-forms of tartane acid, dibenzoyltartaric acid, dîtoluoyltartaric acid, malic acid, mandelic acid, camphorsulfonic acid, glutamic acid, aspartic acid, or quinte acid. Optically active alcohols applicable as auxiliary residues may be, for example, (+) or (-)-menthol and optically active acyl groups in amides may be, for example, (+)- or (-)-menthyloxycarbonyl.

As mentioned above, the compounds of formula I may be converted into salts, particularly for pharmaceutical use into the pharmaceutically acceptable salts. As used herein, pharmaceutically acceptable salts refer to dérivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof.

The compounds according to the invention are advantageously also obtainable using the methods described in the examples that follow, which may also be combined for this purpose with methods known to the skilled man from the literature.

Terms and définitions

Terms not specifically defined herein should be given the meanings that would be given to them by one of skill in the art in light of the disclosure and the context. As used in the spécification, however, unless specifîed to the contrary, the following terms hâve the meaning indicated and the following conventions are adhered to.

The terms compound(s) according to this invention, compound(s) of formula (I), compound(s) of the invention and the like dénoté the compounds of the formula (I) according to the présent invention încluding their tautomers, stereoisomers and mixtures thereof and the salts thereof, in particular the pharmaceutically acceptable salts thereof, and the solvatés and hydrates of such compounds, încluding the solvatés and hydrates of such tautomers, stereoisomers and salts thereof.

The terms treatment and treating embraces both preventative, i.e. prophylactic, or therapeutic, i.e. curative and/or palliative, treatment. Thus the terms treatment and treating comprise therapeutic treatment of patients having already developed said condition, in particular in manifest form. Therapeutic treatment may be symptomatic treatment in order to relieve the symptoms of the spécifie indication or causal treatment in order to reverse or partially reverse the conditions of the indication orto stop or slow down progression of the disease. Thus the compositions and methods of the présent invention may be used for instance as therapeutic treatment over a period of time as well as for chronic therapy. In addition the terms treatment and treating comprise prophylactic treatment, i.e. a treatment of patients at risk to develop a condition mentioned hereinbefore, thus reducing said risk.

When this invention refers to patients requiring treatment, it relates primarily to treatment in mammals, in particular humans.

The term therapeutically effective amount means an amount of a compound of the présent invention that (i) treats or prevents the particular disease or condition, (ii) atténuâtes, améliorâtes, or éliminâtes one or more symptoms of the particular disease or condition, or (iii) prevents or delays the onset of one or more symptoms ofthe particular disease or condition described herein.

The terms modulated or modulating, or modulate(s), as used herein, unless otherwise indicated, refers to the activation ofthe G-protein-coupled receptor GPR119 with one or more compounds of the présent invention.

The terms mediated or mediating or médiate, as used herein, unless otherwise indicated, refers to the (i) treatment, including prévention ofthe particular disease or condition, (ii) atténuation, amelioration, or élimination of one or more symptoms of the particular disease or condition, or (iii) prévention or delay of the onset of one or more symptoms of the particular disease or condition described herein.

The term substituted as used herein, means that any one or more hydrogens on the designated atom, radical or moiety is replaced with a sélection from the indicated group, provided that the atom's normal valence is not exceeded, and that the substitution results in an acceptably stable compound.

In the groups, radicals, or moieties defined below, the number of carbon atoms is often specified preceding the group, for example, Cve-alkyl means an alkyl group or radical having 1 to 6 carbon atoms. In general, for groups comprising two or more subgroups, the last named subgroup is the radical attachment point, for example, the substituent aryl-Cvs-alkyl- means an aryl group which is bound to a Cva-alkyl-group, the latter of which is bound to the core or to the group to which the substituent is attached.

In case a compound ofthe présent invention is depicted in form of a chemical name and as a formula in case of any discrepancy the formula shall prevail.

An asterisk is may be used in sub-formulas to indicate the bond which is connected to the core molécule as defined. ka/^-—

The numération of the atoms of a substituent starts with the atom which is closest to the core or to the group to which the substituent is attached.

For example, the term 3-carboxypropyl-group represents the following substituent:

OH wherein the carboxy group is attached to the third carbon atom of the propyl group, The terms “1-methylpropyl-, “2,2-dimethylpropyl- or “cyclopropylmethyl- group represent the following groups:

CH

The asterisk may be used in sub-formulas to indicate the bond which is connected to the core molécule as defined.

In a définition of a group the term wherein each X, Y and Z group is optionally substituted with and the like dénotés that each group X, each group Y and each group Z either each as a separate group or each as part of a composed group may be substituted as defined. For example a définition R^ex dénotés H, C-|.3-alkyl, Ca-e-cycloalkyl, C3.6-cycloalkyl-Cv3-alkyl or Ci-3-alkyl-O-, wherein each alkyl group is optionally substituted with one or more L^ex. or the like means that in each of the beforementioned groups which comprise the term alkyl, i.e. in each of the groups Ci-3-alkyl, C^-cycloalkyl-Cvralkyl and Ci-₃-alkyl-O-, the alkyl moiety may be substituted with L^ex as defined.

In the following the term bicyclic includes spirocyclic.

Unless specifically indicated, throughout the spécification and the appended claims, a given chemical formula or name shall encompass tautomers and ail stéréo, optical and geometrical isomers (e.g. enantiomers, diastereomers, E/Z \λ/” isomers etc.,.) and racemates thereof as well as mixtures in different proportions of the separate enantiomers, mixtures of diastereomers, or mixtures of any of the foregoing forms where such isomers and enantiomers exist, as well as salts, including pharmaceutically acceptable salts thereof and solvatés thereof such as for instance hydrates including solvatés of the free compounds or solvatés of a sait of the compound.

The phrase pharmaceutically acceptable is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animais without excessive toxicity, irritation, allergie response, or other problem or complication, and commensurate with a reasonable benefit/risk ratio.

As used herein, pharmaceutically acceptable salts refer to dérivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof.

Salts of other acids than those mentioned above which for example are useful for purifying or isolating the compounds of the présent invention (e.g. trifluoro acetate salts) also comprise a part of the invention.

The term halogen generally dénotés fluorine, chlorine, bromine and iodine.

The term “Ci-n-alkyr, wherein n is an integer from 1 to n, either alone or in combination with another radical dénotés an acyclic, saturated, branched or linear hydrocarbon radical with 1 to n C atoms. For example the term Ci-s-alkyl embraces the radicals H3C-, H3C-CH2-, H3C-CH2-CH2-, H₃C-CH(CH3)-, H₃C-CH₂CH₂-CH₂-, HsC-CHz-CHÎCHs)-, H3C-CH(CH₃)-CH₂-, Η₃Ο-Ο(ΟΗ3)2“. h₃c-ch₂-ch₂CH2-CH2-, H₃C-CH2-CH2-CH(CH₃)’, H₃C-CH2-CH(CH3)-CH2-, H₃C-CH(CH₃)-CH₂CH₂-, H3C-CH2-C(CH₃)2-, H₃C-C(CH3)2-CH2-, H₃C-CH(CH₃)-CH(CH₃)- and H₃CCH₂-CH(CH₂CH₃)-. κλζ—

The term Cm-alkylene wherein n is an integer 1 to n, either alone or in combination with another radical, dénotés an acyclic, straight or branched chain divalent alkyl radical containing from 1 to n carbon atoms. For example the term Ci-₄-alkylene includes -(CH₂)-, -(CH₂-CH₂)-, -(CH(CH₃))-, -(CH₂-CH₂-CH₂)-, (C(CH₃)₂)-, -(CH(CH₂CH₃))-, -(CH(CH₃)-CH₂)-, -(CH₂-CH(CH₃))-, -(CH₂-CH₂-CH₂CH₂)-, -(CH₂-CH₂-CH(CH₃))-, -(CH(CH₃)-CH₂-CH₂)-, -(CH₂-CH(CH₃)-CH₂)-, -(CH₂C(CH₃)₂)-, (C (CH₃)2-CH₂)-, -(CH(CH₃)-CH(CH₃))-, -(CH₂-CH(CH₂CH₃))-, (CH(CH₂CH₃)-CH₂)-, -(CH(CH₂CH₂CH₃))-, -(CHCH(CH₃)₂)- and C(CH₃)(CH₂CH₃)-.

The term “C₂._n-alkenyl, is used for a group as defined in the définition for Ci-n-alkyl with at least two carbon atoms, if at least two of those carbon atoms of said group are bonded to each other by a double bond. For example the term C₂.

₃-alkenyl includes -CH=CH₂₁ -CH=CH-CH₃₎ -CH₂-CH=CH₂.

The term C₂-_n-alkenylene is used for a group as defined in the définition for Cvn-alkylene with at least two carbon atoms, if at least two of those carbon atoms of said group are bonded to each other by a double bond. For example the term C₂.₃-alkenylene includes -CH=CH-, -CH=CH-CH₂-, -CH₂-CH=CH-.

The term “C₂._n-alkynyl”, is used for a group as defined in the définition for Ci-n-alkyl with at least two carbon atoms, if at least two of those carbon atoms of said group are bonded to each other by a triple bond. For example the term C₂.₃alkynyl includes -C=CH, -C=C-CH₃, -CH₂-C=CH.

The term C₂-n-alkynylene is used for a group as defined in the définition for Ci-n-alkylene with at least two carbon atoms, if at least two of those carbon atoms of said group are bonded to each other by a triple bond. For example the term C₂.₃-alkynylene includes -C=C-, -C=C-CH₂-, -CH₂-OC-.

The term C₃._n-carbocyclyr as used either alone or in combination with another radical, dénotés a monocyclic, bicyclic or tricyclic, saturated or unsaturated hydrocarbon radical with 3 to n C atoms. The hydrocarbon radical is preferably nonaromatic. Preferably the 3 to n C atoms form one or two rings. In case of a bicyclic or tricyclic ring system the rings may be attached to each other via a single bond or may be fused or may form a spirocyclic or bridged ring system. For example the term C3jo-carbocyclyl includes C₃.io-cylcoalkyl, C3.₁₀-cycloalkenyl, octahydropentalenyl, octahydroindenyl, decahydronaphthyl, indanyl, tetrahydronaphthyl. Most preferably the term C3._n-carbocyclyl dénotés Ο₃._ηcylcoalkyl, in particular C3-7-cycloalkyl.

The term “C₃.n-cycloalkyr, wherein n is an integer 4 to n, either alone or in combination with another radical dénotés a cyclic, saturated, unbranched hydrocarbon radical with 3 to n C atoms. The cyclic group may be mono-, bi-, trior spirocyclic, most preferably monocyclic. Examples of such cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclododecyl, bicyclo[3.2.1.]octyl, spiro[4.5]decyl, norpinyl, norbonyl, norcaryl, adamantyl, etc.

The term “C₃.n-cycloalkenyr', wherein n is an integer 3 to n, either alone or in combination with another radical, dénotés a cyclic, unsaturated but nonaromatic, unbranched hydrocarbon radical with 3 to n C atoms, at least two of which are bonded to each other by a double bond. For example the term C₃.₇-cycloalkenyl includes cyclopropenyl, cyclobutenyi, cyclopentenyl, cyclopentadienyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl, cycloheptadienyl and cycloheptatrienyl.

The term “aryl as used herein, either alone or in combination with another radical, dénotés a carbocyclic aromatic monocyclic group containing 6 carbon atoms which may be further fused to a second 5- or 6-membered carbocyclic group which may be aromatic, saturated or unsaturated. Aryl includes, but is not limited to, phenyl, indanyl, indenyl, naphthyl, anthracenyl, phenanthrenyl, tetrahydronaphthyl and dihydronaphthyl. More preferably the term “aryl as used herein, either alone or in combination with another radical, dénotés phenyl or naphthyl, most preferably phenyl. yS

The term heterocyclyl means a saturated or unsaturated mono-, bi-, tri- or spirocarbocyclic, preferably mono-, bi- or spirocyclic-ring System containing one or more heteroatoms selected from N, O or S(O)_r with r=0, 1 or 2, which in addition may hâve a carbonyl group. More preferably the term heterocyclyl as used herein, either alone or in combination with another radical, means a saturated or unsaturated, even more preferably a saturated mono-, bi- or spirocyclic-ring System containing 1,2, 3 or 4 heteroatoms selected from N, O or S(O)_r with r=0, 1 or 2 which in addition may hâve a carbonyl group, The term “heterocyclyl” is intended to include ail the possible isomeric forms. Examples of such groups include aziridinyl, oxiranyl, azetidinyl, oxetanyl, pyrrolidinyl, tetrahydrofuranyl, piperidinyl, tetrahydropyranyl, azepanyl, piperazinyl, morpholinyl, tetrahydrofuranonyl, tetrahydropyranonyl, pyrrolidinonyl, piperidinonyl, piperazinonyl, morpholinonyl.

Thus, the term heterocyclyl includes the following exemplary structures which are not depicted as radicals as each form may be attached through a covalent bond to any atom so long as appropriate valences are maintained:

E?	D‘	H r— N D	rf'°	0 II □T0
H ô	ô	ô		O II û	°>. z.O O
H	H K	n	H N	H	H N
ô N H	G	o '—N H	C	> Q 5 'b	o s=o II 8
ô '—O	0	û '0	Ô- 0	0 Ô :0 '—s	M ô '—s=o // o \

The term heteroaryl means a mono- or polycyclic, preferably mono- or bicyclicring System containing one or more heteroatoms selected from N, O or S(O)_r with 5 r=0, 1 or 2 wherein at least one of the heteroatoms is part of an aromatic ring, and wherein said ring system may hâve a carbonyl group. More preferably the term heteroaryl as used herein, either alone or in combination with another radical, means a mono- or bicyclic-ring system containing 1, 2, 3 or 4 heteroatoms selected from N, O or S(O)_r with r=0, 1 or 2 wherein at least one of the heteroatoms is part of an aromatic ring, and wherein said ring system may hâve a carbonyl group, The term heteroaryl is intended to include ail the possible isomeric forms.

Thus, the term heteroaryl” includes the following exemplary structures which are not depicted as radicals as each form may be attached through a covalent bond to any atom so long as appropriate valences are maintained:

Many of the terms given above may be used repeatedly in the définition of a formula or group and in each case hâve one of the meanings given above, independently of one another.

Pharmacological Activity

The activity of the compounds of the invention may be demonstrated using the following assay:

The compounds of formula I according to the invention modulate the activity of the G-protein-coupled receptor GPR119. The effect of the compounds on the activation of GPR119 and on the stimulation of intracellular cAMP concentration is determined using the AlphaScreen cAMP Assay Kit (Cat.No.# 6760625R) made by PerkinElmer.

MIN6 cells [Miyazaki J et al. Endocrinology. 1990 Jul; 127(1 ):126-32] are stably transfected with an expression vector for human GPR119 cDNA (Acc. No. NP_848566). Min-6 /hGPR119 cells are cultured in DMEM, 10% FBS, 50μΜ βmercaptoethanol, 0.3mg/mL Geniticin, 2mM GlutaMAX at 37°C 5% CO2. For the assay, the cells are seeded in Optiplates (white, 384-well, 160W- barcoded, TC, stérile with lid, Cat.No.# 6007688 (Perkin Elmer); 10000 cells/well; 50pl). The plates covered with lids are then incubated for 24 hours at 37°C / 5% CO₂. After v the medium is aspirated from the weils completely, 10 pl ofthe test compound are added, the compounds are diluted using stimulating buffer (140mM NaCI, 3.6mM KCI, 0.5mM NaH2PO4, 0.5mM MgSO₄, 1.5mM CaCI₂, 10mM Hepes, 5mM NaHCOa: pH 7,4. 0.5mM IBMX and 0.1% BSA, the final DMSO concentration is 1 %). After 45 minutes incubation at room température (approx. 20°C), the cAMP concentrations are determined using the AlphaScreen cAMP Assay Kit (Cat.No.# 6760625R from PerkinElmer). 10 μΙ of Biotin-cAMP (final concentration 1U/well in lysing buffer (5mM Hepes (pH 7.4), 0.1% BSA, 0.5% Tween) and 10pL Bead solution (final concentration 1 U/well in lysing buffer) are added. The plates are incubated for another 2 hours at room température. The cAMP concentrations are calculated using a cAMP standard curve from the Alpha Screen Counts. The data analysis is carried out by calculating the EC50 value and the maximum value based on a positive control, using suitable software (Graphpad Prism). The compounds according to the invention increase the intracellular cAMP level in the range of 3-5.

The compounds according to the invention typically hâve EC50 values in the range from about 1 nM to about 10 μΜ, preferably from 1 nM to 2 μΜ, preferably less than 1 μΜ, particularly preferably less than 500 nM, most particularly preferably less than 100 nM.

