Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1413187Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1413187

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Amino-4-methylpiperazineHCID 81349—
Edukt7-Nitro-1,4-benzodioxane-5-carbonyl chlorideHCID 20544745—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
ProduktN-(4-methyl-1-piperazinyl)-7-nitro-1,4-benzodioxane-5-carboxamideHCID 2054469955,8%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

33 g of 1-amino-4-methylpiperazine was 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04248885
Quelldatensatzuspto-grants-1981_02
ORD IDord-16d62f90cac34b1992011eb98908c469
Quellennotizuspto-grants-1981_02