AU2004259765B2 - Thienopyridine and furopyridine kinase inhibitors - Google Patents
Thienopyridine and furopyridine kinase inhibitors Download PDFInfo
- Publication number
- AU2004259765B2 AU2004259765B2 AU2004259765A AU2004259765A AU2004259765B2 AU 2004259765 B2 AU2004259765 B2 AU 2004259765B2 AU 2004259765 A AU2004259765 A AU 2004259765A AU 2004259765 A AU2004259765 A AU 2004259765A AU 2004259765 B2 AU2004259765 B2 AU 2004259765B2
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- Australia
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- aryl
- alkyl
- hydrogen
- amino
- Prior art date
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- YRTCKZIKGWZNCU-UHFFFAOYSA-N furo[3,2-b]pyridine Chemical compound C1=CC=C2OC=CC2=N1 YRTCKZIKGWZNCU-UHFFFAOYSA-N 0.000 title description 2
- 229940043355 kinase inhibitor Drugs 0.000 title description 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title description 2
- DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical compound C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 title 1
- 229940125670 thienopyridine Drugs 0.000 title 1
- 239000002175 thienopyridine Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 235
- 238000000034 method Methods 0.000 claims abstract description 40
- 125000000217 alkyl group Chemical group 0.000 claims description 315
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- 125000001072 heteroaryl group Chemical group 0.000 claims description 194
- -1 alkoxyalkynyl Chemical group 0.000 claims description 140
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 135
- 125000000623 heterocyclic group Chemical group 0.000 claims description 131
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 125
- 125000001424 substituent group Chemical group 0.000 claims description 121
- 125000001188 haloalkyl group Chemical group 0.000 claims description 114
- 125000003545 alkoxy group Chemical group 0.000 claims description 113
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 95
- 125000003342 alkenyl group Chemical group 0.000 claims description 87
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 87
- 125000000304 alkynyl group Chemical group 0.000 claims description 76
- 150000002431 hydrogen Chemical group 0.000 claims description 74
- 229910003827 NRaRb Inorganic materials 0.000 claims description 72
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 72
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- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 64
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 57
- 150000003839 salts Chemical class 0.000 claims description 57
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 43
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 32
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 31
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 claims description 31
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- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 30
- 125000004076 pyridyl group Chemical group 0.000 claims description 29
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- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 21
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 claims description 21
- 239000008194 pharmaceutical composition Substances 0.000 claims description 21
- 125000004449 heterocyclylalkenyl group Chemical group 0.000 claims description 20
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 20
- 125000001544 thienyl group Chemical group 0.000 claims description 18
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- 125000005312 heteroarylalkynyl group Chemical group 0.000 claims description 16
- 125000005016 hydroxyalkynyl group Chemical group 0.000 claims description 16
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 16
- 125000005018 aryl alkenyl group Chemical group 0.000 claims description 15
- 125000005015 aryl alkynyl group Chemical group 0.000 claims description 15
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 15
