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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20392생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/20392

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium borohydrideHCID 4311764—
반응물(R)-5-[(1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl esterHCID 68564103—
촉매Nickel DichlorideHCID 24385—
용매MethanolHCID 887—
생성물(R)-5-[(1S,2S)-2-Amino-3-(3,5-difluorophenyl)-1-hydroxypropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl esterHCID 68563667—

반응 단계

To a solution of (R)-5-[(1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl ester (0.145 g, 0.325 mmol) in methanol (5 mL) at room temperature add nickel (II) chloride (0.063 g, 0.487 mmol) and then sodium borohydride (0.061 g, 1.62 mmol) portionwise. Stir 30 minutes, add water (˜3 mL) and concentrate. Dilute with ethyl acetate and filter through Celite®. Partition the filtrate between ethyl acetate and water. Dry the ethyl acetate layer (magnesium sulfate), filter and concentrate to give the desired compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745438B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c6d13efcbadb45c496155abf183d442b
출처 메모uspto-grants-2010_06