CN101460466B - 适用作蛋白激酶抑制剂的噻唑类、咪唑类和吡唑类 - Google Patents
适用作蛋白激酶抑制剂的噻唑类、咪唑类和吡唑类 Download PDFInfo
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- CN101460466B CN101460466B CN2007800208154A CN200780020815A CN101460466B CN 101460466 B CN101460466 B CN 101460466B CN 2007800208154 A CN2007800208154 A CN 2007800208154A CN 200780020815 A CN200780020815 A CN 200780020815A CN 101460466 B CN101460466 B CN 101460466B
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- 0 *OC(C(C=C(C1)I)=C1C(CC1)=CC=C1[Tl]*)N Chemical compound *OC(C(C=C(C1)I)=C1C(CC1)=CC=C1[Tl]*)N 0.000 description 6
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/587—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with aliphatic hydrocarbon radicals substituted by 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 ring carbon atoms, said aliphatic radicals being substituted in the alpha-position to the ring by a hetero atom, e.g. with m >= 0, Z being a singly or a doubly bound hetero atom
- C07D277/593—Z being doubly bound oxygen or doubly bound nitrogen, which nitrogen is part of a possibly substituted oximino radical
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Endocrinology (AREA)
- Communicable Diseases (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Obesity (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79108306P | 2006-04-11 | 2006-04-11 | |
| US60/791,083 | 2006-04-11 | ||
| PCT/US2007/008819 WO2007117692A2 (en) | 2006-04-11 | 2007-04-11 | Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101460466A CN101460466A (zh) | 2009-06-17 |
| CN101460466B true CN101460466B (zh) | 2012-06-13 |
Family
ID=38508761
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2007800208154A Expired - Fee Related CN101460466B (zh) | 2006-04-11 | 2007-04-11 | 适用作蛋白激酶抑制剂的噻唑类、咪唑类和吡唑类 |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US7589214B2 (https=) |
| EP (1) | EP2007732B1 (https=) |
| JP (1) | JP2009536617A (https=) |
| CN (1) | CN101460466B (https=) |
| AT (1) | ATE534632T1 (https=) |
| AU (1) | AU2007235237B2 (https=) |
| CA (1) | CA2648923A1 (https=) |
| ES (1) | ES2376765T3 (https=) |
| WO (1) | WO2007117692A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10301297B2 (en) | 2013-09-30 | 2019-05-28 | Guangzhou Innocare Pharma Tech Co., Ltd. | Substituted nicotinimide inhibitors of BTK and their preparation and use in the treatment of cancer, inflammation and autoimmune disease |
| RU2810260C2 (ru) * | 2019-02-25 | 2023-12-25 | Бэйцзин Иннокэа Фарма Тек Ко., Лтд. | Способ получения 6-(1-акрилоилпиперидин-4-ил)-2-(4-феноксифенил)никотинамида |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2648923A1 (en) * | 2006-04-11 | 2007-10-18 | Vertex Pharmaceuticals Incorporated | Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases |
| MX2011011136A (es) * | 2009-04-24 | 2011-11-18 | Tibotec Pharm Ltd | Eteres diarilicos. |
| EP2512246B1 (en) | 2009-12-17 | 2015-09-30 | Merck Sharp & Dohme Corp. | Aminopyrimidines as syk inhibitors |
| KR101445012B1 (ko) | 2009-12-17 | 2014-09-26 | 머크 샤프 앤드 돔 코포레이션 | Syk 억제제로서의 아미노피리미딘 |
| US9145391B2 (en) | 2011-05-10 | 2015-09-29 | Merck Sharp & Dohme Corp. | Bipyridylaminopyridines as Syk inhibitors |
| EP2706853B1 (en) | 2011-05-10 | 2017-06-14 | Merck Sharp & Dohme Corp. | Aminopyrimidines as syk inhibitors |
| CA2834062A1 (en) | 2011-05-10 | 2012-11-15 | Merck Sharp & Dohme Corp. | Pyridyl aminopyridines as syk inhibitors |
| MX340033B (es) | 2011-12-28 | 2016-06-21 | Janssen Sciences Ireland Uc | Derivados heterobiciclicos como inhibidores del virus de la hepatitis c. |
| SG11201500499TA (en) | 2012-08-10 | 2015-03-30 | Boehringer Ingelheim Int | Heteroaromatic compounds as bruton's tyrosine kinase (btk) inhibitors |
| KR101668574B1 (ko) | 2012-11-02 | 2016-10-24 | 화이자 인코포레이티드 | 브루톤 티로신 키나제 억제제 |
| 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 |
| JP6403751B2 (ja) | 2013-03-14 | 2018-10-10 | 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 | 5−チアゾールカルボキサミン誘導体及びbtk阻害剤としてのその使用 |
| JP6495886B2 (ja) | 2013-03-15 | 2019-04-03 | 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阻害剤としての複素環式芳香族化合物 |
| RU2653504C2 (ru) | 2013-12-13 | 2018-05-10 | Ф. Хоффманн-Ля Рош Аг | Ингибиторы тирозинкиназы брутона |
| JP6486954B2 (ja) * | 2014-01-29 | 2019-03-20 | 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阻害剤としてのピラゾール化合物 |
