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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 439979생성일: 2026년 10월 25일

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/reaction/439979

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 toom 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 번호US05516774
출처 데이터셋uspto-grants-1996_05
ORD IDord-a3959319ba4843e7abacd76ad74523f1
출처 메모uspto-grants-1996_05