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HRID 20333作成日:2026年10月26日

Water → (R)-4-[(1S,2S)-2-Amino-3-(3,5-difluorophenyl)-1-hydroxypropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/20333

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物(R)-4-[(1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl esterHCID 58972248—
触媒Nickel DichlorideHCID 24385—
溶媒MethanolHCID 887—
生成物(R)-4-[(1S,2S)-2-Amino-3-(3,5-difluorophenyl)-1-hydroxypropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl esterHCID 6856229495%

反応手順

Combine (R)-4-[(1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester (1.13 g, 2.71 mmol) and nickel (II) chloride (0.58 g, 4.485 mmol) in dry methanol (30 ml) and add sodium borohydride (0.454 g, 12 mmol) over 1 minute. Stir the resulting mixture for 20 minutes and then add water (3 mL). Concentrate and dissolve the residue in ethyl acetate. Filter the black solution through a pad of Celite® and wash the filter cake with ethyl acetate. Wash the filtrate with water (twice), saturated aqueous sodium chloride, dry (magnesium sulfate), filter, and concentrate to give the desired compound as a white solid (920 mg, 95%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745438B2
出典データセットuspto-grants-2010_06
ORD IDord-cc02d55a1a304c93a1f76ea81947d101
出典メモuspto-grants-2010_06