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 15
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- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims description 10
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 claims description 10
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- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 4
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 4
- 125000005356 cycloalkylalkenyl group Chemical group 0.000 claims description 4
- 125000004447 heteroarylalkenyl group Chemical group 0.000 claims description 4
- 125000004971 nitroalkyl group Chemical group 0.000 claims description 4
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
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- 206010038038 rectal cancer Diseases 0.000 claims description 2
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- 125000001475 halogen functional group Chemical group 0.000 claims 7
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
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- SBXVZMIZJGLIRS-UHFFFAOYSA-N 1-[4-(4-amino-7-pyrimidin-5-ylthieno[3,2-c]pyridin-3-yl)phenyl]-3-(3-methylphenyl)urea Chemical compound CC1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2C3=C(N)N=CC(=C3SC=2)C=2C=NC=NC=2)=C1 SBXVZMIZJGLIRS-UHFFFAOYSA-N 0.000 claims 1
- QJIVDCJIPGAKQZ-UHFFFAOYSA-N 1-[4-[4-amino-7-(2-pyridin-3-ylethynyl)thieno[3,2-c]pyridin-3-yl]phenyl]-3-(3-methylphenyl)urea Chemical compound CC1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2C3=C(N)N=CC(=C3SC=2)C#CC=2C=NC=CC=2)=C1 QJIVDCJIPGAKQZ-UHFFFAOYSA-N 0.000 claims 1
- SEVCBWKJSOLMNQ-UHFFFAOYSA-N 1-[4-[4-amino-7-[3-(diethylamino)prop-1-ynyl]thieno[3,2-c]pyridin-3-yl]phenyl]-3-(3-methylphenyl)urea Chemical compound C=1SC=2C(C#CCN(CC)CC)=CN=C(N)C=2C=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C)=C1 SEVCBWKJSOLMNQ-UHFFFAOYSA-N 0.000 claims 1
- NKEUPUJTVALZIK-UHFFFAOYSA-N 1-[4-[4-amino-7-[3-(methylamino)prop-1-ynyl]thieno[3,2-c]pyridin-3-yl]phenyl]-3-(3-methylphenyl)urea Chemical compound C=1SC=2C(C#CCNC)=CN=C(N)C=2C=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C)=C1 NKEUPUJTVALZIK-UHFFFAOYSA-N 0.000 claims 1
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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
- C07D491/04—Ortho-condensed systems
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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| US20060281768A1 (en) * | 2005-06-10 | 2006-12-14 | Gaul Michael D | Thienopyrimidine and thienopyridine kinase modulators |
| US7566721B2 (en) * | 2005-08-08 | 2009-07-28 | Osi Pharmaceuticals, Inc. | Substituted thienol[2,3-d]pyrimidines as kinase inhibitors |
| BRPI0520482A2 (pt) * | 2005-08-16 | 2009-05-12 | Hoffmann La Roche | amidas do ácido 4-amino-tieno [3,2-c] piridina-7-carboxìlico |
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| JP2009514899A (ja) * | 2005-11-04 | 2009-04-09 | スミスクライン ビーチャム コーポレーション | チエノピリジンＢ−Ｒａｆキナーゼ阻害剤 |
| EP1968979A2 (en) * | 2005-12-08 | 2008-09-17 | Abbott Laboratories | 9-membered heterobicyclic compounds as inhibitors of protein kinases |
| GB0525164D0 (en) | 2005-12-09 | 2006-01-18 | Xention Discovery Ltd | Compounds |
| TW201307354A (zh) * | 2005-12-29 | 2013-02-16 | Abbott Lab | 蛋白質激酶抑制劑 |
| AU2007215161A1 (en) * | 2006-02-14 | 2007-08-23 | Vertex Pharmaceuticals Incorporated | Pyrrolo(3,2-C) pyridines useful as inhibitors of protein kinases |
| US7932390B2 (en) * | 2006-06-29 | 2011-04-26 | Hoffman-La Roche Inc. | Substituted thieno[3,2-C]pyridine carboxylic acid derivatives |
| US7994321B2 (en) * | 2006-08-08 | 2011-08-09 | Hoffmann-La Roche Inc. | Substituted thieno[3,2-C]pyridine-7-carboxylic acid derivatives |
| WO2008018881A1 (en) * | 2006-08-10 | 2008-02-14 | Osi Pharmaceuticals, Inc. | 6,6-bicyclic ring substituted sulfur containing heterobicyclic protein kinase inhibitors |
| MX2010001636A (es) * | 2007-08-14 | 2010-03-15 | Hoffmann La Roche | Derivados de pirazolo[3,4-d]-pirimidina como agentes antiproliferativos. |
