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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55138생성일: 2026년 10월 24일

Triethylamine → N-[4-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]-2-methoxybenzamide

https://huagongshe.com/ko/reaction/55138

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Methoxybenzoyl chlorideHCID 88969—
반응물10,11-dihydro-10(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 10828280—
용매DichloromethaneHCID 6344—
생성물N-[4-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]-2-methoxybenzamideHCID 1078911759.6%

반응 단계

To a stirred solution of 0.362 g of 2-methoxybenzoyl chloride 5 ml of methylene chloride is added 0.346 g of triethylamine at 0° C. After stirring for 3 minutes, 0.500 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine is added and stirring continued for 18 hours at room temperature. The reaction mixture is diluted with 45 ml of methylene chloride and washed with water, 2N citric acid, 1M NaHCO3, and brine. The reaction mixture is dried with Na2SO4, filtered through hydrous magnesium silicate and evaporated in vacuo to give a solid which is purified by crystallization from ethyl acetate to give 0.430 g of the desired product as a crystalline solid, m.p. 185°-188° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624923
출처 데이터셋uspto-grants-1997_04
ORD IDord-e81c778e12ec40c4bb6c28cb5dd723a3
출처 메모uspto-grants-1997_04