CN102361859A - 用作Raf激酶抑制剂的杂芳基化合物 - Google Patents
用作Raf激酶抑制剂的杂芳基化合物 Download PDFInfo
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- CN102361859A CN102361859A CN2009801577085A CN200980157708A CN102361859A CN 102361859 A CN102361859 A CN 102361859A CN 2009801577085 A CN2009801577085 A CN 2009801577085A CN 200980157708 A CN200980157708 A CN 200980157708A CN 102361859 A CN102361859 A CN 102361859A
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- Prior art keywords
- ring
- compound
- nitrogen
- optionally substituted
- sulfur
- Prior art date
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- 0 *C1(CC1)N(*)C1(/C2=C\C=C\C=C\C=C2)OC1 Chemical compound *C1(CC1)N(*)C1(/C2=C\C=C\C=C\C=C2)OC1 0.000 description 8
- WJIRZSFTHVYWQK-UHFFFAOYSA-N CC(C)(C)OC(NC(C)(C)c1n[o]c(C(OC)=O)c1)=O Chemical compound CC(C)(C)OC(NC(C)(C)c1n[o]c(C(OC)=O)c1)=O WJIRZSFTHVYWQK-UHFFFAOYSA-N 0.000 description 1
- IUJLFXOATISXLC-UHFFFAOYSA-N CC(C)Oc1cc(C(F)(F)F)ccc1Nc1ncc(C(C)NC(c2ncc3nc[n](C)c3c2)=O)[s]1 Chemical compound CC(C)Oc1cc(C(F)(F)F)ccc1Nc1ncc(C(C)NC(c2ncc3nc[n](C)c3c2)=O)[s]1 IUJLFXOATISXLC-UHFFFAOYSA-N 0.000 description 1
- JSVBMXCFOYVJKZ-UHFFFAOYSA-N CC(c1cc(C(Nc2cc(C(F)(F)F)ccc2)=O)n[o]1)NC(OC(C)(C)C)=O Chemical compound CC(c1cc(C(Nc2cc(C(F)(F)F)ccc2)=O)n[o]1)NC(OC(C)(C)C)=O JSVBMXCFOYVJKZ-UHFFFAOYSA-N 0.000 description 1
- HVFZBLQOBVBPKT-UHFFFAOYSA-N CC(c1cnc(Nc2ccc(C(F)(F)F)cc2)[s]1)NCc(nc1)c[n]2c1ncc2Br Chemical compound CC(c1cnc(Nc2ccc(C(F)(F)F)cc2)[s]1)NCc(nc1)c[n]2c1ncc2Br HVFZBLQOBVBPKT-UHFFFAOYSA-N 0.000 description 1
- QJQVAGHLAJHHSM-UHFFFAOYSA-N CC(c1n[o]c(C(OC)=O)c1)NC(c1c(cccc2)[n]2nc1)=O Chemical compound CC(c1n[o]c(C(OC)=O)c1)NC(c1c(cccc2)[n]2nc1)=O QJQVAGHLAJHHSM-UHFFFAOYSA-N 0.000 description 1
- RQWBBKJCUKJZFC-FXADVQPWSA-N C[C@H](C(C1)=NOC1(C)C(Nc(cc1C(F)(F)F)ccc1Br)=O)NC(c1c(cccc2)[n]2nc1)=O Chemical compound C[C@H](C(C1)=NOC1(C)C(Nc(cc1C(F)(F)F)ccc1Br)=O)NC(c1c(cccc2)[n]2nc1)=O RQWBBKJCUKJZFC-FXADVQPWSA-N 0.000 description 1
- GEBGQCAIKGCPSX-SSDOTTSWSA-N C[C@H](c1cc(C(Nc2cccc(C(F)(F)F)c2)=O)n[o]1)N Chemical compound C[C@H](c1cc(C(Nc2cccc(C(F)(F)F)c2)=O)n[o]1)N GEBGQCAIKGCPSX-SSDOTTSWSA-N 0.000 description 1
- QHPHGGWCQRZOIQ-ZCFIWIBFSA-N C[C@H](c1cc(C(O)=O)n[o]1)NC(OC(C)(C)C)=O Chemical compound C[C@H](c1cc(C(O)=O)n[o]1)NC(OC(C)(C)C)=O QHPHGGWCQRZOIQ-ZCFIWIBFSA-N 0.000 description 1
- YRTICVAGGMGXEM-MRVPVSSYSA-N C[C@H](c1n[o]c(C(O)=O)c1)NC(c1c(cccc2)[n]2nc1)=O Chemical compound C[C@H](c1n[o]c(C(O)=O)c1)NC(c1c(cccc2)[n]2nc1)=O YRTICVAGGMGXEM-MRVPVSSYSA-N 0.000 description 1
- YCWXBAPXLSOKGP-SNVBAGLBSA-N C[C@H](c1ncc(C(Nc(cc2C(F)(F)F)ncc2Cl)=O)[s]1)NC(c1cnc(C2)[n]1CCN2C(C)=N)=O Chemical compound C[C@H](c1ncc(C(Nc(cc2C(F)(F)F)ncc2Cl)=O)[s]1)NC(c1cnc(C2)[n]1CCN2C(C)=N)=O YCWXBAPXLSOKGP-SNVBAGLBSA-N 0.000 description 1
- MOOKIBJOWMZDEK-UHFFFAOYSA-N OC(c(nc1)c[n]2c1ncc2Br)=O Chemical compound OC(c(nc1)c[n]2c1ncc2Br)=O MOOKIBJOWMZDEK-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D471/00—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
- 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
- C07D471/04—Ortho-condensed systems
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Pulmonology (AREA)
