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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1420007생성일: 2026년 10월 25일

Triethylamine → N-[4-(4H-Pyrazolo[5,1-c][1,4]benzodiazepin-5(10H)-ylcarbonyl)phenyl]-2-methylbenzamide

https://huagongshe.com/reaction/1420007

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
반응물5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepineHCID 13062825—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물N-[4-(4H-Pyrazolo[5,1-c][1,4]benzodiazepin-5(10H)-ylcarbonyl)phenyl]-2-methylbenzamideHCID 21837012—

반응 조건

온도0 °C

반응 단계

To a mixture of 1.37 g of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 15 ml of methylene chloride, cooled to 0° C. is added 1.5 ml of triethylamine. To the mixture is added 5 mmol of 5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine. The reaction mixture is allowed to stir at room temperature for 48 hours and 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. The residue is purified by flash chromatography on silica gel with ethyl acetate-hexane to give the desired product, m.p. 142°-146° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05889001
출처 데이터셋uspto-grants-1999_03
ORD IDord-1a0ddebdadc74038afcae7ebff997bd4
출처 메모uspto-grants-1999_03