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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3591생성일: 2026년 10월 23일

Triethylamine → alpha-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4)benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide

https://huagongshe.com/ko/reaction/3591

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Chloro(phenyl)acetyl chlorideHCID 102902—
반응물10,11-dihydro-10(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 10828280—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물alpha-Chloro-N-[4-(5H-pyrrolo[2,1-c][1,4)benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamideHCID 21837022106.9%

반응 단계

To a solution of 0.61 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 8 ml of methylene chloride is added 0.30 g of triethylamine followed by 0.47 g of (±)-2-chloro-2-phenylacetyl chloride in 2 ml of methylene chloride. The mixture is stirred at room temperature for 1 hour and then diluted with 10 ml of 50% NaHCO3. The methylene chloride is evaporated and the residue is extracted with ethyl acetate. The separated organic layer is washed with saturated NaHCO3 and brine and then dried with Na2SO4 followed by filtering through a pad of hydrous magnesium silicate. The filtrate is evaporated to a residue which is stirred with ether-hexane to give 0.98 g of pink solid. MS(CI): 456(M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733905
출처 데이터셋uspto-grants-1998_03
ORD IDord-e1104a14670241aeb4e8e0077b154812
출처 메모uspto-grants-1998_03