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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380678생성일: 2026년 10월 27일

Ethyl Acetate → 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propane

https://huagongshe.com/reaction/380678

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Bromoacetyl bromideHCID 61147—
반응물DiisopropylethylamineHCID 81531—
반응물2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 22508955—
용매TetrahydrofuranHCID 8028—
생성물2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 69736949—

반응 단계

To a stirring solution of 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane (7.51 g, 21.369 mmoles) in anhydrous tetrahydrofuran (100 ml) under a nitrogen atmosphere at 0° C. was added diisopropylethylamine (4.1 ml, 23.537 mmoles) and bromoacetyl bromide (2.05 ml, 23.530 mmoles). After 2 hours, ethyl acetate was added and the reaction mixture washed with water twice, 1.0 N hydrochloric acid (2×), saturated sodium bicarbonate solution (2×), and brine. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to a tan foam on a rotary evaporator. In this manner the 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propane was obtained in quantitative yield. No further purification was necessary.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06303610B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-c81ef57cd7754201a2b5e165da8f1a09
출처 메모uspto-grants-2001_10