KR20190078646A - 디아실글리세리드 o-아실트랜스퍼라제 2의 억제제로서 유용한 인다졸 유도체 - Google Patents
디아실글리세리드 o-아실트랜스퍼라제 2의 억제제로서 유용한 인다졸 유도체 Download PDFInfo
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- KR20190078646A KR20190078646A KR1020197016983A KR20197016983A KR20190078646A KR 20190078646 A KR20190078646 A KR 20190078646A KR 1020197016983 A KR1020197016983 A KR 1020197016983A KR 20197016983 A KR20197016983 A KR 20197016983A KR 20190078646 A KR20190078646 A KR 20190078646A
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- Prior art keywords
- alkyl
- fluorophenyl
- chlorophenyl
- synthesis
- carboxamide
- Prior art date
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- 0 *C(CC1)C(*)CC1N Chemical compound *C(CC1)C(*)CC1N 0.000 description 10
- RUNMOKYIEKSZLC-SSDOTTSWSA-N CC(C[C@@H](C=C1)C#N)=C1Cl Chemical compound CC(C[C@@H](C=C1)C#N)=C1Cl RUNMOKYIEKSZLC-SSDOTTSWSA-N 0.000 description 1
- OHGBOTNTMIPYQZ-UHFFFAOYSA-N CC1C(N)=CC(C)=CC1N Chemical compound CC1C(N)=CC(C)=CC1N OHGBOTNTMIPYQZ-UHFFFAOYSA-N 0.000 description 1
- RJODRTKGBLPDOW-UHFFFAOYSA-N CC1C=CC(C(C)=C)=CC1 Chemical compound CC1C=CC(C(C)=C)=CC1 RJODRTKGBLPDOW-UHFFFAOYSA-N 0.000 description 1
- LLAMGYUWYUMHCH-UHFFFAOYSA-N CNc(cc1)ccc1C(OC)=O Chemical compound CNc(cc1)ccc1C(OC)=O LLAMGYUWYUMHCH-UHFFFAOYSA-N 0.000 description 1
- CTBHHUVNJWYUBF-RXMQYKEDSA-N N[C@@H](C=C1)NC=C1Cl Chemical compound N[C@@H](C=C1)NC=C1Cl CTBHHUVNJWYUBF-RXMQYKEDSA-N 0.000 description 1
Classifications
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- C07D515/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, 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
- C07D515/08—Bridged systems
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—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
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
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- 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
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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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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- C07D417/00—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
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- Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
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- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662424066P | 2016-11-18 | 2016-11-18 | |
| US62/424,066 | 2016-11-18 | ||
| PCT/US2017/061223 WO2018093696A1 (en) | 2016-11-18 | 2017-11-13 | Indazole derivatives useful as inhibitors of diacylglyceride o-acyltransferase 2 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20190078646A true KR20190078646A (ko) | 2019-07-04 |
Family
ID=62145755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020197016983A Withdrawn KR20190078646A (ko) | 2016-11-18 | 2017-11-13 | 디아실글리세리드 o-아실트랜스퍼라제 2의 억제제로서 유용한 인다졸 유도체 |
Country Status (12)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MA41179A (fr) | 2014-12-19 | 2017-10-24 | Cancer Research Tech Ltd | Composés inhibiteurs de parg |
| US20230174521A1 (en) | 2020-05-18 | 2023-06-08 | Merck Sharp & Dohme Llc | Novel diacylglyceride o-acyltransferase 2 inhibitors |
| AU2021356589A1 (en) * | 2020-10-08 | 2023-05-25 | Merck Sharp & Dohme Llc | Preparation of benzimidazolone derivatives as novel diacylglyceride o-acyltransferase 2 inhibitors |
| KR102993831B1 (ko) * | 2020-10-08 | 2026-07-23 | 머크 샤프 앤드 돔 엘엘씨 | 신규 디아실글리세리드 o-아실트랜스퍼라제 2 억제제로서의 옥스인돌 유도체의 제조 |
| US20240066027A1 (en) * | 2020-12-03 | 2024-02-29 | Domain Therapeutics | Novel par-2 inhibitors |
| AU2021409234A1 (en) * | 2020-12-22 | 2023-06-29 | Merck Sharp & Dohme Llc | Preparation of tetrahydroindazole derivatives as novel diacylglyceride o-acyltransferase 2 inhibitors |
| PL4496795T3 (pl) | 2022-03-23 | 2026-07-20 | Ideaya Biosciences, Inc. | Związki indazolowe podstawione piperazyną jako inhibitory parg |