EC50 values for compounds according to the invention are shown in the following Table. The number of the compound corresponds to the number of the Example in the experimental section.

Example	ec50 [nM]	Example	EC50 [nM]	Example	EC50 [nM]	Example	EC50 [nM]
1	21	2	27	3	71	4	52
5	12	6	32	7	35	8	11
9	12	10	152	11	59	12	22
13	28	14	29	15	38	16	17
17	21	18	2	19	25	20	16

Example	EC50 [nM]	Example	EC50 [nM]	Example	EC50 [nM]	Example	EC50 [nM]
21	28	22	6	23	7	24	60
25	62	26	9	27	15	28	22
29	51	30	4	31	3	32	29
33	6	34	18	35	3	36	5
37	6	38	14	39	8	40	2
41	6	42	11	43	9	44	6
45	13	46	18	47	6	48	12
49	25	50	5	51	7	52	19
53	20	55	16	57	36	60	11
61	47	62	20	63	112	64	33
65	228	66	63	67	141	68	60
69	48	70	108	71	16	72	12
73	19	74	52	75	81	76	59
77	19	78	39	79	3	80	5
81	10	82	3	83	3	84	2
85	7	86	12	87	13	88	59
89	16	90	60	91	3	92	10
93	10	94	18

In view of their ability to modulate the activity of the G-protein-coupled receptor GPR119, in particular an agonistic activity, the compounds of general formula (I) according to the invention, including the correspondîng salts thereof, are theoretically suitable for the treatment of ail those diseases or conditions which may be affected or which are mediated by the activation of the G-protein-coupled receptor GPR119,

Accordingly, the présent invention relates to a compound of general formula (I) as a médicament.

Furthermore, the présent invention relates to the use of a compound of general formula (I) or a pharmaceutical composition according to this invention for the treatment and/or prévention of diseases or conditions which are mediated by the activation of the G-protein-coupled receptor GPR119 in a patient, preferably in a human.

In yet another aspect the présent invention relates to a method for treating a disease or condition mediated by the activation of the G-protein-coupled receptor GPR119 in a mammal that includes the step of administering to a patient, preferably a human, in need of such treatment a therapeutïcally effective amount of a compound or a pharmaceutical composition of the présent invention.

Diseases and conditions mediated by agonists of the G-protein-coupled receptor GPR119 embrace metabolic diseases or conditions.

According to one aspect the compounds and pharmaceutical compositions of the présent invention are particularly suitable for treating diabètes mellitus, in particular Type 2 diabètes, Type 1 diabètes, complications of diabètes (such as

e.g. retinopathy, nephropathy or neuropathies, diabetic foot, ulcers or macroangiopathies), metabolic acidosis or ketosis, reactive hypoglycaemia, hyperinsulinaemia, glucose metabolic disorder, insulin résistance, metabolic syndrome, dyslipidaemias of different origins, atherosclerosis and related diseases, obesity, high blood pressure, chronic heart failure, oedema and hyperuricaemia.

The compounds and pharmaceutical compositions of the présent invention are also suitable for preventing beta-cell degeneration such as e.g. apoptosis or necrosis of pancreatic beta cells. The compounds and pharmaceutical compositions of the présent invention are also suitable for improving or restoring the functionality of pancreatic cells, and also for increasing the number and size of pancreatic beta cells. ά/'

Therefore according to another aspect the invention relates to compounds of formula I and pharmaceutical compositions according to the invention for use in preventing, delaying, slowing the progression of and/or treating metabolic diseases, particularly in improving the glycaemic control and/or beta cell function in the patient.

In another aspect the invention relates to compounds of formula I and pharmaceutical compositions according to the invention for use in preventing, delaying, slowing the progression of and/or treating type 2 diabètes, overweight, obesity, complications of diabètes and associated pathological conditions.

In addition the compounds and pharmaceutical compositions according to the invention are suitable for use in one or more of the following therapeutic processes:

- for preventing, delaying, slowing the progression of or treating metabolic diseases, such as for example type 1 diabètes, type 2 diabètes, insufficient glucose tolérance, insulin résistance, hyperglycaemia, hyperlipidaemia, hypercholesterolaemia, dyslipidaemia, syndrome X, metabolic syndrome, obesity, high blood pressure, chronic systemic inflammation, retinopathy, neuropathy, nephropathy, atherosclerosis, endothélial dysfunction or bone-related diseases (such as osteoporosis, rheumatoid arthritis or osteoarthritis);

- for improving glycaemic control and/or reducing fasting plasma glucose, postprandial plasma glucose and/or the glycosylated haemoglobin HbA1c;

- for preventing, delaying, slowing or reversing the progression of disrupted glucose tolérance, insulin résistance and/or metabolic syndrome to type 2 diabètes;

- for preventing, delaying, slowing the progression of or treating a condition or a disease selected from among the complications of diabètes, such as for example retinopathy, nephropathy or neuropathies, diabetic foot, ulcers or macroangiopathies;

- for reducing weight or preventing weight gain or assisting weight loss; vv

- for preventing or treating the dégradation of pancreatic beta cells and/or improving and/or restoring the functionality of pancreatic beta cells and/or restoring the functionality of pancreatic insulin sécrétion;

- for maintaining and/or improving insulin sensitivity and/or preventing or treating hyperinsulinaemia and/or insulin résistance.

In particular, the compounds and pharmaceutical compositions according to the invention are suitable for the treatment of obesity, diabètes (comprising type 1 and type 2 diabètes, preferably type 2 diabètes mellitus) and/or complications of diabètes (such as for example retinopathy, nephropathy or neuropathies, diabetic foot, ulcers or macroangiopathies).

The compounds according to the invention are most particularly suitable for treating type 2 diabètes mellitus.

The dose range ofthe compounds of general formula (I) applicable perday is usually from 0.001 to 10 mg per kg body weight, for example from 0.01 to 8 mg per kg body weight ofthe patient. Each dosage unit may conveniently contain from 0.1 to 1000 mg, for example 0.5 to 500 mg.

The actual therapeutically effective amount or therapeutic dosage will of course dépend on factors known by those skilled in the art such as âge and weight of the patient, route of administration and severity of disease. In any case the compound or composition will be administered at dosages and in a manner which allows a therapeutically effective amount to be delivered based upon patient’s unique condition.

The compounds, compositions, including any combinations with one or more additional therapeutic agents, according to the invention may be administered by oral, transdermal, inhalative, parentéral or sublingual route. Ofthe possible methods of administration, oral or intravenous administration is preferred.

Pharmaceutical Compositions

Suitable préparations for administering the compounds of formula (I), optionally in combination with one or more further therapeutic agents, will be apparent to those with ordinary skill in the art and include for example tablets, pills, capsules, suppositories, lozenges, troches, solutions, syrups, élixirs, sachets, injectables, inhalatives and powders etc. Oral formulations, partîcularly solid forms such as

e.g. tablets or capsules are preferred. The content of the pharmaceutically active compound(s) is advantageously in the range from 0.1 to 90 wt.-%, for example from 1 to 70 wt.-% of the composition as a whole.

Suitable tablets may be obtained, for example, by mixing one or more compounds according to formula (I) with known excipients, for example inert diluents, carriers, disintegrants, adjuvants, surfactants, binders and/or lubricants. The tablets may also consist of several layers. The particular excipients, carriers and/or diluents that are suitable for the desired préparations will be familiar to the skilled man on the basis of his speciaiist knowledge. The preferred ones are those that are suitable for the particular formulation and method of administration that are desired. The préparations or formulations according to the invention may be prepared using methods known per se that are familiar to the skilled man, such as for example by mixing or combining at least one compound of formula I according to the invention, or a pharmaceutically acceptable sait of such a compound, and one or more excipients, carriers and/or diluents.

Combination Therapy

The compounds of the invention may further be combined with one or more, preferabiy one additional therapeutic agent According to one embodiment the additional therapeutic agent is selected from the group of therapeutic agents useful in the treatment of diseases or conditions described hereinbefore, in particular associated with metabolic diseases or conditions such as for example diabètes mellitus, obesity, diabetic complications, hypertension, hyperlipidemia. Additional therapeutic agents which are suitable for such combinations include in particular those which for example potentiate the therapeutic effect of one or more active substances with respect to one of the indications mentîoned and/or which allow the dosage of one or more active substances to be reduced.

Therefore a compound of the invention may be combined with one or more additional therapeutic agents selected from the group consisting of antidiabetic agents, agents for the treatment of overweigth and/or obesity and agents for the treatment of high blood pressure, heart failure and/or atherosclerosis.

Antidiabetic agents are for example metformin, sulphonylureas, nateglinide, repaglinide, thiazolidinediones, PPAR-(alpha, gamma or alpha/gamma) agonists or modulators, alpha-glucosidase inhibitors, DPPIV inhibitors, SGLT2-inhibitors, insulin and insulin analogues, GLP-1 and GLP-1 analogues or amylin and amylin analogues, cycloset, 11 β-HSD inhibitors. Other suitable combination partners are inhibitors of protein tyrosinephosphatase 1, substances that affect deregulated glucose production in the liver, such as e.g. inhibitors of glucose-6-phosphatase, or fructose-1,6-bisphosphatase, glycogen phosphorylase, glucagon receptor antagonists and inhibitors of phosphoenol pyruvate carboxykinase, glycogen synthase kinase or pyruvate dehydrokinase, alpha2-antagonists, CCR-2 antagonists or glucokinase activators. One or more lipid Iowering agents are also suitable as combination partners, such as for example HMG-CoA-reductase inhibitors, fibrates, nicotinic acid and the dérivatives thereof, PPAR-(alpha, gamma or alpha/gamma) agonists or modulators, PPAR-delta agonists, ACAT inhibitors or cholestérol absorption inhibitors such as, bile acid-binding substances such as, inhibitors of ileac bile acid transport, MTP inhibitors, or HDL-raising compounds such as CETP inhibitors or ABC1 regulators.

Therapeutic agents for the treatment of overweight and/or obesity are for example antagonists ofthe cannabinoidl receptor, MCH-1 receptor antagonists, MC4 receptor agonists, NPY5 or NPY2 antagonists, β 3-agonists, leptin or leptin mimetics, agonists of the 5HT2c receptor.

Therapeutic agents for the treatment of high blood pressure, chronic heart failure and/or atherosclerosis are for example A-ll antagonists or ACE inhibitors, ECE inhibitors, diuretics, β-blockers, Ca-antagonists, centrally acting antihypertensives, antagonists of the alpha-2-adrenergic receptor, inhibitors of neutral endopeptidase, thrombocyte aggregation inhibitors and others or combinations thereof are suitable. Angiotensin II receptor antagonists are preferably used for the treatment or prévention of high blood pressure and complications of diabètes, often combined with a diuretic such as hydrochiorothiazide.

The dosage for the combination partners mentioned above is usually 1/5 of the lowest dose normally recommended up to 1/1 of the normally recommended dose.

Preferably, compounds of the présent invention and/or pharmaceutical compositions comprising a compound of the présent invention optionally in combination with one or more additional therapeutic agents are administered in conjunction with exercise and/or a diet.

Therefore, in another aspect, this invention relates to the use of a compound according to the invention in combination with one or more additional therapeutic agents described hereinbefore and hereinafter for the treatment of diseases or conditions which may be affected or which are mediated by the activation of the G-protein-coupled receptor GPR119, in particular diseases or conditions as described hereinbefore and hereinafter.

In yet another aspect the présent invention relates a method for treating a disease or condition mediated by the activation of the G-protein-coupled receptor GPR119 in a patient that includes the step of administering to the patient, preferably a human, in need of such treatment a therapeutically effective amount of a compound of the présent invention in combination with a therapeutically effective amount of one or more additional therapeutic agents described in hereinbefore and hereinafter,

The use of the compound according to the invention in combination with the additional therapeutic agent may take place simultaneously or at staggered times.

The compound according to the invention and the one or more additional therapeutic agents may both be présent together in one formulation, for example a tablet or capsule, or separately in two identical or different formulations, for example as a so-called kit-of-parts.

Consequently, in another aspect, this invention relates to a pharmaceutical composition which comprises a compound according to the invention and one or more additional therapeutic agents described hereinbefore and hereinafter, optionally together with one or more inert carriers and/or diluents.

Other features and advantages of the présent invention will become apparent from the following more detailed Examples which illustrate, by way of example, the principles of the invention.

Examples

The terms ambient température and room température are used interchangeably and designate a température of about 20 ^eC.

Preliminarv remarks:

As a rule, ¹H-NMR and/or mass spectra hâve been obtained for the compounds prepared. The R_f values are determined using Merck silica gel 60 F254 plates and UV light at 254 nm.

Compounds given with a spécifie configuration at a stereocenter are isolated as pure isomers. The configuration of the stereocenter is arbitrarily assigned. Any compound following a compound with an arbitrarily assigned configuration is given the analogous configuration.

Analytical HPLC parameters employed for characterization of products (TFA dénotés trifluoroacetic acid):

method 1

Waters XBridge C18, 4.6 x

method 2

Waters XBridge C18,

column	30 mm, 3.5 pm	column	4.6 x 30 mm, 3.5 pm
mobile phase	A: water+ 0.1% TFA B: methanol + 0.1% TFA	mobile phase	A: water + 0.1 % TFA B: methanol
TIME (min)	A%	B%	TIME (min)	A%	B%
0.0	95	5	0.0	95	5
0.20	95	5	1.6	0	100
1.5	0	100	1.85	0	100
1.75	0	100	1.9	95	5
1.85	95	5
flow rate	4.0 mL/min	flow rate	4.8 mL/min
wavelength	UV 220, 230, or 254 nm	wavelength	UV 220, 230, or 254 nm

method 3 column	Waters XBridge C18, 4.6 x 30 mm, 3.5 pm	method 4	Waters XBridge C18, 3 x 30 mm, 2.5 pm
mobile phase	A: water + 0.1% TFA B: methanol + 0.1% TFA		A: water + 0.1 % TFA B: methanol
TIME (min)	A%	B%	TIME (min)	A%	B%
0.0	95	5	0.0	95	5
0.20	95	5	0.05	95	5
1.5	0	100	1.40	0	100
1.9	0	100	1.80	0	100
2.0	95	5
flow rate	4.0 mL/min	flow rate	2.2 mL/min
wavelength	UV 220, 230, or 254 nm	wavelength	UV 220, 230, or 254 nm

method 5 column	Waters XBridge C18, 4.6 x 30 mm, 3.5 pm	method 6 column	Waters XBridge C18, 4,6 x 30 mm, 3.5 pm
mobile phase	A: water+ 0.1% TFA B: methanol	mobile phase	A: water+ 0.1% HCOOH B: methanol
	TIME (min)	A%	B%		TIME (min)	A%	B%
	0.0	95	5		0.0	95	5
	1.6	0	100		1.15	95	5
	1.85	0	100		1.7	0	100
	1.9	95	5		2.25	0	100
flow rate	4.0 mL/min	flow rate	4.0 mL/min
wavelength	UV 220, 230, or 254 nm	wavelength	UV 220, 230, or 254 nm

method 7 column	Waters XBridge C18, 3 x 30 mm, 2.5 pm	method 8 column	Waters Sunfire C18, 3 x 30 mm, 2.5 pm
mobile phase	A: water + 0.1% NH4OH B: methanol	mobile phase	A: water+ 0.1% TFA B: methanol
TIME (min)	A%	B%	TIME (min)	A%	B%
0.0	95	5	0,00	95	5
0.05	95	5	1.25	95	5
1.40	0	100	1.70	0	100
1.80	0	100	1.75	0	100
			1.90	0	100
flow rate	2.2 mL/min	flow rate	1.8 mL/min
wavelength	UV 220, 230, or 254 nm | wavelength	UV 220, 230, or 254 nm

method 9 column	Waters Sunfire C18, 4.6 x 50 mm, 3.5 pm	method 10 column	Waters Sunfire C18, 4.6 x 30 mm, 3.5 pm, 60 °C
mobile phase	A: water + 0.1 % TFA B: methanol	mobile phase	A: water + 0.1% HCOOH B: methanol
TIME (min)	A%	B%	TIME (min)	A%	B%
0.00	80	20	0.00	95	5
1.70	0	100	0.15	95	5
2.50	0	100	1.70	0	100
2.60	80	20	2.25	0	100
flow rate	2.0 mL/min	flow rate	4.0 mL/min
wavelength	DAD 210-500 nm	wavelength	DAD 210-500 nm

Intermediate 1

-(4-Benzofuran-2-yl-piperidin-1 -yl)-2,2,2-trifluoro-ethanone

Trifluoroacetic anhydride (9.41 mL) is added dropwise to a mixture of 4benzofuran-2-yl-piperidine hydrochloride (8.00 g) and triethylamine (14.19 mL) in 10 dichloromethane (80 mL) at 0 °C. The resulting mixture is warmed to room température, washed with water and aqueous NaHCO₃ solution, dried (MgSO₄), and the solvent is evaporated. The crude product is used without further purification. LC (method 3): tR = 1.39 min; Mass spectrum (ESI⁺): m/z = 298 [M+H]⁺.

