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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3577생성일: 2026년 10월 24일

O-Toluidine → N-(2-Methylphenyl)-4-(5H-pyrrolo[2,1-c][1,4]-benzodiazepin-10(11H)-ylcarbonyl)benzamide

https://huagongshe.com/ko/reaction/3577

반응식

참여 물질

역할이름HCID투입량
반응물O-ToluidineHCID 7242—
반응물TriethylamineHCID 8471—
반응물4-(5H-pyrrolo[2,1-c]-[1,4]benzodiazepin-10(11H)-ylcarbonyl)benzoic acidHCID 9905628—
반응물DiethylphosphorylcyanideHCID 13586794—
용매DichloromethaneHCID 6344—
생성물N-(2-Methylphenyl)-4-(5H-pyrrolo[2,1-c][1,4]-benzodiazepin-10(11H)-ylcarbonyl)benzamideHCID 2183697354.6%

반응 단계

A mixture of 0.332 g of 4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)benzoic acid, 0.111 g of triethylamine, 0.107 g of o-toluidine, and 0.15 ml of diethylphosphoryl cyanide in 20 ml of dichloromethane is heated on a steam bath overnight. The mixture is washed with water, 1M NaHCO3, 1N HCl, brine and dried (Na2SO4). The dichloromethane solution is filtered through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness. The residue is crystallized from dichloromethane-hexane to give 0.23 g of white crystals, m.p. 228°-231° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733905
출처 데이터셋uspto-grants-1998_03
ORD IDord-4c868244e3744e8ba1d62fa5fdf18432
출처 메모uspto-grants-1998_03