ES2566387T3 - Compuestos heterocíclicos condensados de pirid-2-ilo, y composiciones y usos de los mismos - Google Patents
Compuestos heterocíclicos condensados de pirid-2-ilo, y composiciones y usos de los mismos Download PDFInfo
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- ES2566387T3 ES2566387T3 ES08727238.1T ES08727238T ES2566387T3 ES 2566387 T3 ES2566387 T3 ES 2566387T3 ES 08727238 T ES08727238 T ES 08727238T ES 2566387 T3 ES2566387 T3 ES 2566387T3
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- Prior art keywords
- substituted
- pyridin
- unsubstituted
- compound according
- compound
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- 239000000203 mixture Substances 0.000 title claims description 114
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 title description 10
- 150000002391 heterocyclic compounds Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 265
- -1 azido, carbamoyl Chemical group 0.000 claims abstract description 141
- 125000003118 aryl group Chemical group 0.000 claims abstract description 75
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 67
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 58
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 52
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 38
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 31
- 150000003839 salts Chemical class 0.000 claims abstract description 23
- 125000002252 acyl group Chemical group 0.000 claims abstract description 21
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 21
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims abstract description 21
- 239000012453 solvate Substances 0.000 claims abstract description 20
- 125000004442 acylamino group Chemical group 0.000 claims abstract description 19
- 125000004404 heteroalkyl group Chemical group 0.000 claims abstract description 19
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 18
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 18
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 17
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims abstract description 14
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 11
- 125000003396 thiol group Chemical group [H]S* 0.000 claims abstract description 11
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 10
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- 125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 7
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- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims description 7
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- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 claims description 5
- 108010081348 HRT1 protein Hairy Proteins 0.000 claims description 5
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- 231100000869 headache Toxicity 0.000 claims description 5
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 5
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- 125000004076 pyridyl group Chemical group 0.000 claims description 5
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- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 5
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
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- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 4
- 230000002485 urinary effect Effects 0.000 claims description 4
- COHPLRFPNJNJIX-GOSISDBHSA-N (2s)-2-(6-methoxypyridin-3-yl)-2-[[6-(5-methylpyridin-2-yl)-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-yl]amino]ethanol Chemical compound C1=NC(OC)=CC=C1[C@@H](CO)NC1=NC=NC2=C1CN(C=1N=CC(C)=CC=1)CC2 COHPLRFPNJNJIX-GOSISDBHSA-N 0.000 claims description 3
- WPBBTBJCOJRQNE-QGZVFWFLSA-N (2s)-2-[[6-(5-chloropyridin-2-yl)-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-yl]amino]-2-(6-methoxypyridin-3-yl)ethanol Chemical compound C1=NC(OC)=CC=C1[C@@H](CO)NC1=NC=NC2=C1CN(C=1N=CC(Cl)=CC=1)CC2 WPBBTBJCOJRQNE-QGZVFWFLSA-N 0.000 claims description 3
- PUIPLPMBTAVSBG-GOSISDBHSA-N (3r)-3-(6-methoxypyridin-3-yl)-3-[[6-(5-methylpyridin-2-yl)-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-yl]amino]propan-1-ol Chemical compound C1=NC(OC)=CC=C1[C@@H](CCO)NC1=NC=NC2=C1CN(C=1N=CC(C)=CC=1)CC2 PUIPLPMBTAVSBG-GOSISDBHSA-N 0.000 claims description 3
