ES2625256T3 - Compuestos de tetrahidroisoquinolina sustituidos como inhibidores del factor XIA - Google Patents
Compuestos de tetrahidroisoquinolina sustituidos como inhibidores del factor XIA Download PDFInfo
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- ES2625256T3 ES2625256T3 ES12778913T ES12778913T ES2625256T3 ES 2625256 T3 ES2625256 T3 ES 2625256T3 ES 12778913 T ES12778913 T ES 12778913T ES 12778913 T ES12778913 T ES 12778913T ES 2625256 T3 ES2625256 T3 ES 2625256T3
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- 239000003112 inhibitor Substances 0.000 title 1
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 70
- 125000005843 halogen group Chemical group 0.000 abstract 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 7
- 125000002947 alkylene group Chemical group 0.000 abstract 7
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- -1 -CH2NH2- Chemical group 0.000 abstract 2
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 2
- 125000003003 spiro group Chemical group 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 1
- 101100134927 Gallus gallus COR8 gene Proteins 0.000 abstract 1
- 108010081348 HRT1 protein Hairy Proteins 0.000 abstract 1
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005275 alkylenearyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
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- C07D487/02—Heterocyclic 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
- C07D487/08—Bridged systems
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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Abstract
Un compuesto de acuerdo con la fórmula (I):**Fórmula** o un estereoisómero, un tautómero, una sal farmacéuticamente aceptable o un solvato del mismo, en la que: el anillo A es un carbociclo C3-6; el anillo B es un heterociclo de 4 a 7 miembros que contiene átomos de carbono y 0-3 heteroátomos adicionales seleccionados entre el grupo que consiste en N, NR6, O y S(O)p; opcionalmente, el anillo B forma un anillo condensado o un anillo espiro con un heterociclo de 4 a 7 miembros que contiene átomos de carbono y 1-3 heteroátomos seleccionados entre el grupo que consiste en NR6, O y S(O)p; el anillo B, incluyendo el anillo condensado o el anillo espiro, está sustituido con 1-3 R5; L se selecciona entre el grupo que consiste en: -CHR10CHR10-, -CR10>=CR10-, -CºC-, -CHR10NH-, -NHCHR10-, - SCH2-, -CH2S-, -SO2CH2-, -CH2SO2-, -NHCH2- y -CH2NH-; R1, en cada aparición, se selecciona entre el grupo que consiste en: H, halo, alquilo C1-6, alcoxi C1-4, alquiltio C1-4, OH, SH, CHF2, CF3, OCF3, CN, NH2, CO-alquilo C1-4, CO2(alquilo C1-4), -CH2CO2H, -CH2CO2(alquilo C1-4), - CH2NH2, -CONH2, -CONH(alquilo C1-4), -NHCO(alquilo C1-4), -NHCO2(alquilo C1-4), -NHSO2(alquilo C1-4) y - SO2NH2 y -C(>=NH)NH2; R2 se selecciona entre el grupo que consiste en: H, halo, CN, OH, alquilo C1-6, alcoxi C1-4, haloalquilo C1-6, haloalcoxi C1-6, CO(alquilo C1-4), CONH2, CO2H, CH2NH2 y un heterociclo de 5 a 7 miembros que comprende átomos de carbono y 1-4 heteroátomos seleccionados entre N, NRc, O y S(O)p, en donde dicho heterociclo está sustituido con 0-2 R2a; R2a, en cada aparición, se selecciona entre el grupo que consiste en: H, halo, alquilo C1-4, alcoxi C1-4, OH, CF3, OCF3, CN, NH2, CO2H, CO2(alquilo C1-4), CO(alquilo C1-4), -CONH2, -CH2OH, -CH2O-alquilo C1-4, -CH2NH2-, CONH(alquilo C1-4), -CON(alquilo C1-4)2, -SO2(alquilo C1-4), -SO2NH2, -SO2NH(alquilo C1-4) y -SO2N(alquilo C1-4)2; R3 se selecciona entre el grupo que consiste en: alquilo C1-6 sustituido con 1-3 R3a, -(CH2)n-carbociclo C3-10 sustituido con 0-3 R3a o -(CH2)n-heterociclo de 5-10 miembros que contiene átomos de carbono y 1-4 heteroátomos seleccionados entre el grupo que consiste en N, NR7, O y S(O)p; en donde dicho heterociclo está sustituido con 0-3 R3a; R3a, en cada aparición, se selecciona entre el grupo que consiste en: >=O, halo, alquilo