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HRID 409034作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium borohydrideHCID 4148881—
反応物(6S,9R)-6-(2,3-Difluorophenyl)-6,7,8,9-tetrahydro-9-[[tris(1-methylethyl)silyl]oxy]-5H-cyclohepta[b]pyridin-5-oneHCID 57911475—
溶媒Cyclopentyl methyl etherHCID 138539—
生成物(5S,6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-olHCID 5791142365%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759372B2
出典データセットuspto-grants-2014_06
ORD IDord-613adbb88c844232aca16582d503ae0a
出典メモuspto-grants-2014_06