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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73909생성일: 2026년 10월 25일

Triethylamine → {[2-(Tert-butoxycarbonyl-methyl-amino)acetyl]-methyl-amino}-acetic acid ethyl ester

https://huagongshe.com/reaction/73909

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Isobutyl chloroformateHCID 62365—
반응물Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
반응물Ethyl N-methylaminoacetate hydrochlorideHCID 171173—
용매DichloromethaneHCID 6344—
생성물{[2-(Tert-butoxycarbonyl-methyl-amino)acetyl]-methyl-amino}-acetic acid ethyl esterHCID 57470192—

반응 단계

To a stirred solution of (tert-butoxycarbonyl-methyl-amino)-acetic acid (37 g, 0.2 mol) and Et3N (60.6 g, 0.6 mol) in CH2Cl2 (300 mL) was added isobutyl chloroformate (27.3 g, 0.2 mmol) dropwise at −20° C. under argon. After stirring for 0.5 h, methylamino-acetic acid ethyl ester hydrochloride (30.5 g, 129 mmol) was added dropwise at −20° C. The mixture was allowed to warm to room temperature (c.a. 1 h) and quenched with water (500 mL). The organic layer was separated, washed with 10% citric acid solution, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (petroleum ether/EtOAc 1:1) to give {[2-(tert-butoxycarbonyl-methyl-amino)-acetyl]-methyl-amino}-acetic acid ethyl ester (12.5 g, 22

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829204B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4f98014265354558a01cdb1b0fffcff1
출처 메모uspto-grants-2014_09