Intermediate 2

1-r4-(2,3-Dihvdro-benzofuran-2-vl)-piperidin-1-vl1-2,2,2-trifluoro-ethanone

A mixture of 1-(4-benzofuran-2-yl-piperidin-1-yl)-2_l2,2-trifluoro-ethanone (11.50 g),

10% palladium on carbon (1.15 g), ethyl acetate (135 mL) and methanol (15 mL) is shaken under hydrogen atmosphère (3.5 bar) at room température for 24 h.

The catalyst is then separated by filtration and the filtrate is concentrated to give an oil that is submitted to the next reaction without further purification. LC (method

2): t_R = 1.34 min.

Intermediate 3

1-f4-(5-Bromo-2,3-dihvdro-benzofuran-2-yi)-piperidÎn-1-vll-2,2,2-trifluoro-ethanone

F

The title compound is prepared from 1-[4-(2,3-dihydro-benzofuran-2-yl)-piperidin-

1-yl]-2,2,2-trifluoro-ethanone and N-bromo-succinimide following a procedure analogous to that described for Intermediate 1. LC (method 2): t_R = 1.47 min; Mass spectrum (ESl·): m/z = 378 [M+H]⁺.

Intermediate 4

4-[5-(4-Methanesulfonvl-phenvl)-2,3-dihydro-benzofuran-2-vll-piperidine

To a mixture of 1-[4-(5-bromo-2,3-dihydro-benzofuran-2-yl)-piperidin-1-yl]-2,2,2trifluoro-ethanone (2.50 g) and 4-(methanesulfonyl)phenyl boronic acid (1.45 g) in Ν,Ν-dimethylformamide (25 mL) a 2 M aqueous Na₂CO₃ solution (8.26 mL) is added. The mixture is sparged with argon for 10 min and PdCI₂[1,rbis(diphenylphosphino)-ferrocene]-CH₂CI₂ complex (540 mg) is added, The resulting mixture is stirred over night at 90 °C. After cooling to room température, water (50 mL) and ethyl acetate (100 mL) are added and the aqueous phase is v extracted with ethyl acetate. The organic phase is washed with water and brine, dried (MgSO₄), and the solvent is evaporated. The residue is chromatographed on silica gel [dichloromethane/ (methanol/NH₄OH 9:1 ) 90:10 - 80:20] to give the title compound, since the trifluoroacetyl group is removed under the reaction conditions. LC (method 1): t_R = 0.88 min; Mass spectrum (ESI⁺): m/z = 358 [M+H]⁺.

Intermediate 5

4-r5-(4-Methanesulfonvl-phenvD-2,3-dihydro-benzofuran-2-vl]-piperidine-1carbonitrile o

.0

Ethyldiisopropylamine (0.96 mL) and bromonitirile (175 mg) are added to a solution of 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydro-benzofuran-2-yl]piperidine (400 mg) in dichloromethane (10 mL) and tetrahydrofuran (10 mL), and the reaction mixture is stirred over night at room température. Dichloromethane and water are added and the organic phase is separated and washed with water, 10% NH4CI solution, and brine, and dried over MgSC>4. The solvent is evaporated and the residue is triturated with diethyl ether to give a brownish solid. Since this material still contains ethyldiisopropylamine hydrochloride, ethyl acetate and water are added. The organic phase is separated, dried over MgSO₄ and concentrated in vacuo. The residue is again triturated with diethyl ether to afford the title compound. LC (method 2): t_R = 1.18 min; Mass spectrum (ESI⁺): m/z = 383 [M+H]⁺.

Intermediate 6

4-(5-Chloro-furor2.3-clpvridin-2-vl)-piperidine-1-carboxylic acid tert-butyl ester

Copper(l) iodide (25 mg) and bis-(triphenylphosphin)-palladium(ll)-chloride (30 mg) are added to 6-chloro-4-iodo-pyridin-3-ol (200 mg) in N,N-dimethylformamide (3 mL) under an argon atmosphère. Triethylamine (110 pL) is added and the resulting mixture is stirred at room température for 1 h. A solution of 4-ethynylpiperidine-1-carboxylic acid tert-butyl ester (175 mg) in Ν,Ν-dimethylformamide (2 mL) is added dropwise and the reaction mixture is stirred at 55°C for 3 h. The solvent is evaporated and the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 70:30) to give the title compound. LC (method 2): t_R = 1.40 min; Mass spectrum (ESI⁺): m/z = 337 [M+H]⁺.

Intermediate 7

4-[5-(4-Methanesulfonvl-phenvl)-furof2,3-c1pvridin-2-vl1-piperidine-1-carboxvlic acid tert-butyl ester .0

A mixture of 4-(5-chloro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tertbutyl ester (390 mg), 4-(methanesulfonyl)phenyl boronic acid (350 mg), aqueous Na2CO₃ solution (2 M; 1.50 mL), and dioxane (10 mL) is sparged with argon for 10 min and Pd(PPh3)4 (100 mg) is added. The resulting mixture is heated to 170 °C in a microwave oven until the conversion is complété. The reaction mixture is concentrated in vacuo, diluted with water and extracted with ethyl acetate. The organic phase is washed with brine, dried over MgSO₄, and the solvent is evaporated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 60:40 —► 40:60) to give the title compound. LC (method 5): t_R = 1.32 min; Mass spectrum (EST): m/z = 457 [M+H]⁺.

Intermediate 8

4-|'5-(4-MethanesulfonylPhenyl)-2.3-dihvdro-furo[2,3-clpyridin-2-vl1-piperidine-1carboxylic acid tert-butyl ester

A mixture of 4-[5-(4-methanesulfonyl-phenyl)-furo[2_l3-c]pyridin-2-yl]-piperidine-1carboxylic acid tert-butyl ester (155 mg), acetic acid (4.0 mL) and 10% palladium on carbon (40 mg) in methanol (10 mL) is shaken under an hydrogen atmosphère (5 bar) at 50°C. The catalyst is filtered off and the filtrate is concentrated in vacuo to give the title compound. LC (method 5): îr = 1.32 min; Mass spectrum (ESI*): m/z = 459 [M+H]*,

Intermediate 9

5-(4-Methanesulfonvl-phenvl)-2-piperidin-4-vl-2,3-dihydro-furo[2,3-clpvridine

A mixture of 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]piperidine-1-carboxylic acid tert-butyl ester (190 mg) and trifluoro acetic acid (0.40 mL) in dichloromethane (3 mL) is stirred at room température for 2 h. The reaction mixture is diluted with dichloromethane and washed with aqueous Na2CO₃ solution. The aqueous phase is extracted dichloromethane and the combined organic phases are washed with water, dried over MgSO₄, and concentrated in vacuo. LC (method 5): t_R = 0.62 min; Mass spectrum (ESI*): m/z = 359 [M+H]*.

Intermediate 10

4-r5-(4-Methanesulfonvl-phenvl)-2.3-dihydro-furor2,3-c]pvridin-2-vl1-piperidine-1carbonitrile

The title compound is prepared from 5-(4-methanesulfonyl-phenyi)-2-piperidin-4yl-2,3-dihydro-furo[2,3-c]pyridine and bromonitirile foilowing a procedure analogous to that described for Intermediate 5. LC (method 5): îr = 0.91 min; Mass spectrum (ESl·): m/z = 384 [M+H]⁺.

Intermediate 11

N-Hvdroxv-4-[5-(4-methanesulfonvl-phenyl)-2,3-dihydro-furoF2,3-clpvridin-2-vllpiperidine-1 -carboxamidine

A mixture of 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]piperidine-1-carbonitrile (175 mg), hydroxylamine hydrochloride (50 mg), potassium carbonate (70 mg), éthanol (1 mL), and water (1.5 mL) is heated under reflux for 2h.

The reaction mixture is concentrated in vacuo and chromatographed on silica gel (dichloromethane/methanol 92:8 -> 60:40) to give the title compound. LC (method

5): tR = 0.65 min; Mass spectrum (EST): m/z = 417 [M+H]⁺.

Intermediate 12

4-[2-(5-Bromo-2-chloro-pyridin-4-vl)-acetyll-piperidine-1 -carboxylic acid tert-butyl ester

Lithium bis(trimethylsilyl)amide solution (1.0 M in tetrahydrofuran; 11.00 mL) is added drop wise to 5-bromo-2-chloro-4-picoline (950 mg) in tetrahydrofuran (15 mL) at -40°C under an argon atmosphère. The mixture is stirred for 2 h at -35°C to -45°C prior to the addition of piperidine-1,4-dicarboxylic acid 1 -tert-butyl ester 4ethyl ester (1.33 g), dissolved in tetrahydrofuran (15 mL). The reaction mixture is allowed to warm to room température over a period of 1 h. Ice cold water is added and the mixture is extracted with ethyl acetate. The combined extracts are washed with brine,_dried over MgSO₄, and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 75:25 -> 60:40) to give the title compound. LC (method 5): tp = 1.43 min; Mass spectrum (ESI⁺): m/z = 417, 419 [M+H]⁺.

Intermediate 13

4-r2-(5-Bromo-2-chloro-pvridin-4-vl)-1-hvdroxv-ethvll-piperidine-1-carboxvlic acid tert-butyl ester

Sodium borohydride (240 mg) is added to an ice-cooled solution of 4-[2-(5-bromo-

2-chloro-pyridin-4-yl)-acetyl]-piperidine-1 -carboxylic acid tert-butyl ester (1.65 g) in a mixture of tetrahydrofuran (40 mL) and water (10 mL). The resulting mixture stirred for 0.5 h. 2 N Citric acid is added and the mixture is extracted with ethyl acetate. The combined extracts are washed with aqueous NaHCO₃ solution and brine, dried over MgSO₄, and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 65:35) to give the title compound. LC (method 5): t_R = 1.48 min; Mass spectrum (ESI⁺): m/z = 419, 421 [M+H]⁺.

Intermediate 14

4-(5-Chloro-2,3-dihvdro-furor2,3-clpvridin-2-yl)-piperidine-1-carboxvlic acid tertbutyl ester

A mixture of 4-[2-(5-bromo-2-chloro-pyridin-4-yl)-1-hydroxy-ethyl]-piperidine-1carboxylic acid tert-butyl ester (11.60 g), palladium acetate (500 mg), racemic 2(di-tert-butylphosphino)-1,T-binapthyl (1.00 g), and césium carbonate (14.00 g) in toluene (150 mL) is heated in an oil bath at 110°C under an argon atmosphère for

h. After cooling to room température ethyl acetate and water are added and the organic phase is separated, washed with brine, dried over MgSO₄, and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyi acetate 70:30 -» 50:50) to give the title compound. LC (method 5): îr = 1.44 min; Mass spectrum (ESI⁺): m/z = 339 [M+H]⁺.

Intermediate 15

4-[5-(4-Methanesulfonvlmethvl-phenvl)-2,3-dihydro-furo[2,3-clpyridin-2-vllpiperidine-1-carboxylic acid tert-butyl ester

O

The title compound is prepared from 4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2yl)-piperidine-1 -carboxylic acid tert-butyl ester and [4[(methylsulfonyl)methyl]phenyl] boronic acid following a procedure analogous to that described for Intermediate 7. LC (method 6): tR = 1.54 min; Mass spectrum (ESI⁺): m/z = 473 [M+H]⁺.

Intermediate 16

5-(4-Methanesulfonvlmethvl-phenvl)-2-piperidin-4-vl-2,3-dihvdro-furof2,3clpyridine

HN

The title compound is prepared from 4-[5-(4-methanesulfonylmethyl-phenyl)-2,3dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carboxylic acid tert-butyl ester following a procedure analogous to that described for Intermediate 9. LC (method

6): Ir = 0.73 min; Mass spectrum (ESI⁺): m/z = 373 [M+H]⁺.

Intermediate 17

4-(5-(4-Methanesulfonylrr)ethyl-phenyl)-2,3-dihydro-furof2,3-clpyridin-2-yllpiperidine-1-carbonitrile

The title compound is prepared from 5-(4-methanesulfonylmethyl-phenyl)-2piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method 6): tp = 1.11 min; Mass spectrum (EST): m/z = 398 [M+H]⁺.

Intermediate 18

N-Hvdroxv-4-r5-(4-methanesulfonvlmethvl-phenYl)-2,3-dihvdro-furo[2,3-clpyridin-

2-vl]-piperidine-1-carboxamidine

The title compound is prepared from 4-[5-(4-methanesulfonylmethyl-phenyl)-2,3dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carbonitrile and hydroxylamine hydrochloride following a procedure analogous to that described for Intermediate

11. LC (method 5): tR = 0.83 min; Mass spectrum (ESI⁺): m/z = 431[M+H]⁺.

Intermediate 19

4-r5-(1Methanesulfonvl-1,2,3,6-tetrahydro-pyridin-4-vl)-2.3-dihydro-furor2,3clpyridin-2-yl1-piperidine-1-carboxvlic acid tert-butyl ester

The title compound is prepared from 4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2yl)-piperidine-1-carboxylic acid tert-butyl ester and 1-(methylsulfonyl)-4-(4,4,5,5tetramethyl-ί ,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine following a procedure analogous to that described for Intermediate 7. LC (method 5): îr =

1.12 min; Mass spectrum (ESI⁺): m/z = 464 [M+H]⁺.

Intermediate 20

5-( 1 -Methanesulfonvl-1.2.3,6-tetrahydro-pvridin-4-yl)-2-piperidin-4-vl-2,3-dihvdro- furo[2,3-clpyridine

The title compound is prepared from 4-[5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tertbutyl ester following a procedure analogous to that described for Intermediate 9. LC (method 5): îr = 0.44 min; Mass spectrum (ESI⁺): m/z = 364 [M+H]⁺.

Intermediate 21

4-f5-(1-Methanesulfonvl-1,2,3,6-tetrahydro-pvridin-4-vl)-2,3-dihydro-furoF2,3c]pvridine-2-vl1-piperidine-1-carbonitrile

o

The title compound is prepared from 5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method

5): t_R = 0.70 min; Mass spectrum (ESI⁺): m/z = 389 [M+Hf,

Intermediate 22

4“Γ5-(2-Fluoro-4-methanesulfonylmethvl·phenvl¾-2.3-dihγdro-furoΓ2,3-clpvridin-2yl]-piperidine-1-carboxvlic acid tert-butyl ester

The title compound is prepared from 4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-2yl)-piperidine-1-carboxylic acid tert-butyl ester and 2-(2-fluoro-4methanesulfonylmethyl-phenyl)-4,4.5,5-tetramethyl-[1,3,2]dioxaborolane following a procedure analogous to that described for Intermediate 7. LC (method 6): tR = 1.61 min; Mass spectrum (EST): m/z = 491 [M+H]⁺.

Intermediate 23

5-(2-Fluoro-4-methanesulfonvlmethvl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3clpyridine

The title compound is prepared from 4-[5-(2-fluoro-4-methanesulfonylmethylphenyO^.S-dihydro-furo^.S-clpyridin^-ylJ-piperidine-l-carboxylic acid tert-butyl ester following a procedure analogous to that described for Intermediate 9. LC (method 6): t_R = 0.78 min; Mass spectrum (EST): m/z = 391 [M+H]⁺.

Intermediate 24

4-[5-(2-Fluoro-4-methanesulfonvlmethvl-phenvl)-2,3-dihvdro-furo[2,3-clpvridin-2vll-piperidine-1 -carbonitrile

The title compound is prepared from 5-(2-fluoro-4-methanesulfonylmethyl-phenyl)-

2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method 6): t_R = 1.21 min; Mass spectrum (ESl·): m/z = 416 [M+H]⁺.

Intermediate 25

N-Hvdroxv-4-[5-(1-methanesulfonvl-1,2,3,6-tetrahvdro-pvridin-4-vl)-2,3-dihydro- furof2,3-c1pyridin-2-vn-piperidine-1-carboxamidine

The title compound is prepared from 4-(5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2_T3-dihydro-furo[2,3-c]pyridine-2-yl]-piperidine-1-carbonitrile and hydroxylamine hydrochloride following a procedure analogous to that described for Intermediate 11. LC (method 5): tR = 0.54 min; Mass spectrum (ESI⁺): m/z = 422 [M+H]⁺.

