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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3555생성일: 2026년 10월 24일

Triethylamine → N-[4-[(6,7-Dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepin-5-yl)carbonyl)phenyl]-2-methylbenzamide

https://huagongshe.com/ko/reaction/3555

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
반응물6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepineHCID 12359341—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물N-[4-[(6,7-Dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepin-5-yl)carbonyl)phenyl]-2-methylbenzamideHCID 21837085—

반응 조건

온도0 °C

반응 단계

To a mixture of 1.37 g (5 mmol) of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 10 ml of methylene chloride, cooled to 0° C. is added 7 mmol of triethylamine and 5 mmol of 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepine. The cooling bath is removed and the reaction mixture is allowed to stir at room temperature for 48 hours. The volatiles are removed in vacuo to give a residue. The residue is dissolved in 100 ml of ethyl acetate and washed with water, 2N citric acid, aqueous NaHCO3 and brine. The solution is dried with Na2SO4 and the solvent removed in vacuo to give a solid. The solid is triturated with ether-hexane to give the desired product, mass spectrum (CI): 422(M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733905
출처 데이터셋uspto-grants-1998_03
ORD IDord-5681035ee10241e3b5bb6098bf1ffd50
출처 메모uspto-grants-1998_03