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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127449생성일: 2026년 10월 24일

Water → N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/ko/reaction/127449

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Amino-4-methylpiperazineHCID 81349—
반응물7-Nitro-1,4-benzodioxane-5-carbonyl chlorideHCID 20544745—
용매Methyl Ethyl KetoneHCID 6569—
생성물N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamideHCID 2054469955.8%

반응 조건

온도10 °C

반응 단계

33 g of 1-amino-4-methylpiperazine were dissolved in 630 ml of methyl ethyl ketone. The mixture was cooled to 10° C. and 61 g of 7-nitro-1,4-benzodioxane-5-carbonyl chloride were introduced by portions. The mixture was stirred for two hours and then the solid was filtered off and washed with 150 ml of methyl ethyl ketone. The obtained product was purified by transformation into the base (M.P.: 212° C.) and recystallized by treatment with hydrochloric ethanol. 45 g of N-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamide were obtained (M.P.: 210° C. with one mole of water). The structure was confirmed by nuclear magnetic resonance and infrared analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255580
출처 데이터셋uspto-grants-1981_03
ORD IDord-15a0016f5e2a4643903fc71c61d06e76
출처 메모uspto-grants-1981_03