Intermediate 26

4-r5-(2-Fluoro-4-methanesulfonylmethyl-phenyl)-2,3-dihydro-furo[2,3-clpyridin-2yll-N-hydroxy-piperidine-1-carboxamidine

The title compound is prepared from 4-[5-(2-fluoro-4-methanesulfonylmethylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile and hydroxylamine hydrochloride following a procedure analogous to that described for Intermediate 11. LC (method 6): Ir = 0.90 min; Mass spectrum (ESI⁺): m/z = 449 [M+H]⁺.

Intermediate 27

4-[2-(5-Bromo-2-chloro-pyridin-4-yl)-1-hvdroxy-1-methvl-ethvll-piperidine-1carboxylic acid tert-butyl ester

A solution of 4-[2-(5-bromo-2-chloro-pyridin-4-yl)-acetyl]-piperidine-1-carboxylic acid tert-butyl ester (9.80 g) in tetrahydrofuran (6 mL) is added drop wise to an ice cooled solution of methyl magnésium bromide (1.4 M in toluene/tetrahydrofuran 75:25,74 mL). The reaction mixture is stirred for 30 min, warmed to room température and stirred for 1 h. The mixture is poured onto aqueous NH4CI solution and extracted with ethyl acetate. The combined extracts are dried over MgSO4 and concentrated in vacuo. Toluene is added to the residue and evaporated several times. Since the residue still contains a considérable amount of starting material, it is again treated with the Grignard reagent following the procedure described above. The crude product is purified by préparative HPLC (column: Waters Χ-Bridge C18; mobile phase: water+0.125 % NH₄OH/methanol 90:10 100:0) to give the title compound. LC (method 4): t_R = 1.33 min; Mass spectrum (ESI*): m/z = 433, 435 [M+H]⁺.

Intermediate 28

4-(5-Chloro-2-methvl-2,3-dihvdro-furo[2,3-clpvridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester ci

The title compound is prepared from 4-[2-(5-bromo-2-chloro-pyridin-4-yl)-1hydroxy-1-methyl-ethyl]-piperidine-1 -carboxylic acid tert-butyl ester following a procedure analogous to that described for Intermediate 14. LC (method 4): t_R = 1.29 min; Mass spectrum (ESI*): m/z = 353 [M+H]⁺.

Intermediate 29 and 30 (S)-4-(5-Chloro-2-methvl-2.3-dihvdro-furo[2,3-clpvridin-2-yl)-piperidine-1carboxylic acid tert-butyl ester and (/?)-4-(5-Chloro-2-methyl-2,3-dihvdro-furof2,3clpyridin-2-vl)-piperidine-1-carboxylic acid tert-butyl ester

Ci

Cl

The title compounds are obtained in separate fractions upon SFC on chiral phase of racemic Intermediate 28 (column: Daicel IC, 250x20 mm; mobile phase: methanol containing 0.2% diethylamine/sc carbon dioxide 25:75; flow rate 60 ml/min). The configuration of the stereocenter is arbitrarily assigned; rétention times on the SFC on chiral phase (Daicel IC, 250x4.6 mm; mobile phase: methanol containing 0.2% diethylamine/sc carbon dioxide 25:75; flow rate 4 ml/min): Intermediate 29: t_R = 3.77 min; Intermediate 30; tR = 4.42 min.

Intermediate 31 (SMf5-(4-Methanesulfonvl-phenvl)-2-methvl-2,3-dihvdro-furor2,3-clpyridin-2-vl1-

The title compound is prepared from (S)-4-(5-chloro-2-methyl-2,3-dihydro-furo[2,3c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 29; the configuration of the stereocenter is arbitrarily assigned) and 4(methanesulfonyl)phenylboronic acid following a procedure analogous to that described for Intermediate 7. LC (method 4): t_R = 1.19 min; Mass spectrum (ESI⁺): m/z = 473 [M+H]⁺.

Intermediate 32 (S)-5-(4-Methanesulfonvl-phenvl)-2-methvl-2-piperidin-4-vl-2₁3-dihvdro-furo[2₁3“ clpyridine

The title compound is prepared from (S)-4-[5-(4-methanesulfonyl-phenyl)-2methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carboxylic acid tert-butyl ester (Intermediate 31 ; the configuration of the stereocenter is arbitrarily assigned) following a procedure analogous to that described for Intermediate 9. LC (method

7): îr = 0.63 min; Mass spectrum (ESI⁺): m/z = 373 [M+H]⁺.

Intermediate 33 (S)-4-f5-(4-Methanesulfonyl-phenvl)-2-methyl-2,3-dihvdro-furor2,3-clDvridin-2-vllpiperidine-1 -carbonitrite

The title compound is prepared from (S)-5-(4-methanesulfonyl-phenyl)-2-methyl-2piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 32; the configuration of the stereocenter is arbitrarily assigned) and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method 4): t_R = 0.87 min; Mass spectrum (ESI⁺): m/z = 398 [M+H]⁺,

Intermediate 34 and 35 (F?)-4-(5-Chloro-2.3-dihvdro-furof2,3-clpyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and (S)-4-(5-Chloro-2,3-dihydro-furor2,3-clDvridin-2-vl)-piperidine-

1-carboxylic acid tert-butyl ester

The title compounds are obtained in separate fractions upon SFC on chiral phase of racemic Intermediate 14 (column: Daîcel IC, 250x20 mm; mobile phase: éthanol containing 0.2% diethylamine/sc carbon dioxide 25:75; flow rate 50 ml/min). The configuration of the stereocenter is arbitrarily assigned; rétention times on the SFC on chiral phase (Daicel IC, 250x4.6 mm; mobile phase: éthanol containing 0.2% diethylamine/sc carbon dioxide 25:75; flow rate 4 ml/min): Intermediate 34: t_R = 1.64 min; Intermediate 35; t_R = 1.91 min.

Intermediate 36 (S)-4-[5-(1-Methanesulfonyl-1,2,3,6-tetrahvdro-Dvridin-4-vl)-2,3-dihydro-furo[2,3clDvridin-2-vn-piperidine-1-carboxylic acid tert-butyl ester

The title compound is prepared from (S)-4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-

2-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 35, the configuration ofthe stereocenter is arbitrarily assigned) and 1-(methylsulfonyl)-4(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine following a procedure analogous to that described for Intermediate 7. LC (method 5): îr = 1.10 min; Mass spectrum (EST): m/z = 464 [M+H]⁺.

Intermediate 37 (S)-5-(1-Methanesulfonvl-1,2,3,6-tetrahvdro-pyridin-4-vl)-2-piperidin-4-vl-2,3dihvdro-furo(2,3-c1pyridine

The title compound is prepared from (S)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydrO“furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 36, the configuration ofthe stereocenter is arbitrarily assigned) following a procedure analogous to that described for Intermediate 9. LC (method 5): t_R = 0.44 min; Mass spectrum (EST): m/z = 364 [M+H]⁺.

Intermediate 38 (/?)-4-[5-(1-Methanesulfonyl-1,2,3,6-tetrahvdro-pvridin-4-vl)-2.3-dihvdro-furo[2,3c1pvridin-2-yl1-piperidine-1-carboxylic acid tert-butyl ester —

The title compound is prepared from (/?)-4-(5-chloro-2,3-dihydro-furo[2,3-c]pyridin-

2-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 34, the configuration of the stereocenter is arbitrarily assigned) and 1-(methylsulfonyl)-4(4,4,5_l5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine foliowing a procedure analogous to that described for Intermediate 7. LC (method 5): îr = 1.10 min; Mass spectrum (ESI⁺): m/z = 464 [M+H]⁺.

Intermediate 39 (/3)-5-( 1-Methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-piperidin-4-yl-2,3dihvdro-furo[2,3-c1pyridine

The title compound is prepared from (R)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 38, the configuration of the stereocenter is arbitrarily assigned) foliowing a procedure analogous to that described for Intermediate 9. LC (method 5): îr = 0.44 min; Mass spectrum (ESI⁺): m/z = 364 [M+H]⁺.

Intermediate 40 (S)-4-[5-(1-Methanesulfonvl-1,2,3,6-tetrahvdro-pvridin-4-vl)-2-methyl-2,3-dihydrofuror2.3-clpvridin-2-yl1-piperidine-1-carboxvlic acid tert-butyl ester \k/—

The title compound is prepared from (S)-4-(5-chloro-2-methyl-2,3-dihydro-furo[2,3c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 29; the configuration ofthe stereocenter is arbitrarily assigned) and 1-(methylsulfonyl)-4(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine following a procedure analogous to that described for Intermediate 7. LC (method 4): îr = 1.02 min; Mass spectrum (ESI⁺): m/z = 478 [M+Hf.

Intermediate 41 (S)-5-(1-Methanesulfonvl-1.2.3,6-tetrahvdro-pyridin-4-yl)-2-methyl-2-piperidin-4-yl-

2,3-dihvdro-furo[2,3-c1pyridine

HN

The title compound is prepared from (S)-4-[5-(1 -methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carboxylic acid tert-butyl ester (Intermediate 40; the configuration of the stereocenter is arbitrarily assigned) following a procedure analogous to that described for Intermediate 9. LC (method 7): 1r = 0.48 min; Mass spectrum (ESI⁺): m/z = 378 [M+Hf.

Intermediate 42 (S)“4-r5“(1-Methanesulfonvl-1,2,3,6-tetrahYdro-pyridin-4-vl)-2-methyl-2,3-dihydrofuro[2,3-c]pvridin-2-vll-piperidine-1-carbonitrile

ΝΞ—n

The title compound is prepared from ( S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 41; the configuration of the stereocenter is arbitrarily assigned) and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method

4): t_R = 0.68 min; Mass spectrum (ESl*): m/z = 403 [M+H]⁺.

Intermediate 43 ( S)-N-Hvdroxy-4-r5-( 1 -methanesulfonyl-1,2,3,6-tetrahvd ro-pyridin-4-vl)-2-methvl-

2,3-dihydro-furo[2_l3-clpvridin-2-vl1-piperidine-1-carboxamidine

The title compound is prepared from (S)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carbonitrile (Intermediate 42; the configuration of the stereocenter is arbitrarily assigned) and hydroxylamine hydrochloride following a procedure analogous to that described for Intermediate 11. LC (method 4): t_R = 0.46 min; Mass spectrum (ES!*): m/z = 436 [M+H]⁺.

Intermediate 44 (/?)-4-[5-(1-Methanesulfonyl-1,2,3,6-tetrahvdro-pyridin-4-vl)-2,3-dihvdro-furo[2,3clPvridine-2-yl1-piperidine-1-carbonitrile

N=+~

The title compound is prepared from (/?)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method 6): t_R = 1.02 min; Mass spectrum (ESl·): m/z = 389 [M+Hf. ysJ''

Intermediate 45 (F?)-N-Hydroxy-4-f5-(1-methanesulfonvl-1.2,3.6-tetrahvdro-pyridin-4-vl)-2,3dihvdro-furor2,3-clpyridin-2-vl1-piperidine-1-carboxamidine

The title compound is prepared from (R)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridine-2-yl]-piperidine-1carbonitrile (Intermediate 44, the configuration of the stereocenter is arbitrarily assigned) and hydroxylamine hydrochloride following a procedure analogous to that described for Intermediate 11. LC (method 6): t_R = 0.75 min; Mass spectrum (ESl·): m/z = 422 [M+H]⁺.

Intermediate 46 (S)-4-[5“(1-Methanesulfonvl-1,2,3,6-tetrahvdro-pvridin-4-yl)-2,3-dihvdro-furor2,3-

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 37, the configuration of the stereocenter is arbitrarily assigned) and bromonitrile following a procedure analogous to that described for Intermediate 5. LC (method 6): t_R = 1.02 min; Mass spectrum (ESI⁺): m/z = 389 [M+H]⁺.

Intermediate 47 (S)-N-Hydroxy-4“[5-(1-methanesulfonvl-1,2,3,6-tetrahydro-pyridin-4-yl)-2,3dihvdro-furor2,3-clpyridin-2-yl1-piperidine-1-carboxamidine v<z

The title compound is prepared from (S)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridine-2-yl]-piperidine-1carbonitrile (Intermediate 46, the configuration of the stereocenter is arbitrarily assigned) and hydroxylamine hydrochloride following a procedure analogous to that described for Intermediate 11. LC (method 6): îr = 0.75 min; Mass spectrum (ESI⁺): m/z = 422 [M+H]⁺.

Intermediate 48

4-(5-Bromo-2.3-dihvdro-benzofuran-2-vl)-piperidine

Potassium carbonate (10.17 g) is added to an ice-cooled mixture of 1-[4-(5bromo-2,3-dihydro-benzofuran-2-yl)-piperidin-1-yl]-2,2,2-trifluoro-ethanone (4.64 g), methanol (120 mL), and water (30 mL). The reaction mixture is stirred over night at room température. Brine (150 mL) is added and the mixture is extracted with dichloromethane. The combined organic phases are dried over MgSO₄ and concentrated in vacuo. The crude product is used for the next step without further purification. LC (method 2): t_R = 1.05 min; Mass spectrum (ESI⁺): m/z = 282, 284 [M+H]⁺.

Intermediate 49

4-(5-Bromo-2,3-dihvdro-benzofuran-2-vl)-piperidine-1 -carboxylic acid tert-butyl ester

A mixture of 4-(5-bromo-2,3-dihydro-benzofuran-2-yl)-piperidine (2.37 g) and ditert-butyl dicarbonate (1.83 g) in tetrahydrofuran (25 mL) is stirred for 4 h at room température. The solvent is evaporated in vacuo and the residue is

100 chromatographed on silica gel (cyclohexane/ethyl acetate 90:10 -> 40:60) to give the title compound. TLC: r_f = 0.40 (silica gel, cyclohexane/ethyl acetate 4:1 ); Mass spectrum (ESI*): m/z = 382, 384 [M+H]⁺

Intermediate 50

4-(2-Piperidin-4-vl-2,3-dihydro-benzofuran-5-vl)-benzoic acid methyl ester

HN

To a mixture of 4-(5-bromo-2,3-dihydro-benzofuran-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (1.00 g) and 4-(methoxycarbonyl)phenyl boronic acid (565 mg) in N,N-dimethylformamide (50 mL) a 2 M aqueous Na₂CO₃ solution (3.27 mL) is added. The mixture is sparged with argon for 10 min and PdCI₂[1,Tbis(diphenylphosphino)-ferrocene]-CH₂CI₂ complex (213 mg) is added. The resulting mixture is stirred for 5 h at 90 °C. After cooling to room température water (50 mL) and ethyl acetate (100 mL) are added and the aqueous phase is extracted with ethyl acetate. The organic phase is washed with water and brine, dried over MgSO₄, and the solvent is evaporated.

The residue is mixed with trifluoroacetic acid (1.4 mL), dichloromethane (1.4 mL), and water (0.15 mL) and stirred for 3 h. The solvents are evaporated and the residue is mixed with diethyl ether. The title compound is collected by filtration as the trifluoroacetic acid sait. LC (method 8): t_R = 1.19 min; Mass spectrum (ESI⁺): m/z = 338 [M+H]⁺.

Intermediate 51

4-(2-ri-(5-Ethvl-pvrimidin-2-vl)-piperidin-4-vl1-2,3-dihydro-benzofuran-5-vD-benzoic acid

OH o

101

Ethyldiisopropylamine (1.38 mL) and 2-chloro-5-ethylpyrimidine (380 pL) are added to a solution of 4“(2-piperidin-4-yl-2₁3-dihydro-benzofuran-5-yl)-benzoic acid methyl ester (0.90 g) in tetrahydrofuran (20 mL) and the reaction mixture is heated to reflux for 48 h. The solvent is evaporated after cooling to room température. Dichloromethane and water are added; the aqueous phase is separated and extracted with dichloromethane. The combined organic phases are dried over MgSO₄and the solvent is evaporated. The residue is mixed with methanoi (20 mL) and 1 M aqueous sodium hydroxide solution (6.67 mL). The reaction mixture is stirred at 55°C for 12 h. The solvent is evaporated after cooling to room température. Dichloromethane and water are added; the organic phase is separated and extracted with water. The combined aqueous phases were adjusted to pH 2 with 1 M hydrochloric acid. The title compound is collected by filtration and dried at 50°C in vacuo. LC (method 8): t_R = 1.56 min; Mass spectrum (EST): m/z = 430 [M+H]⁺.

Example 1

S-Ethvl^-H-ÎS-H-methanesulfonvI-phenvD^.S-dihvdro-benzofuran^-vn-piperidin1-vl)-Dvrimidine

Ethyldiisopropylamine (50 pL) and 2-chloro-5-ethylpyrimidine (17 pL) are added to a solution of 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydro-benzofuran-2-yl]piperidine (50 mg) in Ν,Ν-dimethylformamide (1 mL) and the reaction mixture is stirred at 120 °C for 2 h. After cooling to room température over night, dichloromethane and water are added. The aqueous phase is separated and extracted with dichloromethane. The combined organic phases are washed with water, 10% NH₄CI solution, and brine, and dried over MgSO₄.The solvent is evaporated and the residue is triturated with diethyl ether to give the title compound. LC (method 4): t_R = 1.26 min; Mass spectrum (ESI⁺): m/z = 464 vnZ' [M+H]⁺.

