돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 649263생성일: 2026년 10월 24일

Nitromethane → 7-Chloro-1,3-dihydro-2-nitromethylene-5-phenyl-2H-1,4-benzodiazepine

https://huagongshe.com/ko/reaction/649263

반응식

참여 물질

역할이름HCID투입량
반응물NitromethaneHCID 6375—
반응물Sodium hydrideHCID 24758—
반응물HydrideHCID 166653—
반응물7-chloro-2-di-(morpholino)phosphinyloxy-5-phenyl-3H-1,4-benzodiazepinHCID 14907886—
용매DimethylformamideHCID 6228—
생성물7-Chloro-1,3-dihydro-2-nitromethylene-5-phenyl-2H-1,4-benzodiazepineHCID 70053732—

반응 단계

To a mixture of 1.0 ml. of nitromethane and 5 ml. of dry dimethylformamide was added 53 mg. of a 50% dispersion of sodium hydride in mineral oil (1.1 mmole hydride). After 1 hour at room temperature, under nitrogen, 489 mg. (1.0 mmole) of 7-chloro-2-di-(morpholino)phosphinyloxy-5-phenyl-3H-1,4-benzodiazepine was added. After stirring at room temperature for 2 hours, dimethylformamide was evaporated (about 80°). The residue was partitioned between methylene chloride and an aqueous layer which is acidified with a slight excess of acetic acid. The methylene chloride layer was dried (Na2SO4) and evaporated. Separation of the product mixture by preparative tlc (silica gel, developed in 10% methanol in ethylacetate v/v) afforded pure final product, which upon crystallization from methanol, had a m.p. of 178°-180°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04739049
출처 데이터셋uspto-grants-1988_04
ORD IDord-e23de29fe43843a3aa50a16921825b2f
출처 메모uspto-grants-1988_04