Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60817생성일: 2026년 10월 24일
(Bis(2-methoxyethyl)amino)sulfur trifluoride → N-((5-fluoro-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide
https://huagongshe.com/ko/reaction/60817
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| 반응물 | N-((5-hydroxy-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide | HCID 71715162 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-((5-fluoro-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide | HCID 71715220 | — |
반응 단계
A solution of N-((5-hydroxy-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide (0.07 mmol, 0.036 g) in DCM (0.3 mL) was added to a mixture of bis(2-methoxyethyl)aminosulfur trifluoride (0.14 mmol, 0.027 mL) in DCM (0.2 mL) at −78° C. under argon. The resulting mixture was stirred at −78° C. for 1 h and at rt for another 1.5 h. The desired product was purified by preparative TLC to give N-((5-fluoro-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide with unidentified stereochemistry (Y: 16%). MS (ESI) 489 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09440982B2 |
|---|
| 출처 데이터셋 | uspto-grants-2016_09 |
|---|
| ORD ID | ord-5080850ddb214b1684fe9feaad436637 |
|---|
| 출처 메모 | uspto-grants-2016_09 |
|---|