102

Example 2

1-(3-lsopropyl-[1,2,4]oxadiazol-5-vl)-4-[5-(4-methanesulfonvl-phenyl)-2.3-dihvdrobenzofuran-2-vri-piperidine

A 0.5 M solution of zinc chloride in tetrahydrofuran (0.78 mL) is diluted with tetrahydrofuran (5 mL) and added dropwise at room température to a mixture of N-hydroxy-isobutyramidine (40 mg) and 4-[5-(4-methanesulfonyl-phenyl)-2,3dihydro-benzofuran-2-yl]-piperidine-1-carbonitrile (100mg) in ethyl acetate (5 mL). The reaction mixture is stirred at 50 °C for 4 h and cooled to room température. The precipitate is filtered off and heated to 100 °C for 2 h in a mixture of éthanol (5 mL) and glacial acetic acid (2.5 mL). The solvents are evaporated and the residue is mixed with dichloromethane and 10% aqueous K2CO3 solution. The organic phase is washed with brîne, dried over MgSO₄ and concentrated in vacuo. The residue is triturated with diethyl ether to give the title compound. LC (method

2): îr = 1.12 min; Mass spectrum (ESI⁺): m/z = 468 [M+H]⁺.

Example 3 1-(3-Cvclopropyl-[1,2,41oxadiazol-5-yl)-4-[5-(4methanesulfonvl-phenyl)-2,3dihvdro-benzofuran-2-vH-piperidine

The title compound is prepared from 4-[5-(4-methanesulfonyl·phenyl)-2,3-dihydrobenzofuran-2-yl]-piperidine-1-carbonitrile and N-hydroxycyclopropanecarboxamidine following a procedure analogous to that described in

Example 2. LC (method 2): t_R = 1.08 min; Mass spectrum (ESI⁺): m/z = 466 [M+H]⁺.

Example 4

103

4-[5-(4-Methanesulfonvl-phenyl)-2,3-dihvdro-benzofuran-2-vl1-1-(3-propyl[1,2,41oxadiazol-5-yl)-piperidine

The title compound is prepared from 4“[5-(4-methanesulfonyl-phenyl)-2,3-dihydrobenzofuran-2-yl]-piperidine-1-carbonitrile and N-hydroxy-butyramidine following a procedure analogous to that described in Example 2. LC (method 2): t_R = 1.40 min; Mass spectrum (ESl·): m/z = 468 [M+H]⁺.

Example 5

2-ri-(5-Ethvl-pyrimidin-2-yl)-piperidin-4-vll-5-(4-methanesulfonvl-phenyl)-2,3dihvdro-furo[2,3-clpyridine

The title compound is prepared from 5-(4-methanesulfonyl-phenyl)-2-piperidin-4yl-2,3-dihydro-furo[2,3-c]pyridine and 2-chloro-5-ethylpyrimidine following a procedure analogous to that described in Example 1. LC (method 5): t_R = 1.14 min; Mass spectrum (ESl·): m/z = 465 [M+H]⁺.

Example 6

2-[1-(3-lsopropyl41,2,41oxadiazol-5-vl)-piperidin-4-yll-5-(4-methanesulfonvlphenYl)-2,3-dihydro-furo[2,3-c]pyridine

The title compound is prepared from 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydrofuro[2,3-c]pyridin-2-yl]“piperidine-1-carbonitrile and N-hydroxy-isobutyramidine

104 following a procedure analogous to that described in Example 2. LC (method 5): t_R = 1.15 min; Mass spectrum (ESI⁺): m/z = 469 [M+Hf.

Example 7

5-(4-Methanesulfonvl-phenvl)-2-[1-(3-propvl-[1.2.4loxadiazol-5-vl)-piperidin-4-vn-

2.3-dihvdro-furor2,3-c1pyridine

The title compound is prepared from 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydrofuro[2,3-c]pyridin-2-yl]-piperidine-1 -carbonitrile and N-hydroxy-butyramidine following a procedure analogous to that described in Example 2. LC (method 5): t_R = 1.15 min; Mass spectrum (ESf): m/z = 469 [M+Hf.

Example 8

2-[1-(5-lsopropyl-[1,2,41oxadiazol-3-vl)-piperidin-4-vl1-5-(4-methanesulfonylphenvl)-2,3-dihvdro-furo[2.3-clpvridine

A mixture of N-hydroxy-4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydro-furo[2,3c]pyridin-2-yl]-piperidine-1-carboxamidine (45 mg), isobutyryl chloride (12 pL), and triethylamine (50 pL) in tetrahydrofuran (5 mL) is stirred for 30 min at room température prior to heating to 80°C for 5 h. The heating is continued over night at reflux. The reaction mixture is diluted with ethyl acetate after cooling to room température, washed with water and brine, dried over MgSO^ and concentrated in vacuo. The residue is triturated with a small amount of methanol and the precipitate is filtered off, washed with diethyl ether, and dried to give the title compound. LC (method 5): t_R = 1.30 min; Mass spectrum (ESf): m/z = 469 [M+Hf.

105

Example 9

5-(4-ΜθΐΚ3ηΘ3υ1ίοην1-ρΚθηνΙ)-2-[1-(5-ρΓθργΙ41,2,41οχ3€ΐί3ζοί-3-νΙ)-ρίρ6πάίη-4-γ11-

2,3-dihvdrO“furo[2,3-clpyridine

The title compound is prepared from N-hydroxy-4-[5-(4-methanesulfonyl-phenyl)~

2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxamidine and butyryl chloride following a procedure analogous to that described in Exemple 8. LC (method 5): t_R = 1.30 min; Mess spectrum (ESI⁺): m/z = 469 [M+H]⁺.

Example 10

5-(4-Methanesulfonyl-Dhenvl)-2-M-(5-methyl-pyrazin-2-yl)-piperidin-4-yll-2,3dihydro-furor2,3clpyridine

A mixture of 5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3c]pyridine (50 mg), 2-chloro-5-methylpyrazine (30 mg), and césium carbonate (91 mg) in dimethylsulfoxîde (1 mL) is heated to 150°C in a microwave oven. After cooling to room température the reaction mixture is diluted with water and extracted with ethyl acetate. The combined extracts are washed with brine, dried over MgSCU, and concentrated in vacuo. The residue is chromatographed on silica gel (ethyl acetate/methanol 98:2—► 97:3). The crude product is triturated with a small amount of methanol and the precipitate is filtered off, washed with diethyl ether, and dried to give the title compound. LC (method 5): t_R - 1.08 min; Mass spectrum (ESI⁺): m/z = 451 [M+H]⁺.

Example 11

106

2-[1-(5-Ethvl-pvrazin-2Vl)-piperidin-4-vl1-5-(4-methanesulfonvl-phenyl)-2,3dihvdro-furof2,3-clpyridine

The title compound is prepared from 5-(4-methanesulfonyl-phenyl)-2-piperidin-4yl-2,3-dihydro-furo[2,3-c]pyridine and 2-bromo-5-ethylpyrazine in N,Ndimethylformamide following a procedure analogous to that described in Example

10. LC (method 5): tR = 1.25 min; Mass spectrum (ESI*): m/z = 465 [M+Hf.

Example 12

2-[1-(5-Ethvl-pvrimidin-2-vl)-piperidin-4-vlT5-(4-methanesulfonvlmethvl-phenyl)-

2,3-dihydro-furof2,3-c1pyridine

The title compound is prepared from 5-(4-methanesulfonylmethyl-phenyl)-2piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and 2-chloro-5-ethylpyrimidine following a procedure analogous to that described in Example 1. LC (method 6): t_R = 1.55 min; Mass spectrum (ESI*): m/z = 479 [M+H]⁺.

Example 13

2-ri-(3-lsopropvl-rL2,4]oxadiazol-5-vl)-piperidin-4-yn-5-(4-methanesulfonylmethvlphenvl)-2,3-dihvdro-furo[2,3-c1pyridine

The title compound is prepared from 4-[5-(4-methanesulfonylmethyl-phenyl)-2,3“ dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile and N-hydroxy

107 isobutyramidine following a procedure analogous to that described in Example 2.

LC (method 6): t_R = 1.46 min; Mass spectrum (ESf): m/z = 483 [M+H]⁺.

Example 14

5-(4-Methanesulfonvl-phenyl)-2-[1 -(3-trifluoromethyl-[1,2,41oxadiazol-5-yl)-

The title compound is prepared from 4-[5-(4-methanesulfonyl-phenyl)-2,3-dihydrofuro[2,3-c]pyridin-2-yl]-piperidine-1 -carbonitrile and 2,2,2-trifluoro-N-hydroxyacetamidine following a procedure analogous to that described in Example 2. LC (method 5): t_R = 1.32 min; Mass spectrum (ESf): m/z = 495 [M+H]⁺.

Example 15

5-(4-Methanesulfonylmethvl-phenvl)-2-[1-(3-propyl-[1,2,4loxadiazol-5-vl)-piperidin4-vl1-2_t3-dihvdro-furof2,3-clpyridine

The title compound is prepared from 4-[5-(4-methanesulfonylmethyl-phenyl)-2,3dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carbonitrile and N-hydroxybutyramidine following a procedure analogous to that described in Example 2. LC (method 6): t_R = 1.46 min; Mass spectrum (ESI*): m/z = 483 [M+Hf.

Example 16

2-M-(5-lsopropvlri,2,41oxadiazol-3-vl)-piperidin-4-vl1-5-(4-methanesulfonvlmethylphenvl)-2,3-dihydro-furo[2,3-c1pvridine

108

The title compound is prepared from N-hydroxy-4-[5-(4-methanesulfonylmethylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxamidine and isobutyryl chloride following a procedure analogous to that described in Example

8. LC (method 6): t_R = 1.54 min; Mass spectrum (ESI⁺): m/z = 483 [M+H]⁺.

Example 17

5-(4-Methanesulfonvlmethvl-phenvl)-2-[1-(5-propyl-n ,2,41oxadiazol-3-yl)-piperidin4-vl]-2,3-dihydro-furoi2_l3-clpvridine

The title compound is prepared from N-hydroxy-4-[5-(4-methanesulfonylmethylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxamidine and butyryl chloride following a procedure analogous to that described in Example 8. LC (method 6): t_R = 1.52 min; Mass spectrum (ESI⁺): m/z = 483 [M+H]⁺.

Example 18

2-[1-(5-Ethvl-pvrimidin-2-vlÎ-piperidin-4-yll-5-(1-methanesulfonyl-1,2,3,6tetrahydro-pvridin-4-vl)-2,3-dihvdro-furor2,3-c]pvridine

The title compound is prepared from 5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and 2-chloro-5ethylpyrimidine following a procedure analogous to that described in Example 1. LC (method 5): t_R = 0.91 min; Mass spectrum (ESI⁺): m/z = 470 [M+H]⁺.

Example 19

5-( 1 -Methanesulfonvl-1,2,3,6-tetrahYdro-pyridin-4-yl)-2-[ 1 -(3-propylri,2,41oxadiazol-5-vl)-piperidin-4-vll-2,3-dihvdro-furo[2,3-clpyridine

109

The title compound is prepared from 4-(5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2_f3“dihydro-furo[2,3-c]pyridin-2-yl]-pipertdine-1-carbonitrile and Nhydroxy-butyramidine following a procedure analogous to that described in Example 2. LC (method 5): t_R = 1.02 min; Mass spectrum (ESI⁺): m/z = 474 [M+H]⁺.

Example 20

2-f1-(3-lsopropvl-ri,2_l41oxadiazol-5-vl)-piperidin-4-yl1-5-(1-methanesulfonvl-

1,2,3,6-tetrahvdro-pvridin-4-vl)-2,3-dihvdro-furoÎ2.3-c1pyridine

The title compound is prepared from 4-(5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carbonitrile and Nhydroxy-isobutyramidine following a procedure analogous to that described in Example 2. LC (method 5): t_R = 1.02 min; Mass spectrum (ESI*): m/z = 474 [M+Hf.

Example 21

5-(2-Fluoro-4-methanesulfonvlmethvl-phenvl)-2-[1-(3-isopropyl-[1,2,41oxadiazol-5vl)-piperidin-4-vl1-2,3-dihvdro-furo[2,3-c1pvridine

The title compound is prepared from 4-[5-(2-fluoro-4-methanesulfonylmethylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carbonitrile and Nhydroxy-isobutyramidine following a procedure analogous to that described in

110

Example 2. LC (method 6): îr = 1.53 min; Mass spectrum (ESl·): m/z = 501 [M+Hf.

Example 22

2-ri-(5-lsopropvl-[1,2,4loxadiazol-3-vl)-piperidin-4-yH-5-(1-methanesulfonvl-

The title compound is prepared from N-hyd roxy-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carboxamidine and isobutyryl chloride foliowing a procedure analogous to that described in Example 8. LC (method 5): îr = 1.08 min; Mass spectrum (ESl⁺): m/z = 474 [M+Hf.

Example 23

5-(1-Methanesulfonyl-1,2,3,6-tetrahvdro-pvridin-4-vl)-2-f1-(5-propyl-

The title compound is prepared from N-hydroxy-4-[5-(1 -methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2₁3-c]pyridin-2-yl]-piperidine-1carboxamidine and butyryl chloride foliowing a procedure analogous to that described in Example 8, LC (method 5): tR = 1.10 min; Mass spectrum (ESI⁺); m/z = 474 [M+Hf.

Example 24

5-(2-Fluoro-4-methanesulfonylmethyl-phenvl)-2-[1-(5-isopropyl-[1,2,4loxadiazol-3vl)-piperidin-4-vll-2,3-dihvdro-furo[2,3-clpyridine

111

The title compound is prepared from 4-[5-(2-fluoro-4-methanesulfonylmethylphenyl)“2,3-dihydro-furo[2,3-c]pyridin-2-yl]-N-hydroxy-piperidine-1-carboxarnidine and isobutyryl chloride following a procedure analogous to that described in Example 8. LC (method 6): îr = 1.59 min; Mass spectrum (ESI⁺): m/z = 501 [M+H]⁺.

Example 25

5-(2-Fluoro-4-methanesulfonylmethvl-phenvl)-2-ri-(5-propvt-f1.2.4loxadiazol-3-vl)piperidin-4-vl1-2,3-dihvdro-furof2,3clpyridine

The title compound is prepared from 4-[5-(2-fluoro-4-methanesulfonylmethyl· phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-N-hydroxy-piperidine-1“Carboxamidine and butyryl chloride following a procedure analogous to that described in Example 8, LC (method 6): t_R = 1.58 min; Mass spectrum (ESI⁺): m/z = 501 [M+H]\

Example 26 (S)-2-[1-(3-lsopropyl-f1.2,4loxadiazol-5-yl)-piperidin-4-yl1-5-(4-methanesulfonvlphenvl)-2-methyl-2,3-dihydro-furo[2,3-c1pyridine

The title compound is prepared from (S)-4-[5-(4-methanesulfonyl-phenyl)-2methyl-2_l3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile (Intermediate 33; the configuration of the stereocenter is arbitrarily assigned) and N-hydroxy- <*7

112 isobutyramidine following a procedure analogous to that described in Example 2. LC (method 4): îr = 1.13 min; Mass spectrum (ESI⁺): m/z = 483 [M+H]⁺.

Example 27 (S)-(5-(4-Methanesulfonvl-phenvl)-2-methvl-2-[1-(3-propyl-(1,2,4loxadiazol-5-vl)piperidin-4-vl]-2,3-dihydro-furo|2.3-clpvridine

The title compound is prepared from (S)-4-[5-(4-methanesulfonyl-phenyl)-2methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile (Intermediate 33; the configuration of the stereocenter is arbitrarily assigned) and N-hydroxybutyramidine following a procedure analogous to that described in Example 2. LC (method 6): tR - 1.25 min; Mass spectrum (EST): m/z = 483 [M+H]*.

Example 28 (S)-2-ri-(5-Ethvl-pvrimidin-2-vl)-piperidin-4-vl1-5-(4-methanesulfonvl-phenyl)-2-

The title compound is prepared from (S)-5-(4-methanesulfonyl-phenyl)-2-methyl-2piperidin-4-yl-2,3“dihydro-furo[2,3-c]pyridine (Intermediate 32; the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5-ethylpyrimidine in dimethylsulfoxide at 105°C in the presence of potassium carbonate. LC (method 4): îr = 1.09 min; Mass spectrum (ESI⁺): m/z = 479 [M+H]⁺.

