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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63716생성일: 2026년 10월 26일

2,6-Dichlorobenzoyl chloride → (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester

https://huagongshe.com/reaction/63716

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dichlorobenzoyl chlorideHCID 78392—
반응물DiisopropylethylamineHCID 81531—
반응물4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl esterHCID 11011855—
용매DichloromethaneHCID 6344—
생성물(S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl esterHCID 5439386188.5%

반응 단계

To a solution of (S)-3-[4-aminophenyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester (37.57 g, 127.6 mmol) and 2,6-dichlorobenzoyl chloride (29.45 g, 140.6 mmol) in dichloromethane (350 mL) was added DIPEA (24.8 g, 192 mmol) at room temperature. The brown solution was stirred for 15 h at room temperature to afford a white suspension at this time TLC analysis of the mixture indicated the absence of starting material. Then, the solids were collected by filtration and the solids were washed with dichloromethane (150 mL) and air dried to obtain 52.75 g (88.4% yield) of (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester as a white solid: mp 192-194° C. ES(+)-HRMS m/e calcd. for C22H24Cl2N2O5 (M+H)+ 466.1062, obsd. 466.1069.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447035B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ec259c0dcfa745ae80aa81e4c827b872
출처 메모uspto-grants-2016_09