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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1902488생성일: 2026년 10월 27일

1-Methylpiperazine → 1,3-Dimethyl-4-[3-(4-methyl-1-piperazinyl)propionyl]-1,4,9,10-tetrahydropyrrolo[3,2-b][1,5]benzodiazepin-10-one

https://huagongshe.com/reaction/1902488

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물4-(3-Bromopropionyl)-1,3-dimethyl-1,4,9,10-tetrahydropyrrolo[3,2-b][1,5]benzodiazepin-10-oneHCID 20515487—
용매1,4-DioxaneHCID 31275—
생성물1,3-Dimethyl-4-[3-(4-methyl-1-piperazinyl)propionyl]-1,4,9,10-tetrahydropyrrolo[3,2-b][1,5]benzodiazepin-10-oneHCID 2051544676%

반응 단계

1.5 g of 4-(3-bromopropionyl)-1,3-dimethyl-1,4,9,10-tetrahydropyrrolo[3,2-b][1,5]benzodiazepin-10-one and 0.85 g of N-methylpiperazine are warmed at 80° C. for 15 hours in 50 ml of dioxane. The thus-obtained mixture is concentrated to dryness in vacuo. 20 ml of saturated aqueous sodium carbonate solution are added thereto with stirring, and the mixture is then extracted three times with ethyl acetate. The combined extracts are dried over sodium sulfate, and the solvent is stripped off in vacuo. The resulting residue is chromatographed on neutral silica gel (methylene chloride/methanol 95/05). 1.2 g of the title compound of m.p. 187° C. (from isopropanol) are obtained).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04363816
출처 데이터셋uspto-grants-1982_12
ORD IDord-5438a24a039444bb838c30312aec8c6f
출처 메모uspto-grants-1982_12