| JP2025537517A (ja) * | 2022-11-01 | 2025-11-18 | メルク・シャープ・アンド・ドーム・エルエルシー | 新規ジアシルグリセリドo-アシルトランスフェラーゼ2阻害薬としてのピラゾロピリジン誘導体及びトリアゾロピリジン誘導体の調製 |
| AU2023400409A1 (en) | 2022-12-02 | 2025-06-26 | Merck Sharp & Dohme Llc | Preparation of fused azole derivatives as novel diacylglyceride o-acyltransferase 2 inhibitors |
| WO2025247370A1 (zh) * | 2024-06-01 | 2025-12-04 | 中国药科大学 | 双环类化合物及其医药用途 |
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| KR100338610B1 (ko) * | 1996-09-04 | 2002-05-27 | 디. 제이. 우드, 스피겔 알렌 제이 | 인다졸 유도체 및 포스포디에스터라제 (pde) 유형 iv 및 종양괴사인자 (tnf) 생산의 억제제로서 그의 용도 |
| DE69819311T2 (de) | 1997-03-07 | 2004-07-29 | Metabasis Therapeutics Inc., San Diego | Neue benzimidazol inhibitoren der fructose-1,6-bisphosphatase |
| AU6691798A (en) | 1997-03-07 | 1998-09-22 | Metabasis Therapeutics, Inc. | Novel indole and azaindole inhibitors of fructose-1,6-bisphosphatase |
| WO1998039344A1 (en) | 1997-03-07 | 1998-09-11 | Metabasis Therapeutics, Inc. | Novel purine inhibitors of fructose-1,6-bisphosphatase |
| CZ297264B6 (cs) | 1998-09-09 | 2006-10-11 | Metabasis Therapeutics, Inc. | Nové heteroaromatické inhibitory fruktóza-1,6-bisfosfatázy |
| CA2415742A1 (en) | 2000-07-25 | 2002-01-31 | Merck & Co., Inc. | N-substituted indoles useful in the treatment of diabetes |
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| MXPA04004982A (es) * | 2001-11-27 | 2004-08-11 | Hoffmann La Roche | Derivados de benzotiazol. |
| AR040241A1 (es) | 2002-06-10 | 2005-03-23 | Merck & Co Inc | Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia |
| CA2495943C (en) | 2002-08-29 | 2009-07-21 | Merck & Co., Inc. | Indoles having anti-diabetic activity |
| WO2004019869A2 (en) | 2002-08-29 | 2004-03-11 | Merck & Co., Inc. | Indoles having anti-diabetic activity |
| CA2512879A1 (en) | 2003-01-17 | 2004-08-12 | Soumya P. Sahoo | N-cyclohexylaminocarbonyl benzenesulfonamide derivatives |
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| US10568876B2 (en) | 2014-09-05 | 2020-02-25 | Merck Sharp & Dohme Corp. | Tetrahydroisoquinoline derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2 |
| EP3188730B1 (en) * | 2014-09-05 | 2019-05-01 | Merck Sharp & Dohme Corp. | Tetrahydroisoquinoline derivatives useful as inhibitors of diacylglyceride o-acyltransferase 2 |
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2017
- 2017-11-13 RU RU2019117556A patent/RU2019117556A/ru unknown
- 2017-11-13 CA CA3043203A patent/CA3043203A1/en not_active Abandoned
- 2017-11-13 AU AU2017360939A patent/AU2017360939B2/en not_active Expired - Fee Related
- 2017-11-13 EP EP17871593.4A patent/EP3541374B1/en active Active
- 2017-11-13 US US16/461,902 patent/US11104690B2/en active Active
- 2017-11-13 JP JP2019526217A patent/JP2020502058A/ja not_active Ceased
- 2017-11-13 MX MX2019005786A patent/MX2019005786A/es unknown
- 2017-11-13 WO PCT/US2017/061223 patent/WO2018093696A1/en not_active Ceased
- 2017-11-13 BR BR112019010164-0A patent/BR112019010164A2/pt not_active IP Right Cessation
- 2017-11-13 MA MA046856A patent/MA46856A/fr unknown
- 2017-11-13 KR KR1020197016983A patent/KR20190078646A/ko not_active Withdrawn
- 2017-11-13 CN CN201780071343.9A patent/CN110121341A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP3541374A1 (en) | 2019-09-25 |
| AU2017360939B2 (en) | 2022-03-03 |
| AU2017360939A1 (en) | 2019-05-16 |
| CN110121341A (zh) | 2019-08-13 |
| MA46856A (fr) | 2019-09-25 |
| CA3043203A1 (en) | 2018-05-24 |
| BR112019010164A2 (pt) | 2019-09-17 |
| US11104690B2 (en) | 2021-08-31 |
| RU2019117556A (ru) | 2020-12-18 |
| EP3541374A4 (en) | 2020-06-10 |
| US20190330239A1 (en) | 2019-10-31 |
| JP2020502058A (ja) | 2020-01-23 |
| WO2018093696A1 (en) | 2018-05-24 |
| MX2019005786A (es) | 2019-08-26 |
| RU2019117556A3 (cg-RX-API-DMAC10.html) | 2020-12-18 |
| EP3541374B1 (en) | 2026-08-05 |
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