Example 29 (S)-241-(3-tert-Butvl-ri.2.4]oxadiazol-5-vl)-piperidin-4-yll-5-(4-methanesuifonvl·· phenvl)-2-methyl-2.3-dihvdro-furo[2,3-c]pvridine

113

The title compound is prepared from (S)-4-[5-(4-methanesulfonyl-phenyl)-2methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile (Intermediate 33; the configuration ofthe stereocenter is arbitrarily assigned) and N-hydroxy2,2-dimethyl-propionamidine following a procedure analogous to that described in Example 2. LC (method 4): t_R = 0.93 min; Mass spectrum (ESf ): m/z = 497 [M+Hf.

Example 30 (S)-2-[1-(5“Ethvl-pvrimidin-2-vl)-piperidin-4-vl1-5-(1-methanesulfonyl-1,2,3,6-

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 37, the configuration ofthe stereocenter is arbitrarily assigned) and 2-chloro-5ethylpyrimidine following a procedure analogous to that described in Example 1. LC (method 5): îr = 0.87 min; Mass spectrum (ESf): m/z = 470 [M+Hf.

Example 31 (_ÎR)-2-[1-(5-Ethvl-pvrimidin-2-vl)-pioeridin-4-yl]-5-M-inethanesulfonvl-1,2,3,6tetrahvdro-pvridin-4-yl)-2,3-dihvdro-furo[2,3-clpyridine o

114

The title compound is prepared from (/?)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5ethylpyrimidine following a procedure analogous to that described in Example 1. LC (method 5): t_R = 0.87 min; Mass spectrum (ESI*): m/z = 470 [M+H]⁺.

Example 32 (S)-5-(1-Methanesulfonyl-1,2,3,6-tetrahvdro-pvridin-4-vl)-2-[1-t'5-methyl-Dvrimidin2-vl)-piperidin-4-vll-2.3-dihvdro-furo|2,3-clpyridine

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 37, the configuration of the stereocenter is arbitrarily assigned) and 2-bromo-5methylpyrimidine following a procedure analogous to that described in Example 1. LC (method 5): t_R = 0.84 min; Mass spectrum (ESl⁺): m/z = 456 [M+H]⁺.

Example 33 (F?)-5(1-Methanesulfonvl-1,2,3,6-tetrahydro-pvridin-4-vl)-2-i1-(5-methvl-pyrimidin2-yl)-piperidin-4-yl1-2₁3-dihvdro-furo[2,3-

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2-bromo-5methylpyrimidine following a procedure analogous to that described in Example 1.

LC (method 5): t_R = 0.84 min; Mass spectrum (ESI*): m/z = 456 [M+H]⁺.

115

Example 34

2-i1-(3-tert-Butvl-F1,2,4loxadÎazol-5-vl)-piperidin-4-vn-5-(1-methanesulfonyl-

1,2,3,6-tetrahvdro-pvridin-4-vl)-2,3-dihvdro-furoF2,3- clpyridine

The title compound is prepared from 4-[5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin~4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile and Nhydroxy-2,2-dimethyl-propionamidine foilowing a procedure analogous to that described in Example 2. LC (method 6): t_R = 1.51 min; Mass spectrum (ESI⁺): m/z - 488 [M+H]⁺.

Example 35 ($)-5-(1-Methanesulfonvl-1,2,3,6-tetrahvdro-pyridin-4-yl)-2-methvl-2-f1-(5trifluoromethvl-pvrimidin-2-vl)-piperidin-4-vl1-2,3-dihydro-furor2,3-clpvridine

The title compound is prepared from (SJ-S-il-methanesulfonyl-I^.S.G-tetrahydropyridin-4-yl)-2-methyl-2“piperidin-4-yl-2,3-dihydro-furo[2₁3-c]pyridine (Intermediate 41 ; the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5(trifluoromethyl)pyrimidïne in dimethylsulfoxide at 105°C in the presence of potassium carbonate. LC (method 4): t_R = 1.14 min; Mass spectrum (ESI⁺): m/z 524 [M+H]⁺.

Example 36 ($)-2-F1-(5-Ethvl-pvrimidin-2-vl)-piperidÎn-4-yl1-5-(1-methanesulfonvl-1,2,3,6 tetra hyd ro-p vrid i n-4-vl )-2-meth yl-2,3-d i h yd rofu rof 2,3-cl pyrid i ne

116

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-methyl-2-piperidin-4-yl-2₁3-dihydro-furo[2,3-c]pyridine (Intermediate 41 ; the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5ethyl-pyrimidine in dimethylsulfoxide at 105°C in the presence of potassium carbonate. LC (method 4): t_R = 0.91 min; Mass spectrum (ESf ): m/z = 484 [M+Hf.

Example 37 (5)-5-(1-Methanesulfonvl-1.2,3,6-tetrahydro-pyridin-4-vl)-2-methvl-2-[1-(5trifluoromethvl-pvridin-2-vl)-piperidin-4-vl]-2,3-dihvdro-furo[2,3-c]pvridine

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 41; the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5(trifluoromethyl)pyridine in dimethylsulfoxide at 100°C in the presence of potassium carbonate. LC (method 4): t_R = 1.04 min; Mass spectrum (ESf): m/z = 523 [M+Hf.

Example 38

117 (5)-5-(1-Methanesulfonyl-1,2,3.6-tetrahvdro-pvridin-4-yl)-2-methvl-2-ri-(5trifluoromethvl-pvrazin-2-vl)-piperidin-4-vl]-2,3-dihvdro-furo[2,3clpyridine

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro pyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate ; the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5 (trifluoromethyl)pyrazine in dimethylsulfoxide at 100°C in the presence of potassium carbonate. LC (method 4): t_R = 1.06 min; Mass spectrum (ESI⁺): m/z = 524 [M+Hf.

Example 39

2-[1-(5-tert-Butvl-[1_l2,4]oxadiazol-3-yl)-piperidin-4-vn-5-(1-methanesulfonvl-

1,2,3,6-tetrahvdro-pvridin-4-vl)-2,3-dihvdro-furo[2,3-c1pyridine

A mixture of N-hydroxy-4-[5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-

2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxamidine (30 mg) and trimethylacetic anhydride (30 μΙ) in toluene (2 mL) is heated under reflux for 2 h. The reaction mixture is concentrated in vacuo and chromatographed on silica gel (cyclohexane/ethyl acetate = 50:50). The crude product is triturated with diethyl ether, filtered off, and dried to give the title compound. LC (method 6): t_R = 1.58 min; Mass spectrum (EST): m/z = 488 [M+Hf.

Example 40 (S)-5-(1-Methanesulfonyl-1,2,3,6-tetrahydro-pvridin-4-vl)-2-methvl-2-[1-(3-fluor-5triftuoromethvl-pvridin-2-vl)-piperidin-4-vll-2.3-dihvdro-furor2,3-clpyridine

118

F

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2_I3-c]pyridine (Intermediate 41; the configuration of the stereocenter is arbitrarily assigned) and 2-bromo-3fluoro-5-(trifluoromethyl)pyridine in dimethylsulfoxide at 100°C in the presence of potassium carbonate. LC (method 4): îr = 1.21 min; Mass spectrum (ESl·): m/z = 541 [M+H]⁺.

Example 41 (S)-5-(1-Methanesulfonvl-1,2.3.6-tetrahvdro-pyridin-4-vl)-2-methyl-241-(5-methvlpyrimidin-2-ylÎ-piperidin-4-vll-2,3-dihvdro-furo[2,3-clpyridine

The title compound is prepared from ($)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-A-yl^-methyl^-piperidin^-yl^.S-dihydro-furop.S-cjpyridine (Intermediate 41; the configuration of the stereocenter is arbitrarily assigned) and 2-bromo-5methyl-pyrimidine in dimethylsulfoxide at 100°C in the presence of potassium carbonate. LC (method 4): t_R = 0.81 min; Mass spectrum (ESl·): m/z = 470 [M+H]⁺.

Example 42 (S^-ri-O-lsopropyl-ri^^loxadiazol-S-vD-piperidin^-yll-S-fl-methanesulfonyl-

1,2,3,6-tetrahvdro-pyridin-4-vl)-2-methyl-2,3-dihydro-furoF2,3-clpvridine

119

The title compound is prepared from (S)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carbonitrile (Intermediate 42; the configuration of the stereocenter is arbitrarily assigned) and N-hydroxy-isobutyramidine following a procedure analogous to that described in Example 2. LC (method 4): îr = 0.97 min; Mass spectrum (ESI⁺): m/z = 488 [M+H]⁺.

Example 43 (S)-2-ri-(5-lsopropvl-[1.2.41oxadiazol-3-vl)-piperidin-4-vl1-5-(1-methanesulfonyl-

1,2.3.6-tetrahvdro-pvridin-4-vl)-2-methvl-2,3-dihydro-furo[2,3-clDvridine

The title compound is prepared from (S)-N-hydroxy-4-[5-(1-methanesulfonyl1,2_t3,6-tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2_I3-c]pyridin-2-yl]piperidine-1-carboxamidine (Intermediate 43; the configuration ofthe stereocenter is arbitrarily assigned) and isobutyryl chloride following a procedure analogous to that described in Example 8. LC (method 4): t_R = 1.01 min; Mass spectrum (ESI⁺): m/z = 488 [M+H]⁺.

Example 44 (R)-5-(1-Methanesulfonvl-1,2,3,6-tetrahydro-pvridin-4-vl)-2-H-(5-propyl[1,2,4loxadiazol-3“yl)-piperidin-4-vll-2,3-dihydro-furor2,3-

The title compound is prepared from (/?)-N-hydroxy-4-[5-(1-methanesulfonyl-

1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carboxamidine (Intermediate 45; the configuration ofthe stereocenter is arbitrarily assigned) and n-butyric anhydride following a procedure analogous to that

120 described in Example 39. LC (method 6): t_R = 1.47 min; Mass spectrum (ESI⁺): m/z = 474 [M+H]⁺.

Example 45 (/?)-2-ri-(5-lsopropyl-ri,2,41oxadiazol-3-vl)-piperidin-4-yl1-5-(1-methanesulfonyl-

1,2,3,6-tetrahvdro-pvridin-4-vl)-2.3-dihydro-furof2,3-

1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carboxamidine (Intermediate 45; the configuration ofthe stereocenter is arbitrarily assigned) and isobutyric anhydride following a procedure analogous to that described in Example 39. LC (method 6): t_R = 1.47 min; Mass spectrum (ESI⁺): _m/z = 474 [M+H]⁺.

Example 46 (S)-2-[1-(5-lsopropvl-ri,2,4loxadiazol-3-vl)-piperidin-4-vH-5-(1-methanesulfonvl-

1,2,3,6-tetrahvdro-pvridin-4-vl)-2,3-dihydro-furo[2.3-

Example 47 clpyridine ^υ

The title compound is prepared from (S)-N-hydroxy-4-[5-(1-methanesulfonylI.Z.S.e-tetrahydro-pyridin-A-yO-Z.S-dihydro-furolZ.S-cjpyridin-Z-ylJ-piperidine-lcarboxamidine (Intermediate 47; the configuration of the stereocenter is arbitrarily assigned) and isobutyric anhydride following a procedure analogous to that described in Example 39. LC (method 6): t_R = 1.47 min; Mass spectrum (ESI⁺):

m/z = 474 [M+H]⁺.

121 (S)-5-(1-Methanesulfonvl-1,2,3,6-tetrahydro-pvridin-4-vl)-2-methvl-2-[1-(5-propvl· [1,2,4loxadiazol-3-yl)-piperidin-4-vll-2,3-dihydro-furo[2,3-c|pyridine

The title compound is prepared from (S)-N-hydroxy-4-[5-(1-methanesulfonyl-

1,2,3,6-tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]piperidine-1-carboxamidine (Intermediate 43; the configuration ofthe stereocenter is arbitrarily assigned) and butyryl chloride following a procedure analogous to that described in Example 8. LC (method 4): t_R = 1.00 min; Mass spectrum (ESI⁺): m/z = 488 [M+Hf.

Example 48

5-(1-Methanesulfonvl-1,2,3,6-tetrahydro-pvridin-4-vl)-2-methvl-2-[1-(5trifluoromethvl-[1,3,4lthiadiazol-2~yl)-piperidin-4-vn-2,3-dihvdro-furor2.3-clpvridine

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-methyl-2-piperidin-4-yl-2₁3-dihydro-furo[2,3-c]pyridine (Intermediate 41 ; the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5trifluoromethyl-[1,3,4]thiadiazole in dimethylsulfoxide at 85°C in the presence of potassium carbonate. LC (method 4): t_R = 0.98 min; Mass spectrum (ESf): m/z = 530 [M+Hf.

Example 49

122 (S)-5-(1-Methanesulfonvi-1.2,3,6-tetrahydro-pyridin-4-yl)-2-ri -(5-propylri,2,41oxadiazol-3-vn-piperidin-4-vn-2,3-dihydro-furo[2,3-

1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1carboxamidine (Intermediate 47; the configuration of the stereocenter is arbitrarily assigned) and n-butyric anhydride following a procedure analogous to that described in Example 39. LC (method 6): t_R = 1.47 min; Mass spectrum (ESl·): m/z = 474 [M+H]⁺.

Example 50 (/?)-2-[1 -(5-tert-Butyl-[1 ,2,4]oxadiazol-3-vl)-piperidin-4-yl]-5-(1 -methanesulfonvl-

1,2,3,6-tetra hyd ro-pyrid i n-4-yl )-2,3-d i hyd ro-furo[2,3-

clpyridine ^u

The title compound is prepared from (R)-N-hydroxy-4-[5-(1-methanesulfonyl-

1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2_l3-c]pyridin-2-yl]-piperidine-1 carboxamidine (Intermediate 45; the configuration of the stereocenter is arbitrarily assigned) and trimethylacetic anhydride following a procedure analogous to that described in Example 39. LC (method 6): t_R = 1.58 min; Mass spectrum (ESl·): m/z = 488 [M+H]⁺.

Example 51

123 (S)-2-[1-(5-tert-Butvl-[1,2,4]oxadiazol-3-yl)-piperidin-4-vl1-5-(1-methanesulfonyl1,2,3,6-tetrahydro-pvridin-4-vl)-2.3-dihydro-furo[2,3-

1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1·' carboxamidine (Intermediate 47; the configuration ofthe stereocenter is arbitrarily assigned) and trimethylacetic anhydride following a procedure analogous to that described in Example 39. LC (method 6): t_R = 1.58 min; Mass spectrum (ESl·): m/z = 488 [M+H]⁺.

Example 52 (S)-5-(1-Methanesulfonvl-1, 2,3,6-tetra hydro-pyrid in-4-yl )-2-11-( 5-trif luoromethylpvrimidin-2-vl)-pÎperidin-4-vn-2,3-dihYdro-furo(2.3-c1pvridine

ifx

O

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 37, the configuration ofthe stereocenter is arbitrarily assigned) and 2-chloro-5(trifluoromethyl)pyrimidine in dimethylsulfoxide at 110°C in the presence of potassium carbonate. LC (method 5): t_R = 1.28 min; Mass spectrum (ESl·): m/z = 510 [M+H]⁺.

Example 53 \>Z

124 (S)-5-(1-Methanesulfonvl-1 ^.e.e-tetrahvdro-pyridin^-vD^-methyl^-fl-fS-methvlPvrazin-2-vl)-piperidin-4-vll-2,3-dihvdro-furo[2,3-clpvridine

The title compound is prepared from (S)-5-(1-methanesulfor)yl-1,2,3,6-tetrahydropyridin-4-yl)-2-methyl-2-piperïdin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 41; the configuration of the stereocenter is arbitrarily assigned) and 2-bromo-5methyl-pyrazine in dimethylsulfoxide at 125°C in the presence of potassium carbonate. LC (method 4): t_R = 0.84 min; Mass spectrum (ESΓ): m/z = 470 [M+Hf.

Example 54 (/?)-5-(1-Methanesulfonyl-1.2,3.6-tetrahvdro-pvridin-4-vl)-2-i1-[5-(1-methylcyclopropvl)-[1,2,4]oxadiazol-3-vll-piperidin-4-vl)-2,3-dihvdro-furo[2,3-clpyridine

The title compound is prepared from (Z?)-N-hydroxy-4-[5-(1~methanesulfonyl-

1,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 carboxamidine (Intermediate 45; the configuration of the stereocenter is arbitrarily assigned) and 1-methyl-cyclopropanecarbonyl chloride following a procedure analogous to that described in Example 8. LC (method 6): t_R = 1.53 min; Mass spectrum (ESf): m/z = 486 [M+Hf.