- Transplantation (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Reproductive Health (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Virology (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14156108P | 2008-12-30 | 2008-12-30 | |
| US61/141,561 | 2008-12-30 | ||
| PCT/US2009/069795 WO2010078408A1 (en) | 2008-12-30 | 2009-12-30 | Heteroaryl compounds useful as raf kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102361859A true CN102361859A (zh) | 2012-02-22 |
Family
ID=41719139
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801577085A Pending CN102361859A (zh) | 2008-12-30 | 2009-12-30 | 用作Raf激酶抑制剂的杂芳基化合物 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20120040951A1 (https=) |
| EP (1) | EP2379513A1 (https=) |
| JP (1) | JP2012514044A (https=) |
| CN (1) | CN102361859A (https=) |
| AU (1) | AU2009334997A1 (https=) |
| CA (1) | CA2748274A1 (https=) |
| IL (1) | IL213601A0 (https=) |
| MX (1) | MX2011006997A (https=) |
| WO (1) | WO2010078408A1 (https=) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102924446A (zh) * | 2011-08-11 | 2013-02-13 | 上海吉铠医药科技有限公司 | Pim激酶抑制剂及其制备方法与在制药中的应用 |
| CN105384738A (zh) * | 2014-08-21 | 2016-03-09 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
| CN106029072A (zh) * | 2013-08-28 | 2016-10-12 | 麦迪韦逊技术股份有限公司 | 杂环化合物和使用方法 |
| CN117143095A (zh) * | 2023-08-03 | 2023-12-01 | 苏州汉德创宏生化科技有限公司 | 一种6-溴吡唑并[1,5-a]吡啶-3-羧酸及其制备方法 |
| CN117567388A (zh) * | 2023-11-14 | 2024-02-20 | 济南悟通生物科技有限公司 | 一种2-乙酰基-5-噻唑甲酸的合成方法 |
| CN119241529A (zh) * | 2024-09-20 | 2025-01-03 | 武汉九州钰民医药科技有限公司 | 一种Tovorafenib的制备方法 |
| CN119241530A (zh) * | 2024-09-20 | 2025-01-03 | 武汉九州钰民医药科技有限公司 | 一种Tovorafenib的药物合成工艺 |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR067354A1 (es) | 2007-06-29 | 2009-10-07 | Sunesis Pharmaceuticals Inc | Compuestos utiles como inhibidores de la raf quinasa |
| EP2167497A2 (en) | 2007-06-29 | 2010-03-31 | Sunesis Pharmaceuticals, Inc. | Heterocyclic compounds useful as raf kinase inhibitors |
| JP2011057661A (ja) * | 2009-08-14 | 2011-03-24 | Bayer Cropscience Ag | 殺虫性カルボキサミド類 |
| CN102574833B (zh) * | 2009-10-12 | 2014-08-20 | 拜尔农作物科学股份公司 | 用作杀虫剂的酰胺和硫代酰胺 |
| US9290485B2 (en) | 2010-08-04 | 2016-03-22 | Novartis Ag | N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides |
| EP2627324A4 (en) * | 2010-10-11 | 2014-05-07 | Univ Leland Stanford Junior | SUBSTITUTED BENZAMIDES AND USES THEREOF |
| CN102250065B (zh) * | 2011-05-20 | 2015-05-13 | 浙江海正药业股份有限公司 | 取代的三嗪苯脲衍生物及其用途 |
| WO2012166463A2 (en) * | 2011-05-27 | 2012-12-06 | Neosome Life Sciences, LLC | Aminooxazole inhibitors of cyclin dependent kinases |
| US9452995B2 (en) | 2011-08-11 | 2016-09-27 | Jikai Biosciences, Inc. | Pyridine derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof |
| US9453003B2 (en) | 2011-08-11 | 2016-09-27 | Jikai Biosciences, Inc. | Pyrimidine derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof |
| US9458151B2 (en) | 2011-08-11 | 2016-10-04 | Jikai Biosciences, Inc. | Isothiazole derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| US9296732B2 (en) | 2012-04-12 | 2016-03-29 | The Board Of Trustees Of The Leland Stanford Junior University | Substituted benzamides and their uses |
