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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4175생성일: 2026년 10월 23일

Formaldehyde → 5,11-Dihydro-11-[1-oxo-2-methyl-6-(4-methyl-1-piperazinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

https://huagongshe.com/ko/reaction/4175

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물1-MethylpiperazineHCID 53167—
반응물Maleic AcidHCID 444266—
반응물5,11-Dihydro-11-[1-oxo-2-methyl-4-pentynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-oneHCID 13729207—
촉매Cuprous chlorideHCID 62652—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물5,11-Dihydro-11-[1-oxo-2-methyl-6-(4-methyl-1-piperazinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-oneHCID 13924396—

반응 단계

A reaction mixture consisting of 36.6 g (0.12 mol) of 5,11-dihydro-11-[1-oxo-2-methyl-4-pentynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one, 4 g (0.13 mol) of paraformaldehyde, 13.2 g (0.13 mol) of N-methylpiperazine, 0.2 g of copper(I) chloride and 600 ml of dioxan is refluxed for 2 hours. After the reaction has ended the mixture is filtered over activated charcoal to remove the insoluble components and the filtrate is evaporated to dryness in vacuo. In order to purify it, the crude product is suspended in a solution of 15.4 g (0.13 mol) of maleic acid in 600 ml of water and stirred for 1 hour at ambient temperature. The insoluble matter is filtered off, the filtrate is made alkaline by the addition of potassium carbonate and the resin precipitated is taken up in 600 ml of methylene chloride. After drying over magnesium sulphate, the solution is evaporated to dryness in vacuo. The crystalline residue is decocted with 150 ml of ethyl acetate and suction filtered after cooling. By digesting it in a little ethyl acetate a crystalline product is obtained which melts at 212° to 214° C. after washing with ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04724236
출처 데이터셋uspto-grants-1988_02
ORD IDord-6577de97230742bfbdfb63b5e64d45dc
출처 메모uspto-grants-1988_02