Example 55 (S)-2-[1-(3-Îsopropvl-i1,2,41oxadiazol-5-vl)-piperidin-4-yll-5-(1-methanesulfonvl·

1,2,3,6-tetrahvdro-pyridin-4-vlL2,3-dihvdro-furo[2,3-c1pyridine —

125

The title compound is prepared from (S)-4-[5-(1 -methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridine-2-yl]-piperidine-1carbonitrile (Intermediate 46; the configuration ofthe stereocenter is arbitrarily assigned) and N-hydroxy-isobutyramidine following a procedure analogous to that described in Example 2. LC (method 6): t_R = 1.40 min; Mass spectrum (ESI*): m/z = 474 [M+H]⁺.

Example 56 (S)-2-ri-(5-Chloro-pvrimidin-2-vl)-piperidin-4-vll-5-(4-methanesulfonvl-phenvl)-2-

The title compound is prepared from (S)-5-(4-methanesulfonyl-phenyl)-2-methyl-2piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 32; the configuration of the stereocenter is arbitrarily assigned) and 2,5-dichloro-pyrimidine in dimethylsulfoxide at 105°C in the presence of potassium carbonate. LC (method

6): t_R = 1.78 min; Mass spectrum (ESI*): m/z = 485 [M+H]⁺.

Example 57 (S)-5-(1-Methanesulfonvl-1,2,3,6-tetrahvdro-pvridin-4-vl)-2-(1-l5-(1-methylcyclopropyl)-[1₁2,4]oxadiazol-3-vl1-piperidin-4-vl}-2,3-dihvdro-furo[2.3-clpyridine

The title compound is prepared from (S)-N-hydroxy-4-[5-(1-methanesulfonyl1 ,2,3,6-tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-116478

126 carboxamidine (Intermediate 47; the configuration of the stereocenter is arbitrarily assigned) and 1-methyl-cyclopropanecarbonyl chloride following a procedure analogous to that described in Example 8. LC (method 6): t_R = 1.53 min; Mass spectrum (ESI⁺): m/z = 486 [M+H]⁺.

Example 58 (S)-2-ri-(5-Chloro-Dvrimidin-2-vl)-piperidin-4-vn-5-(1-methanesulfonyl-1,2,3,6tetrahvdro-pvridin-4-vl)-2-methvl-2₁3-dihvdro-furo[2,3-c1pyridine

The title compound is prepared from (SJ-S-O-methanesulfonyl-I^.S.e-tetrahydropyridin-4-yl)-2-methyl-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 41; the configuration of the stereocenter is arbitrarily assigned) and 2,5-dichloropyrimidine in dimethylsulfoxide at 105°C in the presence of potassium carbonate. LC (method 6): t_R = 1.78 min; Mass spectrum (ESI⁺): m/z = 490 [M+H]⁺,

Example 59 (/?)-2-H -(3-lsopropvl-fl .2,4]oxadiazol-5-vl)-piperidin-4-yll-5-( 1 -methanesulfonyl-

1.2.3.6-tetrahvdro-pvridin-4-yl)-2,3-dihydro-furoi2,3-c]pvridine

Example 60

O

The title compound is prepared from (/?)-4-[5-(1-methanesulfonyl-1,2,3,6tetrahydro-pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridine-2-yl]-piperidine-1carbonitrile (Intermediate 44; the configuration of the stereocenter is arbitrarily assigned) and N-hydroxy-isobutyramidine following a procedure analogous to that described in Example 2. LC (method 6): t_R = 1.40 min; Mass spectrum (ESI⁺): m/z = 474 [M+H]⁺.

127 (4-(241 -(5-Ethyl-pyrinnidin-2-vl)-piperidin-4-vl1-2,3-dihvdro-benzofuran-5-yl}-

To a mixture of 4-{2-[1-(5-ethyl-pyrïmidin-2-yl)-piperidin-4-yl]-2,3-dihydro5 benzofuran-5-yl}-benzoic acid (43 mg) in A/,/V-dimethylformamide (1.5 mL) diethylisopropylamine (52 pL) and 2-(1 H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU, 32 mg) are added. After 10 min morpholine (11 mg) in Λ/,/V-dimethylformamide (0.5 mL) is added. The mixture is stirred for 12 h and purified by préparative HPLC (eluent water (+0.1% TFA)/methanol) to yield the desired product. HPLC (method 9): t_R = 1.95 min; Mass spectrum (ESI*): m/z = 499 [M+Hf.

The following compounds of general formula (1-1 ) are prepared analogously to

Example 60, the starting materials used being shown in the column headed SM

1:

Ex.	R	SM 1	ESI-MS [m/z] [M+H]+	R((HPLC) [min] (method 6)
61	a. I *	a. H	527	2.01

128

Ex.	R	SM 1	ESI-MS [m/z] [M+Hf	Rt(HPLC) [min] (method 6)
62	I °\ V *	I H	501	1.98
63	L. N H	nh2	515	2.02
64	V.. N H	M ‘HCl Sh2	510	1.92
65	F6F N I *	FÔF *HC. N H	505	2.05
66	OH V N H	Λ nh2	501	1.95
67	n H	t nh2	468	1.91

129

Ex.	R	SM 1	ESI-MS [m/z] [M+Hf	Rt(HPLC) [min] (method 6)
68	OH /	OH t> H	513	1.93
Y *
69	6 1 *	ό H	527	2.02
70	HO *	HCV. 0 H	499	1.86
71	n 1	n H	482	1.92
72	y. N H	? nh2	513	1.99
73	?.. N H	o ήη2	520	1.67

130

Ex.	R	SM 1	ESI-MS [m/z] [M+H]+	R, (HPLC) [min] (method 6)
74	X. N H	^nh2	487	1.92
75	V N H	QH ^>L * HCl ^nh2	515	1.98
76	N I *	'î Z\ * HCl N H	499	1.99
77	N H	Oo *HCI Sh2	529	1.94
78	HO. I	HCL H	487	1.87

Example 79

131 (F?)-5-(1-Methanesulfonvl-1,2,3,6-tetrahvdro-pvridin“4-yl)-2-[1-(5-trifluoromethvlPVrimidin-2-yO-piperidin-4-vll-2,3-dihvdro-furof2,3-clpyridine

Il

O

A mixture of (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-piperidin4-yl-2₁3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned; 110 mg}, 2-chloro-5-trifluoromethyl-pynmidine (76 mg), K2CO3 (100 mg), and dimethyl sulfoxide (1.5 mL) is stirred at 110 °C for 3 h. After cooling to room température, water is added and the resulting mixture is extracted with ethyl acetate. The combined extracts are washed with brine, dried (Na₂SO₄), and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 30:70->10:90) to give the title compound. LC (method

5): t_R = 1.32 min; Mass spectrum (ESI*): m/z = 510 [M+H]*.

Example 80 (/^:?)-5-(1-Methanesulfonvl·1,2,3,6-tetrahvdro-pvridin-4-yl)-2-|'1-(5-trifluoromethvlPvrazin-2-vl)-piperidin-4-vl1-2.3-dihvdro-furof2,3-c]pvridine

The title compound is prepared from (RJ-ô^l-methanesulfonyl-I^.S.e-tetrahydropyridin-4“yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5trifluoromethyl-pyrazine following a procedure analogous to that described for Example 79. LC (method 7): îr = 1.56 min; Mass spectrum (ESI*): m/z = 510 [M+H]*.

Example 81 (R)-5-(1-Methanesulfonvl-1 ^.S.e-tetrahvdro-pvridin^-vD^-M -(5-trifluoromethylri.3,41thiadiazol-2-vl)-piperidin-4-vl1-2,3-dÎhvdro-furo[2.3-clpyridine

132

The title compound is prepared from (/?)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyrïdin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration ofthe stereocenter is arbitrarily assigned) and 2-chloro-5trifluoromethyl-[1,3,4]thiadiazole following a procedure analogous to that described for Example 79. LC (method 7): t_R = 1.46 min; Mass spectrum (ESf): m/z = 516 [M+Hf.

Example 82 (f?)-4-r5-(1-Methanesulfonvl-1.2,3,6-tetrahvdro-pyridin-4-yl)-2,3-dihydro-furo[2,3clPVridin-2-vn-5^l-trifluoromethvl-3.4,5,6-tetrahydro-2H-[1.2*lbipvridinyl

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration ofthe stereocenter is arbitrarily assigned) and 2-chloro-5trifluoromethyl-pyridine following a procedure analogous to that described for Example 79. LC (method 7): t_R = 1.63 min; Mass spectrum (ESΓ): m/z = 509 [M+Hf.

Example 83 (/?)-2-[1-(5-Chloro-pvrimidin-2-yl)-piperidin-4-yl1-5-(1-methanesulfonyl-1,2,3,6tetrahvdro-pyridin-4-vl)-2,3-dihydro-furo[2,3-clpyridine

133

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2,5-dichloropyrimidine following a procedure analogous to that described for Example 79. LC (method 7): îr = 1.63 min; Mass spectrum (ESI⁺): m/z = 476/478 (Cl) [M+H]⁺.

Example 84 (/?)-3^l-Fluoro-4-r5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pvridin-4-vl)-2.3-dîhydrofuror2,3-c1pvridin-2-yl1-5^,-trifluoromethvl-3.4.5.6-tetrahvdro-2H-ri,2^l1bipvridinYl

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2-bromo-3-fluoro-5trifluoromethyl-pyridine following a procedure analogous to that described for Example 79. LC (method 7): t_R = 1.75 min; Mass spectrum (ESI⁺): m/z = 527 [M+H]⁺.

Example 85 (F?)-2-[1-(5-Ethvl-pvrimidin-2-vl)-piperidin-4-vl]-5-(4-methanesulfonyl-phenyl )-2,3dihvdro-furor2,3-clpvridine

A mixture of (f?)-5-(4-methanesulfonyl-phenyl)-2-piperidin-4-yl-2,3-dihydrofuro[2,3-c]pyridine {obtained from (/?)-4-[5-(4-methanesulfonyl-phenyl)-2,3dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carboxylic acid tert-butyl ester by cleavage of the carbamate group (following a procedure analogous to that described for Intermediate 9), which in turn is synthesized from Intermediate 34 and 4-methanesulfonyl-phenylboronic acid following a procedure analogous to

134 that described for Intermediate 7, the configuration of the stereocenter is arbitrarily assigned; 110 mg}, 2-chloro-5-ethyl-pyrimidine (52 pL), Ν,Ν-diisopropylethylamine (0.18 mL), and N,N-dimethylformamide (2 mL) is stirred at 120 °C for 5 h. After cooling to room température, water is added and the resulting mixture is extracted with ethyl acetate. The combined extracts are washed with brine, dried (Na2SO₄), and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 40:60-+30:70) to give the title compound. LC (method

6): t_R = 1.65 min; Mass spectrum (ES I*): m/z = 465 [M+H]⁺.

Example 86 (S)-2-f1-(5-Chloro-pvrimidin-2-vl)-piperidin-4-vll-5-(1 -methanesulfonyl-1,2,3,6tetrah yd ro-pyrid i n-4-vl )-2,3-d i h vd ro-fu ro [2,3-c] pyrid i ne

The title compound is prepared from (S)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 37, the configuration of the stereocenter is arbitrarily assigned) and 2,5-dichloropyrimidine following a procedure analogous to that described for Example 79. LC (method 7): t_R = 1.62 min; Mass spectrum (ESI⁺): m/z = 476/478 (Cl) [M+H]⁺.

Example 87 (f?)-2-[1-(5-Chloro-pyrimidin-2-vl)-piperidin-4-vH-5-(4-methanesulfonvl-phenyl )-2,3-

dihvdro-furo[2,3-c1pyridine

The title compound is prepared from (R)-5-(4-methanesulfonyl-phenyl)-2-piperidin4-yl-2,3-dihydro-furo[2,3-c]pyridine {obtained from (R)-4-[5-(4-methanesulfonylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carboxylic acid tert-butyl ester by cleavage of the carbamate group (following a procedure analogous to

135 that described for Intermediate 9), which in turn is obtained from Intermediate 34 and 4-methanesulfonyl-phenylboronic acid following a procedure analogous to that described for Intermediate 7, the configuration of the stereocenter is arbitrarily assigned} and 2,5-dichloro-pyrimidine following a procedure analogous to that described for Example 79. LC (method 6): t_R = 1.63 min; Mass spectrum (ESI⁺): m/z = 471/473 (Cl) [M+H]⁺.

Example 88 (F?)-2-[1-(5-Chloro-pyrimidin-2-yl)“Piperidin-4-vl1-5-(1-methanesulfonvl-1,2,3,6tetra hyd ro-pyrid in-4-vl )-2-meth vl-2,3-d i hyd ro-f uro[2,3-clpyrid ine

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (obtained from 4-(5-(1methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-methyl-2,3-dihydro-furo[2,3c]pyridin-2“yl]-piperidine-1-carboxylic acid tert-butyl ester by cleavage of the carbamate group (following a procedure analogous to that described for Intermediate 9), which in turn is obtained from Intermediate 30 and 1(methylsulfonyl)-4-(4,4₁5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1_l2,3,6tetrahydropyridine following a procedure analogous to that described for Intermediate 7, the configuration of the stereocenter is arbitrarily assigned} and

2,5-dichloro-pyrimidine following a procedure analogous to that described for Example 79. LC (method 4): t_R = 1.08 min; Mass spectrum (ESI*): m/z = 490/492 (Cl) [M+H]⁺.

Example 89 (S)-2-[1-(5-Cvclopropvl-pvrimidin-2-vl)-piperidin-4-yl]-5-(4-methanesulfonvlphenyl)-2-methvl-2,3-dihvdro-furo[2,3-clpyridine

136

The title compound is prepared from (S)-5-(4-methanesulfonyl-phenyl)-2-piperidin4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 32, the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5-cyclopropyl- pyrimidine foliowing a procedure analogous to that described for Example 79. LC (method 4): t_R = 0.95 min; Mass spectrum (ESI⁺): m/z = 496 [M+Hf.

Example 90 (S)-2-[1-(5-Chloro-pyrimidin-2-vl)-piperidin-4-vll-5-(4-methanesulfonyl-phenyl)-2_l3dihvdro-furo[2,3-clpyridine

o

The title compound is prepared from (S)-5-(4-methanesulfonyl-phenyl)-2-piperidin4-yl-2,3-dihydro-furo[2,3-c]pyridine {obtained from (S)-4-[5-(4-methanesulfonyl· phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester by cleavage of the carbamate group (foliowing a procedure analogous to that described for Intermediate 9), which in turn is obtained from Intermediate 35 and 4-methanesulfonyl-phenylboronic acid foliowing a procedure analogous to that described for Intermediate 7, the configuration of the stereocenter is arbitrarily assigned} and 2,5-dichloro-pyrimidine foliowing a procedure analogous to that described for Example 79. LC (method 6): t_R = 1.75 min; Mass spectrum (ESf): m/z = 471/473 (Cl) [M+Hf.

Example 91 (/?)-2-[1-(5-Cvclopropvl-pvrimidin-2-vl)-piperidin-4-yll-5-(1-methanesulfonvl-

1,2,3,6-tetrahvdro-pvridin-4-vl)-2,3-dihvdro-furo[2,3-clpyridine

137

The title compound is prepared from(R)-5-(1 -methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-pÎperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5cyclopropyl-pyrimidine following a procedure analogous to that described for Example 79. LC (method 10): îr = 1.61 min; Mass spectrum (ESI⁺): m/z = 482 [M+H]⁺.

Example 92 (f?)-5-(1-Methanesulfonyl-1,2,3,6-tetrahyd ro-pyrid in-4-yl )-2-[1-( 5-methoxypvrimidin-2-vl)-piperidin-4-vll-2,3-dihydro-furof2,3-c1pyridine

The title compound is prepared from (R)-5-(1-methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine (Intermediate 39, the configuration of the stereocenter is arbitrarily assigned) and 2-chloro-5-methoxypyrimidine following a procedure analogous to that described for Example 79. LC (method 10): t_R = 1.48 min; Mass spectrum (ESI⁺): m/z = 472 [M+H]⁺.

Example 93 (F?)-2-f1“(5-Cvclopropvl-pvrimidin-2-vl)-piperidin-4-yl1-5-(4-methanesu1fony1phenyl)-2,3-dihydro-furof2,3-clpyridine

138

The title compound is prepared from (/?)-5-(4-methanesulfonyl-phenyl)-2-piperidin4-yl-2,3-dihydro-furo[2,3-c]pyridine {obtained from (/?)-4-[5-(4-methanesulfonylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester by cleavage of the carbamate group (following a procedure analogous to that described for Intermediate 9), which in turn is obtained from Intermediate 34 and 4-methanesulfonyl-phenylboronic acid following a procedure analogous to that described for Intermediate 7, the configuration of the stereocenter is arbitrarily assigned} and 2-chloro-5-cyclopropyl-pyrimidine following a procedure analogous to that described for Example 79. LC (method 10): t_R = 1.76 min; Mass spectrum (ESI⁺): m/z = 477 [M+H]⁺.

