Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 409034생성일: 2026년 10월 26일
Lithium borohydride → (5S,6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-ol
https://huagongshe.com/reaction/409034
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lithium borohydride | HCID 4148881 | — |
| 반응물 | (6S,9R)-6-(2,3-Difluorophenyl)-6,7,8,9-tetrahydro-9-[[tris(1-methylethyl)silyl]oxy]-5H-cyclohepta[b]pyridin-5-one | HCID 57911475 | — |
| 용매 | Cyclopentyl methyl ether | HCID 138539 | — |
| 생성물 | (5S,6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-ol | HCID 57911423 | 65% |
반응 단계
Lithium borohydride (0.982 g, 45.1 mmol) was added to a cyclopentyl methyl ether (30 mL) solution of (6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-one (5.0224 g, 11.27 mmol) at 0° C. under N2. The reaction mixture was stirred at 0° C. for 2 hours and then an addition 4 hours at room temperature. The reaction was quenched by adding methanol. The reaction mixture was stirred for 0.5 hour. The solvent was mostly removed via vacuum and the crude material was taken up in ethyl acetate, which was washed with water three times. Flash column by ethyl acetate in hexane from 0 to 10% gave the desired product (3.28 g, 65%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08759372B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-613adbb88c844232aca16582d503ae0a |
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| 출처 메모 | uspto-grants-2014_06 |
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