CN104603124B - 用作布鲁顿酪氨酸激酶(btk)抑制剂的杂芳族化合物 - Google Patents
用作布鲁顿酪氨酸激酶(btk)抑制剂的杂芳族化合物 Download PDFInfo
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- CN104603124B CN104603124B CN201380041869.4A CN201380041869A CN104603124B CN 104603124 B CN104603124 B CN 104603124B CN 201380041869 A CN201380041869 A CN 201380041869A CN 104603124 B CN104603124 B CN 104603124B
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- 0 CC(C1)CC1(CC1)CC*1C(C#CC)=O Chemical compound CC(C1)CC1(CC1)CC*1C(C#CC)=O 0.000 description 19
- KPLWTAHOBWGMQQ-GQCTYLIASA-N CC(C)C(CCC1)CN1C(/C=C/CN(C1)CC1O)=O Chemical compound CC(C)C(CCC1)CN1C(/C=C/CN(C1)CC1O)=O KPLWTAHOBWGMQQ-GQCTYLIASA-N 0.000 description 1
- JJLAQLQGXMEKKL-FNORWQNLSA-N CC(C)C(CCC1)CN1C(/C=C/CN(CC1)CCC1S(C)(=O)=O)=O Chemical compound CC(C)C(CCC1)CN1C(/C=C/CN(CC1)CCC1S(C)(=O)=O)=O JJLAQLQGXMEKKL-FNORWQNLSA-N 0.000 description 1
- LJPFMLOMMFDNRN-UHFFFAOYSA-N CC(C)c1cc(NS(c2ccc(C)cc2)(=O)=O)ccc1 Chemical compound CC(C)c1cc(NS(c2ccc(C)cc2)(=O)=O)ccc1 LJPFMLOMMFDNRN-UHFFFAOYSA-N 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N CN(C)C(C=C)=O Chemical compound CN(C)C(C=C)=O YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Cc1ccccc1 Chemical compound Cc1ccccc1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- ORNRPEJYZFFIGQ-UHFFFAOYSA-N NC(c1c(N)[n](C2CCNCC2)nc1-c(cc1)ccc1O)=O Chemical compound NC(c1c(N)[n](C2CCNCC2)nc1-c(cc1)ccc1O)=O ORNRPEJYZFFIGQ-UHFFFAOYSA-N 0.000 description 1
- LQFDQJDIWFMWHN-OWOJBTEDSA-N OC(/C=C/CN1CCOCC1)=O Chemical compound OC(/C=C/CN1CCOCC1)=O LQFDQJDIWFMWHN-OWOJBTEDSA-N 0.000 description 1
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D417/08—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Transplantation (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Otolaryngology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261681684P | 2012-08-10 | 2012-08-10 | |
| US61/681,684 | 2012-08-10 | ||
| PCT/US2013/054096 WO2014025976A1 (en) | 2012-08-10 | 2013-08-08 | Heteroaromatic compounds as bruton's tyrosine kinase (btk) inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104603124A CN104603124A (zh) | 2015-05-06 |
| CN104603124B true CN104603124B (zh) | 2018-04-17 |
Family
ID=49029216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380041869.4A Expired - Fee Related CN104603124B (zh) | 2012-08-10 | 2013-08-08 | 用作布鲁顿酪氨酸激酶(btk)抑制剂的杂芳族化合物 |
Country Status (24)
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20140045813A1 (en) | 2012-08-10 | 2014-02-13 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as btk inhibitors |
| WO2014068527A1 (en) * | 2012-11-02 | 2014-05-08 | Pfizer Inc. | Bruton's tyrosine kinase inhibitors |
| CN103848810A (zh) * | 2012-11-30 | 2014-06-11 | 北京赛林泰医药技术有限公司 | 鲁顿酪氨酸激酶抑制剂 |
| EP2970163B1 (en) * | 2013-03-14 | 2018-02-28 | Boehringer Ingelheim International GmbH | 5-thiazolecarboxamide dervatives and their use as btk inhibitors |
| EP2970300B1 (en) | 2013-03-15 | 2018-05-16 | Boehringer Ingelheim International GmbH | Heteroaromatic compounds as btk inhibitors |
| KR102311329B1 (ko) * | 2013-03-15 | 2021-10-14 | 얀센 파마슈티카 엔.브이. | 약제를 제조하기 위한 방법 및 중간체 |
| WO2015048662A2 (en) * | 2013-09-30 | 2015-04-02 | X-Rx Discovery, Inc. | Substituted nicotinimide inhibitors of btk and their preparation and use in the treatment of cancer, inflammation and autoimmune disease |
| US9512084B2 (en) | 2013-11-29 | 2016-12-06 | Novartis Ag | Amino pyrimidine derivatives |
| EP3099674B1 (en) * | 2014-01-29 | 2018-10-24 | Boehringer Ingelheim International Gmbh | Pyrazole compounds as btk inhibitors |
| WO2015185998A2 (en) * | 2014-04-11 | 2015-12-10 | Acerta Pharma B.V. | Methods of blocking the cxcr-4/sdf-1 signaling pathway with inhibitors of bone marrow x kinase |
| CN105085474B (zh) * | 2014-05-07 | 2018-05-18 | 北京赛林泰医药技术有限公司 | 鲁顿酪氨酸激酶抑制剂 |
| CN105884747B (zh) * | 2014-08-28 | 2021-01-05 | 首药控股(北京)有限公司 | 一种制备布鲁顿酪氨酸激酶(btk)激酶抑制剂的制备方法 |
| GB201519352D0 (en) | 2015-11-02 | 2015-12-16 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| CA3005268C (en) | 2015-12-16 | 2024-04-30 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as btk inhibitors |
| CN114605327B (zh) | 2015-12-16 | 2025-03-11 | 洛克索肿瘤学股份有限公司 | 可用作激酶抑制剂的化合物 |
| CN105646318A (zh) * | 2015-12-30 | 2016-06-08 | 武汉药明康德新药开发有限公司 | 一种2-叔丁氧羰基-5-氮杂螺环[3.3]庚烷-6-羧酸的合成方法 |
| JP6916185B2 (ja) | 2016-01-13 | 2021-08-11 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Btk阻害剤としてのイソキノロン類 |
| CN107226805A (zh) * | 2016-03-24 | 2017-10-03 | 北京天诚医药科技有限公司 | 芳香族酰胺类衍生物、其制备方法及其在医药上的应用 |
| JP6851391B2 (ja) * | 2016-08-15 | 2021-03-31 | ノバルティス アーゲー | オファツムマブを用いた多発性硬化症の治療レジメンおよび治療方法 |
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