WO2009038021A1 - 4-スルホニルピペリジン誘導体 - Google Patents

4-スルホニルピペリジン誘導体 Download PDF

Info

Publication number
WO2009038021A1
WO2009038021A1 PCT/JP2008/066525 JP2008066525W WO2009038021A1 WO 2009038021 A1 WO2009038021 A1 WO 2009038021A1 JP 2008066525 W JP2008066525 W JP 2008066525W WO 2009038021 A1 WO2009038021 A1 WO 2009038021A1
Authority
WO
WIPO (PCT)
Prior art keywords
diseases
alkyl
forms
sulfonylpiperidine
derivatives
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2008/066525
Other languages
English (en)
French (fr)
Inventor
Tsuyoshi Nagase
Takahide Sasaki
Toshiyuki Takahashi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MSD KK
Original Assignee
Banyu Phamaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Banyu Phamaceutical Co Ltd filed Critical Banyu Phamaceutical Co Ltd
Priority to JP2009533122A priority Critical patent/JP5319536B2/ja
Priority to AU2008301718A priority patent/AU2008301718B2/en
Priority to EP08831915.7A priority patent/EP2204368B1/en
Priority to CA2699275A priority patent/CA2699275C/en
Priority to US12/674,999 priority patent/US8163898B2/en
Publication of WO2009038021A1 publication Critical patent/WO2009038021A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

【課題】 循環器系疾患、神経系疾患、代謝性疾患、生殖系疾患、消化管系疾患の予防剤又は治療剤として有用な化合物を提供する。 【解決手段】 式(I) [式中、R1は、C1-6アルキル基、C3-8シクロアルキル基等を表し、R2は、フェニル基又はヘテロアリール基等を表し、Qは、N又はCHを表し、M1、M2、M3及びM4は、それぞれ独立して、水素原子若しくはC1-6アルキル基を表すか、又は、M1は、M2又はM3と一緒になって、-CH2-CH2-等を形成するか、若しくはM4は、M2又はM3と一緒になって、-CH2-CH2-等を形成し、但し、M1、M2、M3及びM4は、それらのなかで1つの-CH2-又は-CH2-CH2-を形成するものとする]で表される化合物又は薬学的に許容されるその塩。
PCT/JP2008/066525 2007-09-21 2008-09-12 4-スルホニルピペリジン誘導体 Ceased WO2009038021A1 (ja)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP2009533122A JP5319536B2 (ja) 2007-09-21 2008-09-12 4−スルホニルピペリジン誘導体
AU2008301718A AU2008301718B2 (en) 2007-09-21 2008-09-12 4-sulfonylpiperidine derivatives
EP08831915.7A EP2204368B1 (en) 2007-09-21 2008-09-12 4-sulfonylpiperidine derivatives
CA2699275A CA2699275C (en) 2007-09-21 2008-09-12 4-sulfonylpiperidine derivative
US12/674,999 US8163898B2 (en) 2007-09-21 2008-09-12 4-sulfonylpiperidine derivatives

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007244731 2007-09-21
JP2007-244731 2007-09-21

Publications (1)

Publication Number Publication Date
WO2009038021A1 true WO2009038021A1 (ja) 2009-03-26

Family

ID=40467837

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/066525 Ceased WO2009038021A1 (ja) 2007-09-21 2008-09-12 4-スルホニルピペリジン誘導体

Country Status (6)

Country Link
US (1) US8163898B2 (ja)
EP (1) EP2204368B1 (ja)
JP (1) JP5319536B2 (ja)
AU (1) AU2008301718B2 (ja)
CA (1) CA2699275C (ja)
WO (1) WO2009038021A1 (ja)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8314094B2 (en) 2007-10-05 2012-11-20 Msd K.K Benzoxazinone derivative
JP5377329B2 (ja) * 2007-12-26 2013-12-25 Msd株式会社 スルホニル置換六員環誘導体

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004024720A1 (en) * 2002-09-11 2004-03-25 Merck & Co., Inc. Piperazine urea derivatives as melanocortin-4 receptor agonists
WO2005005665A1 (ja) 2003-07-11 2005-01-20 Banyu Pharmaceutical Co., Ltd. Lceによる肥満治療に有効な化合物の評価方法
WO2007007069A1 (en) * 2005-07-07 2007-01-18 Vernalis (R & D) Limited Azacyclic compounds as inhibitors of sensory neurone specific sodium channels

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK77498A3 (en) * 1995-12-14 1999-01-11 Merck & Co Inc Nonpeptide derivatives, pharmaceutical composition containing them and their use
FR2744449B1 (fr) * 1996-02-02 1998-04-24 Pf Medicament Nouvelles piperazines aromatiques derivees de cycloazanes substitues, ainsi que leur procede de preparation, les compositions pharmaceutiques et leur utilisation comme medicaments
DE19743435A1 (de) * 1997-10-01 1999-04-08 Merck Patent Gmbh Benzamidinderivate
WO2008026564A1 (en) * 2006-08-30 2008-03-06 Shionogi & Co., Ltd. Urea derivative
CA2682727C (en) * 2007-04-02 2016-03-22 Banyu Pharmaceutical Co., Ltd. Indoledione derivative
US8314094B2 (en) 2007-10-05 2012-11-20 Msd K.K Benzoxazinone derivative
EP2236494B1 (en) 2007-12-26 2016-08-31 Msd K.K. Sulfonyl substituted 6-membered ring derivative
US8188280B2 (en) 2008-02-06 2012-05-29 Msd K.K. 3-substituted sulfonyl piperidine derivative
WO2009131065A1 (ja) 2008-04-24 2009-10-29 萬有製薬株式会社 アリールスルホニル誘導体を有効成分とする長鎖脂肪酸伸長酵素阻害剤

