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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3598생성일: 2026년 10월 23일

alpha-Bromo-o-chlorotoluene → N-[(2-Chlorophenyl)methyl]-N-[4-(5H-pyrrolo(2,1-c]-[1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl)-4-morpholineacetamide

https://huagongshe.com/ko/reaction/3598

반응식

참여 물질

역할이름HCID투입량
반응물alpha-Bromo-o-chlorotolueneHCID 11905—
반응물Sodium hydrideHCID 24758—
반응물N-[4-(5H-pyrrolo-[2,1-c][1,4]benzodiazepin10(11H)-ylcarbonyl)phenyl]4-morpholineacetamideHCID 70059534—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물N-[(2-Chlorophenyl)methyl]-N-[4-(5H-pyrrolo(2,1-c]-[1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl)-4-morpholineacetamideHCID 15340681126.9%

반응 단계

A mixture of 0.11 g of N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]-4-morpholineacetamide, 56 mg of O-chlorobenzyl bromide and 0.41 g of K2 CO3 in 5 ml of acetonitrile is heated at reflux for 18 hours. An additional 30 mg of O-chlorobenzyl bromide and 0.4 mmol of sodium hydride is added followed by heating for 24 hours. The reaction mixture is diluted with water and extracted with ethyl acetate. The organic layer is dried with Na2SO4 and evaporated to give 0.18 g of a residue which is purified by chromatography on silica gel with 1:1 ethyl acetate-methylene chloride to give 80 mg of off white solid. MS(CI): 555 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733905
출처 데이터셋uspto-grants-1998_03
ORD IDord-0377322d180742a7acad3e33e6f3f423
출처 메모uspto-grants-1998_03