| AR070317A1 (es) * | 2008-02-06 | 2010-03-31 | Osi Pharm Inc | Furo (3,2-c) piridina y tieno (3,2-c) piridinas |
| CA2723358A1 (en) * | 2008-05-05 | 2009-11-12 | Allison B. Reiss | Method for improving cardiovascular risk profile of cox inhibitors |
| ES2524966T3 (es) * | 2008-12-05 | 2014-12-16 | Abbvie Bahamas Ltd. | Derivados de tieno[3,2-c]piridina como inhibidores de quinasas para uso en el tratamiento del cáncer |
| CN102574843B (zh) * | 2009-10-22 | 2015-06-17 | 法博太科制药有限公司 | 抗纤维化剂的稠环类似物 |
| WO2011156473A1 (en) * | 2010-06-09 | 2011-12-15 | Abbott Laboratories | Crystalline forms of kinase inhibitors |
| TWI492949B (zh) * | 2010-06-09 | 2015-07-21 | Abbvie Bahamas Ltd | 結晶型激酶抑制劑 |
| TWI482770B (zh) * | 2010-06-09 | 2015-05-01 | Abbvie Bahamas Ltd | 結晶型激酶抑制劑 |
| MX2012014487A (es) | 2010-07-02 | 2013-02-21 | Alcon Res Ltd | Compuestos para el tratamiento de transtornos y enfermedades del segmento posterior. |
| SG189837A1 (en) * | 2010-10-08 | 2013-06-28 | Abbvie Inc | FURO[3,2-d]PYRIMIDINE COMPOUNDS |
| US8436179B2 (en) | 2011-07-20 | 2013-05-07 | Abbvie Inc. | Kinase inhibitor with improved solubility profile |
| CN103396414B (zh) * | 2013-07-16 | 2015-06-03 | 浙江医药高等专科学校 | 咪唑取代的噻唑并环己烷类化合物、及其抗肿瘤用途 |
| CN104945411B (zh) * | 2014-03-27 | 2018-07-31 | 南京勇山生物科技有限公司 | 噻吩并[3,2-c]吡啶类化合物、其制备方法及应用 |
| WO2015157360A1 (en) | 2014-04-08 | 2015-10-15 | Abbvie Inc. | Processes to make protein kinase inhibitors |
| WO2016047678A1 (ja) * | 2014-09-25 | 2016-03-31 | 武田薬品工業株式会社 | 複素環化合物 |
| MX2019009235A (es) | 2017-02-03 | 2019-12-11 | Certa Therapeutics Pty Ltd | Compuestos antifibroticos. |
| JP2023549540A (ja) | 2020-11-18 | 2023-11-27 | デシフェラ・ファーマシューティカルズ，エルエルシー | Ｇｃｎ２およびｐｅｒｋキナーゼ阻害剤およびその使用方法 |
Citations (2)
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| WO2000039108A1 (en) * | 1998-12-23 | 2000-07-06 | Du Pont Pharmaceuticals Company | Thrombin or factor xa inhibitors |
| WO2001019828A2 (en) * | 1999-09-17 | 2001-03-22 | Basf Aktiengesellschaft | Kinase inhibitors as therapeutic agents |
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| EP1025102B1 (en) * | 1997-10-20 | 2004-05-19 | F. Hoffmann-La Roche Ag | Bicyclic kinase inhibitors |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| KR100774855B1 (ko) * | 2000-04-27 | 2007-11-08 | 아스텔라스세이야쿠 가부시키가이샤 | 축합 헤테로아릴 유도체 |
| EP1373240B1 (en) * | 2001-03-14 | 2005-06-15 | Eli Lilly And Company | Retinoid x receptor modulators |
| JP2005508904A (ja) * | 2001-09-11 | 2005-04-07 | スミスクライン ビーチャム コーポレーション | 血管新生阻害剤としてのフロ−及びチエノピリミジン誘導体 |
| JP2006528685A (ja) * | 2003-05-06 | 2006-12-21 | スミスクライン ビーチャム コーポレーション | 新規化合物 |
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2009
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000039108A1 (en) * | 1998-12-23 | 2000-07-06 | Du Pont Pharmaceuticals Company | Thrombin or factor xa inhibitors |
| WO2001019828A2 (en) * | 1999-09-17 | 2001-03-22 | Basf Aktiengesellschaft | Kinase inhibitors as therapeutic agents |
Also Published As
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| DE602004018780D1 (de) | 2009-02-12 |
| CN103087078A (zh) | 2013-05-08 |
| CA2532982C (en) | 2013-11-26 |
| AU2004259765A1 (en) | 2005-02-03 |
| ATE419253T1 (de) | 2009-01-15 |
| AU2009251083A1 (en) | 2010-01-21 |
| KR101120936B1 (ko) | 2012-03-29 |
| PL1648905T3 (pl) | 2009-07-31 |
| JP2006528646A (ja) | 2006-12-21 |
| IL173348A (en) | 2015-11-30 |
| WO2005010009A1 (en) | 2005-02-03 |
| KR20060056344A (ko) | 2006-05-24 |
| PT1648905E (pt) | 2009-04-08 |
| CA2532982A1 (en) | 2005-02-03 |
| US20050026944A1 (en) | 2005-02-03 |
| CY1111599T1 (el) | 2015-10-07 |
| JP4707192B2 (ja) | 2011-06-22 |
| BRPI0412894A (pt) | 2006-10-03 |
| EP1648905A1 (en) | 2006-04-26 |
| NZ544712A (en) | 2009-09-25 |
| AU2009251083B2 (en) | 2012-02-16 |
| EP1648905B1 (en) | 2008-12-31 |
| DK1648905T3 (da) | 2009-03-30 |
| IL173348A0 (en) | 2006-06-11 |
| ES2319302T3 (es) | 2009-05-06 |
| KR20110123797A (ko) | 2011-11-15 |
| MXPA06000919A (es) | 2006-05-04 |
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