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004024720A1 (en) * 2002-09-11 2004-03-25 Merck & Co., Inc. Piperazine urea derivatives as melanocortin-4 receptor agonists
WO2005005665A1 (ja) 2003-07-11 2005-01-20 Banyu Pharmaceutical Co., Ltd. Lceによる肥満治療に有効な化合物の評価方法
WO2007007069A1 (en) * 2005-07-07 2007-01-18 Vernalis (R & D) Limited Azacyclic compounds as inhibitors of sensory neurone specific sodium channels

Non-Patent Citations (11)

* Cited by examiner, † Cited by third party
Title
"Design of Prodrugs", 1985, ELSEVIER
"The Merck Manual of Medical Information", 2003, MERCK & CO
CELL, vol. 126, 2006, pages 691 - 699
EIJI ITAGAKI: "STEP TaishaINaibunpitsu", 1998, KAIBASHOBO
J. BIOL. CHEM., vol. 276, no. 48, 2001, pages 45358 - 45366
J. LIPID RES., vol. 43, no. 6, 2002, pages 911 - 920
LEE S. H. ET AL., CELL, vol. 126, 2006, pages 691 - 699
MATSUZAKA T. ET AL., J, LIPID RES., vol. 43, no. 6, 2002, pages 911 - 920
MOON, J. BIOL .CHEM., vol. 276, 2001, pages 45358 - 45366
See also references of EP2204368A4
T. W. GREENE: "Protective Groups in Organic Synthesis", 1981, JOHN WILEY & SONS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8314094B2 (en) 2007-10-05 2012-11-20 Msd K.K Benzoxazinone derivative
JP5377329B2 (ja) * 2007-12-26 2013-12-25 Msd株式会社 スルホニル置換六員環誘導体

Also Published As

Publication number Publication date
US8163898B2 (en) 2012-04-24
EP2204368B1 (en) 2014-05-21
EP2204368A1 (en) 2010-07-07
AU2008301718B2 (en) 2013-01-10
US20100234392A1 (en) 2010-09-16
CA2699275A1 (en) 2009-03-26
AU2008301718A1 (en) 2009-03-26
JPWO2009038021A1 (ja) 2011-01-06
CA2699275C (en) 2015-08-25
EP2204368A4 (en) 2012-02-15
JP5319536B2 (ja) 2013-10-16

Similar Documents

Publication Publication Date Title
WO2007117465A3 (en) Indazole compounds
MX2009009492A (es) Compuestos organicos biciclicos adecuados para el tratamiento de condiciones inflamatorias o alergicas.
WO2008062905A3 (en) Heteromonocyclic compound and use thereof
EP2090570A4 (en) IMIDAZOLE DERIVATIVE
WO2007084728A3 (en) 2-imino-benzimidazoles
MX2010009922A (es) Activadores de piridazinona glucocinasa.
AU2008255733A8 (en) Novel 1,2,3,4-tetrahydroquinoxaline derivative which has, as substituent, phenyl group having sulfonic acid ester structure or sulfonic acid amide structure introduced therein and has glucocorticoid receptor-binding activity
MY148703A (en) Polycyclic cinnamide derivatives
NO20084129L (no) Pyridin(3,4-B)Pyrazinoner
TNSN08407A1 (en) Organic compounds
MY172034A (en) Intermediate for producing bicyclic ?-amino acid derivative
NO20073743L (no) Forbindelser med Kv4 ionekanal aktivitet
WO2009044788A1 (ja) ベンゾオキサジノン誘導体
MX2009012125A (es) Compuestos terapeuticos.
WO2012099942A3 (en) Methods and compositions for treating metabolic syndrome
SG155961A1 (en) Pyrazoles as 11-beta-hsd-1
NO20092058L (no) Heteroaryl pyrrolidinyl ketonderivater
MY150507A (en) Polycyclic compound
NO20090064L (no) Pyrasoler som glucokinase aktivatorer
MX2009003081A (es) Derivados de pirrola utiles para el tratamiento de enfermedades mediadas por citoquinas.
WO2008146914A1 (ja) 複素環化合物
WO2012042534A3 (en) Preparation of r-sitagliptin and intermediates thereof
WO2009018065A3 (en) Novel glucokinase activators and methods of using same
BR112013015774A2 (ja) A pyrazole compound which has a curative effect of a multiple myeloma
WO2008141097A9 (en) Stereoisomers propofol therapeutic compounds

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08831915

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2008301718

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2699275

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 2008301718

Country of ref document: AU

Date of ref document: 20080912

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2009533122

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 2008831915

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 12674999

Country of ref document: US