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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3532생성일: 2026년 10월 24일

Triethylamine → N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamide

https://huagongshe.com/ko/reaction/3532

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
반응물9,10-Dihydro-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepineHCID 21836966—
용매DichloromethaneHCID 6344—
생성물N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamideHCID 21837211—

반응 조건

온도0 °C

반응 단계

To a mixture of 1.1 mmol of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 10 ml of methylene chloride, cooled to 0° C. is added 1.5 mmol of triethylamine. To the mixture is added 1 mmol of 9,10-dihydro-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine and the mixture stirred at room temperature for 2 hours. The reaction mixture is concentrated in vacuo and 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 volatiles concentrated in vacuo to give a solid which is purified by flash chromatography to give the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733905
출처 데이터셋uspto-grants-1998_03
ORD IDord-5f938858357146d8a8d932bcaf02b969
출처 메모uspto-grants-1998_03