JP5620417B2 - アミノピラゾール誘導体を含む医薬 - Google Patents
アミノピラゾール誘導体を含む医薬 Download PDFInfo
- Publication number
- JP5620417B2 JP5620417B2 JP2012023811A JP2012023811A JP5620417B2 JP 5620417 B2 JP5620417 B2 JP 5620417B2 JP 2012023811 A JP2012023811 A JP 2012023811A JP 2012023811 A JP2012023811 A JP 2012023811A JP 5620417 B2 JP5620417 B2 JP 5620417B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- amino
- methyl
- benzimidazol
- pyrazol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CC1=CC=CC*1[N+]([O-])=O Chemical compound CC1=CC=CC*1[N+]([O-])=O 0.000 description 5
- UWGHIDYMZRHNDR-UHFFFAOYSA-N CC(C)(C)OC(NN(C(OC(C)(C)C)=O)c1ccc2[nH]c(C)nc2c1)=O Chemical compound CC(C)(C)OC(NN(C(OC(C)(C)C)=O)c1ccc2[nH]c(C)nc2c1)=O UWGHIDYMZRHNDR-UHFFFAOYSA-N 0.000 description 1
- ZZBPUDYQUCPNKW-UHFFFAOYSA-N CC(C)(C)[SiH+]c1ccccc1 Chemical compound CC(C)(C)[SiH+]c1ccccc1 ZZBPUDYQUCPNKW-UHFFFAOYSA-N 0.000 description 1
- RUHFAZPQHXUEGP-UHFFFAOYSA-N CC(C12)C(CO)=CC=C1C=CN2S(c1ccccc1)(=O)=O Chemical compound CC(C12)C(CO)=CC=C1C=CN2S(c1ccccc1)(=O)=O RUHFAZPQHXUEGP-UHFFFAOYSA-N 0.000 description 1
- CIMNEJMCUZLWTJ-UHFFFAOYSA-N CC1N(C)C2C=CC(NN)=CC2N1 Chemical compound CC1N(C)C2C=CC(NN)=CC2N1 CIMNEJMCUZLWTJ-UHFFFAOYSA-N 0.000 description 1
- ZIJIMNKHXDAYCB-UHFFFAOYSA-N C[Si+](C)(C)CCOC[n]1c(cc(cc2)NN)c2nc1C(F)F Chemical compound C[Si+](C)(C)CCOC[n]1c(cc(cc2)NN)c2nc1C(F)F ZIJIMNKHXDAYCB-UHFFFAOYSA-N 0.000 description 1
- DNVWMFVLIONESY-UHFFFAOYSA-N FC(c1nc(cc(cc2)Br)c2[nH]1)F Chemical compound FC(c1nc(cc(cc2)Br)c2[nH]1)F DNVWMFVLIONESY-UHFFFAOYSA-N 0.000 description 1
- HUESKYBITFJHAL-UHFFFAOYSA-N Nc(cc1)cc(OCC2CC2)c1Cl Chemical compound Nc(cc1)cc(OCC2CC2)c1Cl HUESKYBITFJHAL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Health & Medical Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012023811A JP5620417B2 (ja) | 2011-02-07 | 2012-02-07 | アミノピラゾール誘導体を含む医薬 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011024078 | 2011-02-07 | ||
| JP2011024078 | 2011-02-07 | ||
| JP2012023811A JP5620417B2 (ja) | 2011-02-07 | 2012-02-07 | アミノピラゾール誘導体を含む医薬 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012180344A JP2012180344A (ja) | 2012-09-20 |
| JP2012180344A5 JP2012180344A5 (OSRAM) | 2014-10-02 |
| JP5620417B2 true JP5620417B2 (ja) | 2014-11-05 |
Family
ID=47011846
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012023811A Expired - Fee Related JP5620417B2 (ja) | 2011-02-07 | 2012-02-07 | アミノピラゾール誘導体を含む医薬 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5620417B2 (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3015953B1 (ja) | 1998-10-06 | 2000-03-06 | 株式会社ワールド・ブリック | れんが壁 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107501413A (zh) | 2012-09-27 | 2017-12-22 | 中外制药株式会社 | Fgfr3融合基因和以其作为标靶的药物 |
