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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127449Generated: October 26, 2026

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

https://huagongshe.com/reaction/127449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Amino-4-methylpiperazineHCID 81349—
Reactant7-Nitro-1,4-benzodioxane-5-carbonyl chlorideHCID 20544745—
SolventMethyl Ethyl KetoneHCID 6569—
ProductN-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamideHCID 2054469955.8%

Reaction Conditions

Temperature10 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255580
Source datasetuspto-grants-1981_03
ORD IDord-15a0016f5e2a4643903fc71c61d06e76
Source noteuspto-grants-1981_03