| IN2015DN00659A (https=) * | 2012-08-07 | 2015-06-26 | Janssen Pharmaceutica Nv | |
| GB201401886D0 (en) | 2014-02-04 | 2014-03-19 | Lytix Biopharma As | Neurodegenerative therapies |
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| EA039916B1 (ru) * | 2015-10-23 | 2022-03-28 | Вифор (Интернациональ) Аг | Новые ингибиторы ферропортина |
| JP2019518046A (ja) | 2016-06-16 | 2019-06-27 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | 抗菌薬としての複素環式化合物 |
| JP7341060B2 (ja) | 2017-02-10 | 2023-09-08 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | Mapk経路の活性化に関連付けられる癌の処置のための方法及び医薬組成物 |
| KR20190121315A (ko) | 2017-03-01 | 2019-10-25 | 얀센 사이언시즈 아일랜드 언리미티드 컴퍼니 | 병용 요법 |
| US11124509B2 (en) | 2017-03-23 | 2021-09-21 | Clavius Pharmaceuticals, LLC. | Tri-substituted imidazoles for the inhibition of TGF beta and methods of treatment |
| JOP20180036A1 (ar) | 2017-04-18 | 2019-01-30 | Vifor Int Ag | أملاح لمثبطات فروبورتين جديدة |
| EP3732285A1 (en) | 2017-12-28 | 2020-11-04 | Tract Pharmaceuticals, Inc. | Stem cell culture systems for columnar epithelial stem cells, and uses related thereto |
| US12077548B2 (en) | 2018-08-22 | 2024-09-03 | Clavius Pharmaceuticals, LLC. | Substituted imidazoles for the inhibition of TGF-β and methods of treatment |
| US10927111B2 (en) | 2019-05-03 | 2021-02-23 | Kinnate Biopharma Inc. | Inhibitors of RAF kinases |
| BR112022007612A2 (pt) | 2019-10-24 | 2022-09-20 | Kinnate Biopharma Inc | Inibidores de raf quinases |
| US11407737B2 (en) | 2020-09-18 | 2022-08-09 | Kinnate Biopharma Inc. | Inhibitors of RAF kinases |
| WO2022081469A1 (en) | 2020-10-12 | 2022-04-21 | Kinnate Biopharma Inc. | Inhibitors of raf kinases |
| CN112535793B (zh) * | 2020-11-19 | 2021-10-08 | 融冲(深圳)生物医疗科技有限责任公司 | 药物涂层球囊导管的制备方法与应用 |
| CN117561057A (zh) | 2021-04-23 | 2024-02-13 | 金耐特生物制药公司 | 用raf抑制剂治疗癌症 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0847992A1 (en) * | 1996-09-30 | 1998-06-17 | Mitsui Chemicals, Inc. | Benzamide derivatives, useful as cell differentiation inducers |
| EP1547585A1 (en) * | 2002-09-25 | 2005-06-29 | Santen Pharmaceutical Co., Ltd. | Therapeutic agent for rheumatism containing benzamide derivative as active ingredient |
| WO2006065703A1 (en) * | 2004-12-13 | 2006-06-22 | Sunesis Pharmaceuticals, Inc. | Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors |
| US20090005359A1 (en) * | 2007-06-29 | 2009-01-01 | Sunesis Pharmaceuticals, Inc | Heterocyclic Compounds Useful as RAF Kinase Inhibitors |
| WO2009006389A2 (en) * | 2007-06-29 | 2009-01-08 | Sunesis Pharmaceuticals, Inc. | Pyrimidine derivatives useful as raf kinase inhibitors |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5304121A (en) | 1990-12-28 | 1994-04-19 | Boston Scientific Corporation | Drug delivery system making use of a hydrogel polymer coating |
| US5886026A (en) | 1993-07-19 | 1999-03-23 | Angiotech Pharmaceuticals Inc. | Anti-angiogenic compositions and methods of use |
| US6099562A (en) | 1996-06-13 | 2000-08-08 | Schneider (Usa) Inc. | Drug coating with topcoat |
| JP2003073357A (ja) | 2001-09-03 | 2003-03-12 | Mitsubishi Pharma Corp | アミド化合物を含有するRhoキナーゼ阻害剤 |
