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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32828생성일: 2026년 10월 24일

Trifluoroacetic acid → (2S,3S)-2-(2-amino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/32828

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물2-((2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl esterHCID 86603389—
용매DichloromethaneHCID 6344—
생성물(2S,3S)-2-(2-amino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl esterHCID 8660339071.2%

반응 단계

2-((2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester (0.65 g, 1.54 mmol) was mixed in dichloromethane (5 mL) in an ice-bath. Trifluoroacetic acid (5 mL) was added and the solution was stirred for 2 hours. The reaction mixture was evaporated and the residue was precipitated with ether. The mixture was stirred vigorously for 10 minutes and then filtered. The solid was partitioned between aqueous sodium bicarbonate and dichloromethane. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with brine and dried (sodium sulfate). Evaporation of the solvents gave 2-((2S,3S)-2-amino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester (0.35 g, 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427635B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0d892e3e44a74ef9849795f2cc5c39e5
출처 메모uspto-grants-2008_09