| 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 |
| CN106687446B (zh) * | 2014-07-18 | 2020-04-28 | 百济神州(北京)生物科技有限公司 | 作为t790m/wt-egfr的选择性和不可逆的激酶抑制剂的5-氨基-4-氨甲酰基-吡唑化合物及其用途 |
| LT3390390T (lt) | 2015-12-16 | 2021-11-25 | Boehringer Ingelheim International Gmbh | Bipirazolilo dariniai, tinkami naudoti autoimuninių ligų gydymui |
| US10570118B2 (en) | 2016-01-13 | 2020-02-25 | Boehringer Ingelheim International Gmbh | Isoquinolones as BTK inhibitors |
| AU2020229919B2 (en) | 2019-02-25 | 2025-06-05 | Beijing Innocare Pharma Tech Co., Ltd. | Process for preparing 6- (1-Acryloylpiperidin-4-yl) -2- (4-phenoxyphenyl) nicotinamide |
| CN116018138B (zh) * | 2020-07-13 | 2025-08-15 | 河南知微生物医药有限公司 | 作为布鲁诺酪氨酸激酶抑制剂的取代的1H-咪唑并[1,2-b]吡唑-3-甲酰胺 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1473161A (zh) * | 2000-09-15 | 2004-02-04 | ��̩��˹ҩ��ɷ�����˾ | 可用作蛋白激酶抑制剂的吡唑化合物 |
| WO2005012256A1 (en) * | 2003-07-22 | 2005-02-10 | Astex Therapeutics Limited | 3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9608435D0 (en) * | 1996-04-24 | 1996-06-26 | Celltech Therapeutics Ltd | Chemical compounds |
| US6288061B1 (en) * | 1997-12-26 | 2001-09-11 | Welfide Corporation | Imidazole derivatives |
| ES2274005T3 (es) * | 2001-01-26 | 2007-05-16 | Chugai Seiyaku Kabushiki Kaisha | Inhibidores de malonyl-coa decarboxilasa usados como moduladores metabolicos. |
| WO2005123671A1 (ja) * | 2004-06-22 | 2005-12-29 | Taisho Pharmaceutical Co., Ltd. | ピロール誘導体 |
| FR2881426B1 (fr) | 2005-02-03 | 2007-03-30 | Aventis Pharma Sa | Pyrolles et imidazoles substitues, compositions les contenant, procede de frabrication et utilisation |
| CA2648923A1 (en) * | 2006-04-11 | 2007-10-18 | Vertex Pharmaceuticals Incorporated | Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases |
-
2007
- 2007-04-11 CA CA002648923A patent/CA2648923A1/en not_active Abandoned
- 2007-04-11 WO PCT/US2007/008819 patent/WO2007117692A2/en not_active Ceased
- 2007-04-11 JP JP2009505430A patent/JP2009536617A/ja active Pending
- 2007-04-11 CN CN2007800208154A patent/CN101460466B/zh not_active Expired - Fee Related
- 2007-04-11 ES ES07755181T patent/ES2376765T3/es active Active
- 2007-04-11 AT AT07755181T patent/ATE534632T1/de active
- 2007-04-11 EP EP07755181A patent/EP2007732B1/en not_active Not-in-force
- 2007-04-11 AU AU2007235237A patent/AU2007235237B2/en not_active Ceased
- 2007-04-11 US US11/786,464 patent/US7589214B2/en not_active Expired - Fee Related
-
2009
- 2009-08-10 US US12/538,396 patent/US8236832B2/en not_active Expired - Fee Related
-
2012
- 2012-07-03 US US13/540,651 patent/US8865751B2/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1473161A (zh) * | 2000-09-15 | 2004-02-04 | ��̩��˹ҩ��ɷ�����˾ | 可用作蛋白激酶抑制剂的吡唑化合物 |
| WO2005012256A1 (en) * | 2003-07-22 | 2005-02-10 | Astex Therapeutics Limited | 3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10301297B2 (en) | 2013-09-30 | 2019-05-28 | Guangzhou Innocare Pharma Tech Co., Ltd. | Substituted nicotinimide inhibitors of BTK and their preparation and use in the treatment of cancer, inflammation and autoimmune disease |
| US11345695B2 (en) | 2013-09-30 | 2022-05-31 | Guangzhou Innocare Pharma Tech Co., Ltd. | Substituted nicotinimide inhibitors of BTK and their preparation and use in the treatment of cancer, inflammation and autoimmune disease |
| US11840513B2 (en) | 2013-09-30 | 2023-12-12 | Guangzhou Innocare Pharma Tech Co., Ltd | Substituted nicotinimide inhibitors of BTK for treating cancer |
| RU2810260C2 (ru) * | 2019-02-25 | 2023-12-25 | Бэйцзин Иннокэа Фарма Тек Ко., Лтд. | Способ получения 6-(1-акрилоилпиперидин-4-ил)-2-(4-феноксифенил)никотинамида |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2007235237A1 (en) | 2007-10-18 |
| ATE534632T1 (de) | 2011-12-15 |
| US20130090479A1 (en) | 2013-04-11 |
| CA2648923A1 (en) | 2007-10-18 |
| EP2007732A2 (en) | 2008-12-31 |
| US20090306155A1 (en) | 2009-12-10 |
| US8865751B2 (en) | 2014-10-21 |
| EP2007732B1 (en) | 2011-11-23 |
| ES2376765T3 (es) | 2012-03-16 |
| US8236832B2 (en) | 2012-08-07 |
| JP2009536617A (ja) | 2009-10-15 |
| AU2007235237B2 (en) | 2011-08-18 |
| WO2007117692A2 (en) | 2007-10-18 |
| CN101460466A (zh) | 2009-06-17 |
| US7589214B2 (en) | 2009-09-15 |
| US20070298065A1 (en) | 2007-12-27 |
| WO2007117692A3 (en) | 2008-01-10 |
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