Example 94 (/?)-5-(4-Methanesulfonyl-phenvl)-2-ri-(5-methoxv-pvrimidin-2-yl)-piperidin-4-vl1-

2,3-dihydro-furor2,3-clpyridÎne

The title compound is prepared from (R)-5-(4-methanesulfonyl-phenyl)-2-piperidin4-yl-2,3-dihydro-furo[2,3-c]pyridine {obtained from (R)-4-[5-(4-methanesulfonylphenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1 -carboxylic acid tert-butyl ester by cleavage of the carbamate group (following a procedure analogous to that described for Intermediate 9), which in turn is obtained from Intermediate 34 and 4-methanesulfonyl-phenylboronic acid following a procedure analogous to that described for Intermediate 7, the configuration of the stereocenter is arbitrarily assigned} and 2-chloro-5-methoxy-pyrimidine following a procedure analogous to that described for Example 79. LC (method 10): t_R = 1.69 min; Mass spectrum (ESI⁺): m/z = 467 [M+H]⁺.

The following compounds are prepared in analogy to the above described examples and other methods known from the literature.

139

Example 95

Example 99

Example 100

Example 101

140

Example 102

Example 103

Example 104

Example 106

Example 107

141

Example 108

142

Important Information

Please be informed that the correct name and structure of example 35 (page 110 of the US-text as filed) is:

(R)-5-(l-Methanesulfonyl-l,2,3,6-tetrahydrO“pyridin-4-yl)-2-methyl-2-[l-(5trifluoromethyl-pyrimidin-2-yl)-piperidin-4-yl]-2,3-dihydro-furo[2,3-cjpyridine

F

As mentioned in the text regarding the example, the configuration of the stereocenter was arbitrarily assigned in the text as filed, because the absolute confiugration was not known at the time of filing. In the meantime, the configuration has been determined by additional experiments, and as it turned out, the correct configuration (given above) is opposite to the one given in the text as filed. The same is true for the other examples prepared from Intermediated 41 as starting material. The Examiner should be informed about this fact at the first suitable occasion during the national phase.

Claims (13)

1. Claims

   1.

   A compound of formula I wherein

   R¹ is selected from the group R¹-G1 consisting of a 5- or 6-membered heteroaromatic ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S; and wherein optionally a second ring may be condensed to said heteroaromatic ring, wherein said second ring is unsaturated or aromatic and 5- or 6-membered and may contain 1, 2 or 3 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -Chk-groups may be optionally replaced by -N(Rⁿ)-, -C(=O)-, -S(=O)- or -S(=O)2-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said heteroaromatic ring and/or second ring independently of each other may be optionally substituted with one or more substituents selected from L^A; and wherein said heteroaromatic ring or said second ring may be optionally substituted with a group R^c; and

   Rⁿ independently of each other is selected from the group R^N-G1 consisting of H, Ci-4-alkyl, Ci-4-alkyl-C(=O)-, and Ci^-alkyl-S(=O)₂-; and

   144

   A is selected from the group A-G1 consisting of a 1,2,3,6-tetrahydropyridin-

   4- yl ring substituted at the N with C₁.4-alkyl-S(=O)₂-, a phenyl ring, and a

   5- or 6-membered heteroaromatic ring which contains 1,2 or 3 heteroatoms independently of each other selected from N, O and S; and wherein optionally a second ring may be condensed to said phenyl ring or heteroaromatic ring, wherein said second ring is unsaturated or aromatic and 5- or 6-membered and may contain 1,2 or 3 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -N(Rⁿ)-, -C(=O)-, -S(=O)- or -S(=O)₂-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said phenyl ring, heteroaromatic ring and/or second ring independently of each other may be optionally substituted with one or more substituents selected from L^A; and wherein said phenyl ring, heteroaromatic ring or second ring may be optionally substituted with a group T; and is selected from the group T-G1 consisting of F, Cl, Br, I, CN, OH, NO₂,

   Ci-e-alkyl-, Ci-₆-alkenyl-, Ci.₆-alkynyl-, C₃.₆-cycloalkyl, Cve-alkyl-O-, C₃.₆cycloalkyl-O-, Cv₆-alkyl-S-, HO-C(=O)-, Ci-6-alkyl-0-C(=O)-, C-M-alkylC(=O)-, C₃-₆-cycloalkyl-C(=O)-, Ci^-alkyl-S(=O)-, Ci.₄-alkyl-S(=O)₂-,

   R^NT2N-C(=O)(Rⁿ)N-, heterocyclyl, heterocyclyl-O-, aryl, aryl-O-, heteroaryl and heteroaryl-O-, wherein each alkyl, alkenyl, alkynyl, and cycloalkyl group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN, OH, Ci-₃-alkyl, C₃-6-cycloalkyl, C1.3alkyl-O-, R^NT1R^NT2N-, R^NT1R^NT2N-C(=O)-, Ci_4-alkyl-S(=O)-, C-M-alkylS(=O)2-, R^NT1R^NT2N-S(=O)2-, aryl, heteroaryl, and heterocyclyl, and

   145 pNT1 wherein aryl dénotés phenyl or naphthyl, and wherein heteroaryl is a 5- or 6-membered aromatic ring which contains 1, 2, 3 or 4 heteroatoms independently of each other selected from N, O and S, wherein the H-atom in one or more NH groups may be optionally replaced by R^N; and wherein heterocyclyl is a 4- to 7-membered unsaturated or saturated carbocyclic ring in which 1 or 2 -CH2-groups independently of each other are replaced by NRⁿ, O, -C(=O)-, S, -S(=O)- or -S(=O)2-, and/or in which a -CH-group is replaced by N; and wherein each aryl, heteroaryl or heterocyclyl group may be optionally substituted with one or more substituents independently of each other selected from L^A; and is selected from the group R^NT1-G1 consisting of H, Ci_e-alkyl, C₃-ecycloalkyl, Ci-6-alkyl-C(=O)-, C₁.₆-alkyl-S(=O)2, heterocyclyl, aryl and heteroaryl, wherein each alkyl and cylcoalkyl group may be optionally substituted with one or more substituents independently of each other selected from the group consisting of F, OH, CN, Ci^-alkyl, Ci.₄-alkyl-O-, R^N2N, Ci-₄-alkylS(=O)₂-, C₃.6-cycloalkyl, heterocyclyl, phenyl and heteroaryl; and wherein heterocyclyl may be optionally substituted with one or more substituents independently of each other selected from F, C-M-alkyl, R^N2N, OH and Ci.₄-alkyl-O-; and wherein heterocyclyl is a C₄_7-cycloalkyl ring in which 1 or 2 -CH2-groups independently of each other are replaced by NRⁿ, O, C(=O), S, S(=O) or S(=O)₂; and

   146 wherein aryl is phenyl or naphthyl; and wherein heteroaryl is a 5- or 6-membered aromatic ring which contains 1, 2 or 3 heteroatoms independently of each other selected from N, O and S, wherein the H-atom in one or more NH groups may be optionally replaced by Rⁿ; and wherein aryl and heteroaryl may be optionally substituted with one or more substituents L^A; and

   R^NT2 is selected from the group R^NT2-G1 consisting of H and C^e-alkyl; or

   R^NT1 and R^ntz are linked to form one group selected from the group R^NT1R^NT2-G1 consisting of a C3-₅-alkylene group, wherein 1 or 2 -CH2-groups independently of each other are replaced by NRⁿ, O, C(=O), S, S(=O) or S(=O)₂; and which may be optionally substituted with one or more substituents independently of each other selected from F, Cw-alkyl, (Rⁿ)₂N, OH and Ci_4-alkyl-O-;

   L^a is selected from the group L^Ar-G1 consisting of F, Cl, Br, CN, OH, NO2, Ci. 4-alkyl-, Cw-alkyl-O-, (Rⁿ)2N-C(=O), (Rⁿ)₂N-, and C_M-alkyl-S(=O)₂-, wherein each alkyl group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN, OH and C-i-3-alkyl-O-; and

   L^p is selected from the group L^p-G1 consisting of F and C₁₃-alkyl, wherein the alkyl group may be substituted with one or more F-atoms; and

   L^q is selected from the group L°-G1 consisting of F and Ci-3-alkyl, wherein the alkyl group may be substituted with one or more F-atoms; and vy/

   147

   R^c is selected from the group R^c-G1 consisting of F, Cl, Br, I, CN, OH, NO21 Ci-6-alkyl-, Ci-6-alkenyl-, C-i-e-alkynyl-, C3-6-cycloalkyl, Ci.6-alkyl-O-, C3-ecycloalkyl-O-, C-|.6-alkyl-S-, HO-C(=O)-, Cv6-alkyl-O-C(=O)-, Ci-4-alkylC(=O)-, C3.6-cycloalkyl-C(=0)-, Ci^-alkyl-S(=O)-, CM-alkyl-S(=O)2-, R^NT1R^NT2N-, R^NT1R^NT2N-C(=O)-, R^nt1R^NT2N-S(=O)2-, R^nt1R^NT2N-C(=O)(Rⁿ)N-, heterocyclyl, heterocyclyl-O-, aryl, aryl-O-, heteroaryl and heteroaryl-O-, wherein each alkyl, alkenyl, alkynyl, and cycloalkyl group may be optionally substituted with one or more substituents independently of each other selected from F, Cl, CN, OH, Cv3-alkyl, C3.6-cycloalkyl, C1.3alkyl-O-, R^NT1R^NT2N-, R^nt1R^NT2N-C(=O)-, Ci.4-alkyl-S(=O)-, Ci.₄-alkylS(=O)₂-, R^NT1R^NT2N-S(=O)₂-, aryl, heteroaryl, and heterocyclyl, and wherein aryl dénotés phenyl or naphthyl, and wherein heteroaryl is a 5- or 6-membered aromatic ring which contains 1, 2, 3 or 4 heteroatoms independently of each other selected from N, O and S, wherein the H-atom in one or more NH groups may be optionally replaced by R^N; and wherein heterocyclyl is a 4- to 7-membered unsaturated or saturated carbocyclic ring in which 1 or 2 -CH₂-groups independently of each other are replaced by NRⁿ, O, -C(=O)-, S, -S(=O)- or -S(=O)₂-, and/or in which a -CH-group is replaced by N; and wherein each aryl, heteroaryl or heterocyclyl group may be optionally substituted with one or more substituents independently of each other selected from L^A; and

   X¹, X², X³ are independently selected from the group X-G1 consisting of C(R²) and N, such that 0, 1 or 2 members of the group consisting of X¹, X², and X³ hâve the meaning N; and .k/

   148

   R² is selected from the group R²-G1 consisting of H, F, Cl, CN, OH, Cmalkyl, C3-7-cycloalkyl-, F₂HC, F₃C, C-M-alkyl-O-, F₂HC-O-, F₃C-O- and C₃.₇cycloalkyl-O-; and n is an integer selected from 0, 1,2, 3 or 4; and m is an integer selected from 0,1, or 2;

   or a sait thereof.
2. 2. A compound according to claim 1 wherein R¹ is selected from a group consisting of a 5-membered heteroaromatic ring which contains 2 or 3 heteroatoms independently of each other selected from N, O and S and a 6membered heteroaromatic ring which contains 1 or 2 N atoms; and wherein optionally a second ring may be condensed to said 5- and 6-membered heteroaromatic rings, wherein said second ring is unsaturated or aromatic and 5or 6-membered and may contain 1 or 2 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH2-groups may be optionally replaced by -N(Rⁿ)-, -C(=O)- or-S(=O)2-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more NH groups may be optionally replaced by R^N, and wherein each of said heteroaromatic ring and/or second ring independently of each other may be optionally substituted with one or two substituents selected from L^a; and wherein said heteroaromatic ring or said second ring may be optionally substituted with a group R^c; wherein R^N, L^A and R^c are defined as in claim 1.
3. 3. A compound according to claim 1 or 2 wherein A is selected from a group consisting of a phenyl ring, a 6-membered heteroaromatic ring which contains 1 or 2 N-atoms and a 5-membered heteroaromatic ring which contains 1,

   149

   2 or 3 heteroatoms independently of each other selected from N, O and S; wherein said phenyl ring or heteroaromatic ring is substituted with a group T, and wherein said phenyl ring and heteroaromatic ring may be optionally substituted with one or more substituents independently of each other selected from L^A, wherein in said heteroaromatic rings the H-atom in one or more NH groups may be optionally replaced by R^N, wherein T, R^N and L^A are defined as in claim 1.
4. 4. A compound according to claim 1 or 2 wherein A is selected from a group consisting of a phenyl ring and a 5- or 6-membered heteroaromatic ring which contains 1or 2 heteroatoms independently of each other selected from N, O or S; and wherein a second ring is condensed to said phenyl ring or said heteroaromatic ring, wherein said second ring is unsaturated or aromatic and is 5or 6-membered and may optionally contain 1 or 2 heteroatoms independently of each other selected from N, O and S, and wherein in said second ring 1 or 2 -CH₂-groups may be optionally replaced by -N(Rⁿ)-, -0(=0)-, -S(=O)- or -S(=O)₂-, and wherein in said heteroaromatic ring and/or said second ring the H-atom in one or more N H groups may be optionally replaced by R^N, and wherein each of said phenyl ring, heteroaromatic ring and second ring may be optionally substituted with one or more substituents independently of each other selected from L^A; and wherein said phenyl ring, heteroaromatic ring or second ring may be optionally substituted with a group T; and wherein R^N, T and L^A are defined as in claim 1.

   150
5. 5. A compound according to claim 1 or 2 wherein A is selected from a group consisting of 1,2,3,6-tetrahydropyridin-4-yl wherein the H of the NH group is replaced by Ci.₄-alkyl-S(=O)2-.
6. 6. A compound according to claim 1,2, 3, 4 or 5 wherein T is selected from a group consisting of CN, C-₁^-alkyl-S(=O)₂-CH₂ -, C₁.₄-alkyl-S(=O)2, R^NT1R^NT2N-S(=O)2-, R^NT1R^NT2N-C(=O)-, C1.₄-alkyl-S(⁼O)₂-(R^)N-, and R^NT1R^NT2N-, wherein R^NT1, R^NT2, and R^N are defined as in claim 1.
7. 7. A compound according to claim 1, wherein

   X¹ is CH;

   X² is CH or N;

   X³ is CH;

   R¹ is selected from the group R¹-G4a consisting of:

   wherein each ring may be optionally substituted with one substituent R^c;

   R^c is selected from the group R^c-G4b consisting of F, Cl, Ci.₄-alkyl, F3C- and cyclopropyl, wherein the cyclopropyl group may be monosubstituted with CH3;

   A is selected from the group A-G6a consisting of:

   F

   151

   10 L^Q is CH₃;

   152 m is 0 or 1;

   and the pharmaceutically acceptable salts thereof.
8. 8. A compound according to claim 7, wherein

   X¹ is CH;

   X² is N;

   X³ is CH;

   R¹ is selected from the group consisting of:

   wherein each ring may be optionally substituted with one F and/or with one substituent R^c;

   R^c is selected from the group consisting of F, Cl, Ci-4-alkyl, F₃C- and cyclopropyl, wherein the cyclopropyl group may be monosubstituted with CH₃;

   A is selected from the group consisting of:

   L° is CH₃;

   n is 0;

   m is 0 or 1;

   and the pharmaceutically acceptable salts thereof.

   153
9. 9.

   9. A pharmaceutically acceptable sait of a compound according to one or more of the ciaims 1 to 8.
10. 10.

    A pharmaceutical composition comprising one or more compounds according to one or more of the ciaims 1 to 8 or one or more pharmaceutically acceptable salts thereof, optionally together with one or more inert carriers and/or diluents.
11. 11. Use of a compound according to one or more of the ciaims 1 to 8 or a pharmaceutically acceptable sait thereof in the manufacture of a médicament useful for treating diseases or conditions which are mediated by activating the Gprotein-coupled receptor GPR119.
12. 12. A compound according to any one of ciaims 1 to 8 or a pharmaceutically acceptable sait thereof for use in a method of treating diabètes, obesity or dyslipidemia.
13. 13. A pharmaceutical composition comprising one or more compounds according to one or more of the ciaims 1 to 8 or one or more pharmaceutically acceptable salts thereof and one or more additional therapeutic agents, optionally together with one or more inert carriers and/or diluents