- XNAFMMCWOUXFDU-CQSZACIVSA-N 6-(5-methylpyridin-2-yl)-n-[(1r)-1-(2-methylpyrimidin-5-yl)ethyl]-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-amine Chemical compound N([C@H](C)C=1C=NC(C)=NC=1)C(C=1C2)=NC=NC=1CCN2C1=CC=C(C)C=N1 XNAFMMCWOUXFDU-CQSZACIVSA-N 0.000 claims description 3
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 3
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- 208000034347 Faecal incontinence Diseases 0.000 claims description 3
- 208000014540 Functional gastrointestinal disease Diseases 0.000 claims description 3
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- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 3
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- 206010039085 Rhinitis allergic Diseases 0.000 claims description 3
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- 210000000481 breast Anatomy 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 230000003001 depressive effect Effects 0.000 claims description 3
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 3
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
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- 125000002757 morpholinyl group Chemical group 0.000 claims description 3
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- SSNDZSZPTDFBHC-LJQANCHMSA-N (3r)-3-(6-methylpyridin-3-yl)-3-[[6-(5-methylpyridin-2-yl)-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-yl]amino]propan-1-ol Chemical compound N1=CC(C)=CC=C1N1CC2=C(N[C@H](CCO)C=3C=NC(C)=CC=3)N=CN=C2CC1 SSNDZSZPTDFBHC-LJQANCHMSA-N 0.000 claims description 2
- SGUGDZUWFAUPNY-QGZVFWFLSA-N (3r)-3-[[6-(5-chloropyridin-2-yl)-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-yl]amino]-3-(6-methoxypyridin-3-yl)propan-1-ol Chemical compound C1=NC(OC)=CC=C1[C@@H](CCO)NC1=NC=NC2=C1CN(C=1N=CC(Cl)=CC=1)CC2 SGUGDZUWFAUPNY-QGZVFWFLSA-N 0.000 claims description 2
- JYXGOVPRQNIYKV-QGZVFWFLSA-N (3r)-3-[[6-(5-methylpyridin-2-yl)-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-yl]amino]-3-[6-(trifluoromethyl)pyridin-3-yl]propan-1-ol Chemical compound N1=CC(C)=CC=C1N1CC2=C(N[C@H](CCO)C=3C=NC(=CC=3)C(F)(F)F)N=CN=C2CC1 JYXGOVPRQNIYKV-QGZVFWFLSA-N 0.000 claims description 2
- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- VCVJHUNWPOOPQN-GFCCVEGCSA-N 6-(5-chloropyridin-2-yl)-n-[(1r)-1-[6-(trifluoromethyl)pyridin-3-yl]ethyl]-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-amine Chemical compound N([C@H](C)C=1C=NC(=CC=1)C(F)(F)F)C(C=1C2)=NC=NC=1CCN2C1=CC=C(Cl)C=N1 VCVJHUNWPOOPQN-GFCCVEGCSA-N 0.000 claims description 2
- ICLOKAIXSUXTKZ-CQSZACIVSA-N 6-(5-methylpyridin-2-yl)-n-[(1r)-1-[6-(trifluoromethyl)pyridin-3-yl]ethyl]-7,8-dihydro-5h-pyrido[4,3-d]pyrimidin-4-amine Chemical compound N([C@H](C)C=1C=NC(=CC=1)C(F)(F)F)C(C=1C2)=NC=NC=1CCN2C1=CC=C(C)C=N1 ICLOKAIXSUXTKZ-CQSZACIVSA-N 0.000 claims description 2
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- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 2
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- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
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Landscapes
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92160407P | 2007-04-02 | 2007-04-02 | |
| US92160307P | 2007-04-02 | 2007-04-02 | |
| US921603P | 2007-04-02 | ||
| US921604P | 2007-04-02 | ||
| PCT/US2008/004202 WO2008123963A1 (en) | 2007-04-02 | 2008-03-31 | Pyrid-2-yl fused heterocyclic compounds, and compositions and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2566387T3 true ES2566387T3 (es) | 2016-04-12 |
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| ES (1) | ES2566387T3 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2008123963A1 (cg-RX-API-DMAC7.html) |
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| PT2139334E (pt) * | 2007-04-17 | 2013-10-02 | Evotec Ag | Compostos heterocíclicos fusionados de 2-cianofenilo, e composições e utilizações dos mesmos |
| WO2010080503A1 (en) * | 2008-12-19 | 2010-07-15 | Genentech, Inc. | Heterocyclic compounds and methods of use |
| UA112517C2 (uk) * | 2010-07-06 | 2016-09-26 | Новартіс Аг | Тетрагідропіридопіримідинові похідні |
| EP2619204A4 (en) * | 2010-09-21 | 2014-08-27 | Merck Sharp & Dohme | TRIAZOLOPYRAZINONE AS P2X7 RECEPTOR ANTAGONISTS |
| AU2012354094C1 (en) | 2011-12-15 | 2015-10-15 | Novartis Ag | Use of inhibitors of the activity or function of PI3K |
| JP6458429B2 (ja) * | 2014-09-30 | 2019-01-30 | 大日本印刷株式会社 | 導電材充填貫通電極基板及びその製造方法 |
