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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58703생성일: 2026년 10월 24일

Diisopropylethylamine → N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(3-ethylphenyl)-2-oxopyrrolidine-3-carboxamide

https://huagongshe.com/ko/reaction/58703

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
반응물1-(3-Ethylphenyl)-2-oxopyrrolidine-3-carboxylic acidHCID 24689356—
용매DimethylformamideHCID 6228—
생성물N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(3-ethylphenyl)-2-oxopyrrolidine-3-carboxamideHCID 4986890933.6%

반응 단계

A mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.099 g; 0.428 mmol), PyBOP (0.335 g; 0.643 mmol), N,N-diisopropylethylamine (0.222 mL; 1.29 mmol) and 1-(3-ethylphenyl)-2-oxopyrrolidine-3-carboxylic acid (0.100 g; 0.428 mmol) was stirred in DMF (3 mL) overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulfate, the organic layer was washed with sodium carbonate, brine, dried and concentrated under reduced pressure. The crude mixture was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.059 g (33%) of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434722B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ef562a0c2f7b444bb1b0ede4e7085866
출처 메모uspto-grants-2016_09