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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

반응식

참여 물질

역할이름HCID투입량
반응물Lithium borohydrideHCID 4148881—
반응물(6S,9R)-6-(2,3-Difluorophenyl)-6,7,8,9-tetrahydro-9-[[tris(1-methylethyl)silyl]oxy]-5H-cyclohepta[b]pyridin-5-oneHCID 57911475—
용매Cyclopentyl methyl etherHCID 138539—
생성물(5S,6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-olHCID 5791142365%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759372B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-613adbb88c844232aca16582d503ae0a
출처 메모uspto-grants-2014_06