C1-4, OH, alcoxi C1-4, CN, NH2, CO2H, CO2(alquilo C1-4), CONH2, CONH(alquilo C1-6), CON(alquilo C1-4)2, -CONH-alquilen C1-4-CO2(alquilo C1-4), -CONHCO2-alquilo C1-4, -CONH-alquilen C1-4-NHCO(alquilo C1-4), -CONH-alquilen C1-4-CONH2, -NHCO alquilo C1-4, -NHCO2(alquilo C1-4), -alquilen C1-4-NHCO2-alquilo C1-4, Rf, CONHRf y -CO2Rf; R4, en cada aparición, se selecciona entre el grupo que consiste en: H, halo y alquilo C1-4; R5, en cada aparición, se selecciona entre el grupo que consiste en: H, >=O, halo, alquilo C1-4, OH, CN, NH2, - N(alquilo C1-4)2, NO2, alcoxi C1-4, -OCO(alquilo C1-4), -O-alquilen C1-4-O(alquilo C1-4), -O-alquilen C1-4-N(alquilo C1- 4)2, -CO2H, -CO2(alquilo C1-4), -CONH2, -(CH2)2CONH2, -CONR9(alquilo C1-4), -CONR9-alquilen C1-4-O(alquilo C1- 4), -CON(alquilo C1-4)2, -CONR9-alquilen C1-4-N(alquilo C1-4)2, -CON(alquil C1-4)-alquilen C1-4-O(alquilo C1-4), - CONR9-alquilen C1-4-CO2(alquilo C1-4), -NR9CO-alquilo C1-4, -NR9CO2-alquilo C1-4, -NR9CONH(alquilo C1-4), - NR9CONR9-alquilen C1-4-CO2-alquilo C1-4, -NR9-alquilen C1-4-N(alquilo C1-4)2, R8, -OR8, -O-alquilen C1-4-R8, - COR8, -CO2R8, -CONR9R8, -NR9COR8, -NR9CO2R8 y -NR9CON R9R8; R6 se selecciona entre el grupo que consiste en: H, alquilo C1-4, -CO2(alquilo C1-4), -CO(alquilo C1-4), -CONH2, - CO-alquilen C1-4-N(alquilo C1-4)2, -(CH2)2N(alquilo C1-4)2, -CONR9(alquilo C1-4), -CONR9-alquilen C1-4-O(alquilo C1- 4), -CONR9-alquilen C1-4-N(alquilo C1-4)2, -CONR9-alquilen C1-4-CO2(alquilo C1-4), -CON(alquilo C1-4)2, R8, -COR8, - CO2R8 y -CONR9R8; R7, en cada aparición, se selecciona entre el grupo que consiste en: H, alquilo C1-4, CO-alquilo C1-4, CO2(alquilo C1-4), CO2Bn, -CONH-alquilen C1-4-CO2-alquilo C1-4, fenilo, bencilo y -CO2-alquilen C1-4-arilo; R8, en cada aparición, se selecciona entre el grupo que consiste en: -(CH2)n-carbociclo C3-10 sustituido con 0-3 Re y -(CH2)n-heterociclo de 5-10 miembros que contiene átomos de carbono y 1-4 heteroátomos seleccionados entre el grupo que consiste en N, NRd, O y S(O)p; en donde dichos carbociclo y heterociclo están opcionalmente sustituidos con >=O; R9, en cada aparición, se selecciona entre el grupo que consiste en: H y alquilo C1-4; R10, en cada aparición, se selecciona entre el grupo que consiste en: H, halo, OH y alquilo C1-4; Rc se selecciona, independientemente en cada aparición, entre el grupo que consiste en: H, alquilo C1-4, COalquilo C1-4, CO2-alquilo C1-4 y CO2Bn; Rd se selecciona, independientemente en cada aparición, entre el grupo que consiste en: H, alquilo C1-4, CO(alquilo C1-4), COCF3, CO2(alquilo C1-4), -CONH-alquilen C1-4-CO2-alquilo C1-4, CO2Bn, Rf y CONHRf; Re se selecciona, independientemente en cada aparición, entre el grupo que consiste en: >=O, halo, alquilo C1-4, alcoxi C1-4, OCF3, NH2, NO2, N(alquilo C1-4)2, CO(alquilo C1-4), CO(haloalquilo C1-4), CO2(alquilo C1-4), CONH2, - CONH(alquilo C1-4), -CONHPh, -CON(alquilo C1-4)2, -CONH-alquilen C1-4-O(alquilo C1-4), -CONH-alquilen C1-4- N(alquilo C1-4)2, -CONH-alquilen C1-4-CO2(alquilo C1-4), -NHCO2(alquilo C1-4), Rf, CORf, CO2Rf y CONHRf; Rf se selecciona, independientemente en cada aparición, entre el grupo que consiste en: -(CH2)n-cicloalquilo C3-6, -(CH2)n-fenilo y -(CH2)n-heterociclo de 5 a 6 miembros que contiene átomos de carbono y 1-4 heteroátomos seleccionados entre el grupo que consiste en N, NRc, O y S(O)p; en donde cada resto del anillo está sustituido con 0-2 Rg; Rg se selecciona, independientemente en cada aparición, entre el grupo que consiste en: >=O, halo, alquilo C1-4, OH, alcoxi C1-4 y NHCO(alquilo C1-4); n, en cada aparición, se selecciona entre 0, 1, 2, 3 y 4; y p, en cada aparición, se selecciona entre 0, 1 y 2.
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| PCT/US2012/059969 WO2013056060A1 (en) | 2011-10-14 | 2012-10-12 | Substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
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