| SI3587417T1 (sl) | 2014-12-09 | 2022-04-29 | Bayer Ag | 1,3-tiazol-2-il substituirani benzamidi |
| US10183937B2 (en) | 2014-12-09 | 2019-01-22 | Bayer Aktiengesellschaft | 1,3-thiazol-2-yl substituted benzamides |
| CN108368127B (zh) * | 2015-07-23 | 2020-12-11 | 武田药品工业株式会社 | 化合物及其作为ep4受体拮抗剂的用途 |
| US20230096028A1 (en) * | 2019-03-01 | 2023-03-30 | Revolution Medicines, Inc. | Bicyclic heterocyclyl compounds and uses thereof |
| MX2021014116A (es) | 2019-05-31 | 2021-12-10 | Chiesi Farm Spa | Derivados de piridopirimidinas como inhibidores del purinoreceptor 3 de p2x (p2x3). |
| MA56021A (fr) | 2019-05-31 | 2022-04-06 | Chiesi Farm Spa | Dérivés d'amino quinazoline servant d'inhibiteurs de p2x3 |
| WO2022028506A1 (zh) * | 2020-08-06 | 2022-02-10 | 北京泰德制药股份有限公司 | Sos1抑制剂、包含其的药物组合物及其用途 |
| JP2023550830A (ja) * | 2020-11-27 | 2023-12-05 | キエシ・フアルマチエウテイチ・ソチエタ・ペル・アチオニ | Ｐ２ｘ３阻害剤としての（アザ）キノリン４－アミン誘導体 |
| JP2023550840A (ja) * | 2020-11-27 | 2023-12-05 | キエシ・フアルマチエウテイチ・ソチエタ・ペル・アチオニ | Ｐ２ｘ３阻害剤としてのアミノキナゾリン誘導体 |
| JP2023550831A (ja) * | 2020-11-27 | 2023-12-05 | キエシ・フアルマチエウテイチ・ソチエタ・ペル・アチオニ | Ｐ２ｘ３阻害剤としてのフタラジン誘導体 |
| AU2022217353B2 (en) * | 2021-02-08 | 2025-01-09 | Wuhan Humanwell Innovative Drug Research and Development Center Limited Company | Pyridopyrimidinone derivative, preparation method therefor, and use thereof |
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| US3424760A (en) | 1966-03-07 | 1969-01-28 | Robins Co Inc A H | 3-ureidopyrrolidines |
| US3424761A (en) | 1966-03-07 | 1969-01-28 | Robins Co Inc A H | 3-ureidopyrrolidines |
| DE2502588A1 (de) | 1975-01-23 | 1976-07-29 | Troponwerke Dinklage & Co | Basisch substituierte derivate des 7-amino-2-chinolons, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| JP2001526222A (ja) | 1997-12-22 | 2001-12-18 | バイエル コーポレイション | アリールおよびヘテロアリール置換複素環尿素を使用するｐ３８キナーゼ活性の阻害 |
| KR100622138B1 (ko) | 1997-12-22 | 2006-09-13 | 바이엘 코포레이션 | 아릴 및 헤테로아릴 치환 헤테로고리형 우레아를 사용한라프 키나제의 저해 |
| AU778393B2 (en) | 1999-05-12 | 2004-12-02 | Ortho-Mcneil Pharmaceutical, Inc. | Pyrazole carboxamides useful for the treatment of obesity and other disorders |
| WO2001051490A1 (en) * | 2000-01-14 | 2001-07-19 | The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Methanocarba cycloalkyl nucleoside analogues |
| US6531478B2 (en) | 2000-02-24 | 2003-03-11 | Cheryl P. Kordik | Amino pyrazole derivatives useful for the treatment of obesity and other disorders |
| CA2415606A1 (en) | 2000-07-20 | 2002-01-31 | Neurogen Corporation | Capsaicin receptor ligands |
| WO2002053558A1 (en) | 2001-01-02 | 2002-07-11 | F.Hoffman-La Roche Ag | Quinazolone derivatives as alpha 1a/b adrenergic receptor antagonists |
| WO2002088079A2 (en) | 2001-05-01 | 2002-11-07 | Bristol-Myers Squibb Company | Dual inhibitors of pde 7 and pde 4 |
| WO2003072569A1 (en) | 2002-02-25 | 2003-09-04 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1,4-disubstituted benzofused cycloalkyl urea compounds useful in treating cytokine mediated diseases |
| GB0206033D0 (en) | 2002-03-14 | 2002-04-24 | Pfizer Ltd | Compounds useful in therapy |
| EP1552842A1 (en) * | 2002-06-07 | 2005-07-13 | Kyowa Hakko Kogyo Co., Ltd. | Bicyclic pyrimidine derivatives |
| GB0225908D0 (en) | 2002-11-06 | 2002-12-11 | Pfizer Ltd | Treatment of female sexual dysfunction |
| CA2510471A1 (en) | 2002-12-19 | 2004-07-08 | Neurogen Corporation | Substituted biphenyl-4-carboxylic acid arylamide analogues as capsaicin receptor modulators |
| CN101010315A (zh) | 2004-04-30 | 2007-08-01 | 拜耳制药公司 | 用于治疗癌症的取代的吡唑基脲衍生物 |
| WO2006119504A2 (en) * | 2005-05-04 | 2006-11-09 | Renovis, Inc. | Fused heterocyclic compounds, and compositions and uses thereof |
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- 2008-03-31 EP EP08727238.1A patent/EP2136639B1/en not_active Not-in-force
- 2008-03-31 JP JP2010502114A patent/JP5396379B2/ja not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2010523562A (ja) | 2010-07-15 |
| EP2136639A4 (en) | 2011-11-02 |
| JP5396379B2 (ja) | 2014-01-22 |
| US8653091B2 (en) | 2014-02-18 |
| EP2136639B1 (en) | 2016-03-09 |
| EP2136639A1 (en) | 2009-12-30 |
| CA2682162C (en) | 2016-05-10 |
| US20110009432A1 (en) | 2011-01-13 |
| WO2008123963A1 (en) | 2008-10-16 |
| HK1140106A1 (zh) | 2010-10-08 |
| CA2682162A1 (en) | 2008-10-16 |
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