| CN103224479B (zh) * | 2013-04-26 | 2014-10-15 | 温州大学 | 一种2-芳基苯并呋喃类化合物的合成方法 |
| EP2886118B1 (en) | 2013-07-31 | 2018-09-05 | Chugai Seiyaku Kabushiki Kaisha | Pharmaceutical preparation comprising aminopyrazole derivative |
| MX367723B (es) * | 2013-10-25 | 2019-09-03 | Novartis Ag | Compuestos de anillos fusionados bicíclicos derivados de piridilo como inhibidores de fgfr4. |
| US9802920B2 (en) | 2013-12-13 | 2017-10-31 | Hoffman-La Roche Inc. | Inhibitors of bruton's tyrosine kinase |
| JP6219523B2 (ja) | 2013-12-13 | 2017-10-25 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ブルトンチロシンキナーゼの阻害剤 |
| TW201609093A (zh) * | 2013-12-27 | 2016-03-16 | Chugai Pharmaceutical Co Ltd | Fgfr門控蛋白變異基因及以其爲標的之醫藥 |
| JP2017516463A (ja) * | 2014-03-31 | 2017-06-22 | デバイオファーム インターナショナル エスエイ | Fgfr融合体 |
| EP3200786B1 (en) | 2014-10-03 | 2019-08-28 | Novartis AG | Use of ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors |
| US9802917B2 (en) * | 2015-03-25 | 2017-10-31 | Novartis Ag | Particles of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide |
| WO2016204261A1 (ja) * | 2015-06-17 | 2016-12-22 | 中外製薬株式会社 | アミノピラゾール誘導体 |
| EP3339305B1 (en) * | 2015-08-20 | 2022-05-04 | Zhejiang Hisun Pharmaceutical Co., Ltd | Indole derivative, preparation method thereof, and use thereof in pharmaceutical drug |
| CN110950848B (zh) * | 2018-09-27 | 2024-03-26 | 徐诺药业 | 新型氨基吡唑类衍生物的合成与应用 |
| EP3898626A1 (en) * | 2018-12-19 | 2021-10-27 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| JP2022515197A (ja) | 2018-12-19 | 2022-02-17 | アレイ バイオファーマ インコーポレイテッド | がんを治療するためのfgfr阻害剤としての7-((3,5-ジメトキシフェニル)アミノ)キノキサリン誘導体 |
| CN112358435B (zh) * | 2019-10-12 | 2023-01-10 | 中国医学科学院医药生物技术研究所 | 取代芳并杂环类化合物、制备方法和抑制ulk1及抗肿瘤用途 |
| CA3228456A1 (en) * | 2021-12-13 | 2023-06-22 | Abbisko Therapeutics Co., Ltd. | Fgfr4 inhibitor acid salt, preparation method therefor and use thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6316466B1 (en) * | 1998-05-05 | 2001-11-13 | Syntex (U.S.A.) Llc | Pyrazole derivatives P-38 MAP kinase inhibitors |
| IL139169A0 (en) * | 1998-05-05 | 2001-11-25 | Hoffmann La Roche | Pyrazole derivatives as p-38 map kinase inhibitors |
| WO2005009973A1 (en) * | 2003-06-26 | 2005-02-03 | Novartis Ag | 5-membered heterocycle-based p38 kinase inhibitors |
| ES2383273T3 (es) * | 2008-07-23 | 2012-06-19 | F. Hoffmann-La Roche Ag | Compuestos heterocíclicos antivíricos |
-
2012
- 2012-02-07 JP JP2012023811A patent/JP5620417B2/ja not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3015953B1 (ja) | 1998-10-06 | 2000-03-06 | 株式会社ワールド・ブリック | れんが壁 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2012180344A (ja) | 2012-09-20 |
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