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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233376생성일: 2026년 10월 25일

benzyl (2S)-2-aminopropanoate → N-[2-acetylthiomethyl-3-(4-hydroxyphenyl)-1-oxobutyl]alanine benzyl ester

https://huagongshe.com/reaction/233376

반응식

참여 물질

역할이름HCID투입량
반응물benzyl (2S)-2-aminopropanoateHCID 726858—
반응물2-Acetylthiomethyl-3-(4-hydroxyphenyl)butanoic acidHCID 18980788—
생성물N-[2-acetylthiomethyl-3-(4-hydroxyphenyl)-1-oxobutyl]alanine benzyl esterHCID 5441291869%

반응 단계

Using the procedure described in Example 60, but starting with 2-acetylthiomethyl-3-(4-hydroxyphenyl)butanoic acid and alanine benzyl ester, N-[2-acetylthiomethyl-3-(4-hydroxyphenyl)-1-oxobutyl]alanine benzyl ester is obtained in a 69% yield, the characteristics of which are as follows: Rf= 0.22 [hexane/ethyl acetate (65:35 by volume)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591891
출처 데이터셋uspto-grants-1997_01
ORD IDord-ba6031c10ed24dde85aae8303e12c2c9
출처 메모uspto-grants-1997_01