-
2009
- 2009-12-30 WO PCT/US2009/069795 patent/WO2010078408A1/en not_active Ceased
- 2009-12-30 JP JP2011544601A patent/JP2012514044A/ja not_active Withdrawn
- 2009-12-30 MX MX2011006997A patent/MX2011006997A/es not_active Application Discontinuation
- 2009-12-30 AU AU2009334997A patent/AU2009334997A1/en not_active Abandoned
- 2009-12-30 CN CN2009801577085A patent/CN102361859A/zh active Pending
- 2009-12-30 US US13/142,603 patent/US20120040951A1/en not_active Abandoned
- 2009-12-30 EP EP09795675A patent/EP2379513A1/en not_active Withdrawn
- 2009-12-30 CA CA2748274A patent/CA2748274A1/en not_active Abandoned
-
2011
- 2011-06-16 IL IL213601A patent/IL213601A0/en unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0847992A1 (en) * | 1996-09-30 | 1998-06-17 | Mitsui Chemicals, Inc. | Benzamide derivatives, useful as cell differentiation inducers |
| EP1547585A1 (en) * | 2002-09-25 | 2005-06-29 | Santen Pharmaceutical Co., Ltd. | Therapeutic agent for rheumatism containing benzamide derivative as active ingredient |
| WO2006065703A1 (en) * | 2004-12-13 | 2006-06-22 | Sunesis Pharmaceuticals, Inc. | Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors |
| US20090005359A1 (en) * | 2007-06-29 | 2009-01-01 | Sunesis Pharmaceuticals, Inc | Heterocyclic Compounds Useful as RAF Kinase Inhibitors |
| WO2009006389A2 (en) * | 2007-06-29 | 2009-01-08 | Sunesis Pharmaceuticals, Inc. | Pyrimidine derivatives useful as raf kinase inhibitors |
Non-Patent Citations (3)
| Title |
|---|
| EVAN T.KELLER,等: "The role of Raf kinase inhibitor protein(RKIP) in health and disease", 《BIOCHEMICAL PHARMACOLOGY》 * |
| 彭扬,等: "Raf激酶抑制剂研究进展", 《中南药学》 * |
| 焦宇,等: "抗肿瘤药物Raf激酶抑制剂的研究进展", 《海峡药学》 * |
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|---|---|---|---|---|
| CN102924446A (zh) * | 2011-08-11 | 2013-02-13 | 上海吉铠医药科技有限公司 | Pim激酶抑制剂及其制备方法与在制药中的应用 |
| CN102924446B (zh) * | 2011-08-11 | 2015-08-26 | 上海吉铠医药科技有限公司 | Pim激酶抑制剂及其制备方法与在制药中的应用 |
| CN106029072A (zh) * | 2013-08-28 | 2016-10-12 | 麦迪韦逊技术股份有限公司 | 杂环化合物和使用方法 |
| CN105384738A (zh) * | 2014-08-21 | 2016-03-09 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
| CN117143095A (zh) * | 2023-08-03 | 2023-12-01 | 苏州汉德创宏生化科技有限公司 | 一种6-溴吡唑并[1,5-a]吡啶-3-羧酸及其制备方法 |
| CN117567388A (zh) * | 2023-11-14 | 2024-02-20 | 济南悟通生物科技有限公司 | 一种2-乙酰基-5-噻唑甲酸的合成方法 |
| CN117567388B (zh) * | 2023-11-14 | 2024-04-16 | 济南悟通生物科技有限公司 | 一种2-乙酰基-5-噻唑甲酸的合成方法 |
| CN119241529A (zh) * | 2024-09-20 | 2025-01-03 | 武汉九州钰民医药科技有限公司 | 一种Tovorafenib的制备方法 |
| CN119241530A (zh) * | 2024-09-20 | 2025-01-03 | 武汉九州钰民医药科技有限公司 | 一种Tovorafenib的药物合成工艺 |
| CN119241530B (zh) * | 2024-09-20 | 2026-04-10 | 武汉九州钰民医药科技有限公司 | 一种Tovorafenib的药物合成工艺 |
| CN119241529B (zh) * | 2024-09-20 | 2026-04-10 | 武汉九州钰民医药科技有限公司 | 一种Tovorafenib的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2748274A1 (en) | 2010-07-08 |
| US20120040951A1 (en) | 2012-02-16 |
| IL213601A0 (en) | 2011-07-31 |
| AU2009334997A1 (en) | 2011-08-04 |
| WO2010078408A1 (en) | 2010-07-08 |
| EP2379513A1 (en) | 2011-10-26 |
| JP2012514044A (ja) | 2012-06-21 |
| MX2011006997A (es) | 2011-10-21 |
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