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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20353생성일: 2026년 10월 23일

Butyl bromide → 5-(R)-[2-(S)-Acetylamino-3-(3-butoxyphenyl)-1-(S)-hydroxypropyl]-2-(R)-(2,2-dimethylpropoxy)-3-(S)-methylmorpholine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/20353

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참여 물질

역할이름HCID투입량
반응물Butyl bromideHCID 8002—
반응물Cesium carbonateHCID 10796—
반응물5-[2-(S)-Acetylamino-1-(S)-hydroxy-3-(3-hydroxyphenyl)-propyl]-2-(R)-(2,2-dimethylpropoxy)-3-(S)-methylmorpholine-4-carboxylic acid tert-butyl esterHCID 68563624—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-(R)-[2-(S)-Acetylamino-3-(3-butoxyphenyl)-1-(S)-hydroxypropyl]-2-(R)-(2,2-dimethylpropoxy)-3-(S)-methylmorpholine-4-carboxylic acid tert-butyl esterHCID 58972241102.5%

반응 조건

온도60 °C

반응 단계

Add 1-bromobutane (6 μL, 55.6 μmol) to a solution of 5-[2-(S)-acetylamino-1-(S)-hydroxy-3-(3-hydroxyphenyl)-propyl]-2-(R)-(2,2-dimethylpropoxy)-3-(S)-methylmorpholine-4-carboxylic acid tert-butyl ester (25 mg, 50.5 μmol) and cesium carbonate (33 mg, 1.01 mmol) in N,N-dimethylformamide (250 μL). Heat to 60° C. for 3 hours. Dilute with ethyl acetate, wash with water, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 20:80 to 85:15 ethyl acetate:dichloromethane) to give the title compound (28.5 mg, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745438B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-09d161281e8047b8a1ed6073750586a1
출처 메모uspto-grants-2010_06