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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660040Generated: October 25, 2026

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

https://huagongshe.com/reaction/1660040

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 recrystallized 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 numberUS04306072
Source datasetuspto-grants-1981_12
ORD IDord-6314867bea52488c908c16beaad34445
Source noteuspto-grants-1981_12