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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031428Generated: October 31, 2026

Ammonia → 6-(4-amino-3-nitrophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-one

https://huagongshe.com/reaction/1031428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant6-(4-chloro-3-nitrophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-oneHCID 2874432—
SolventEthanolHCID 702—
Product6-(4-amino-3-nitrophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-oneHCID 3111187—

Reaction Steps

A mixture of 5 g of 6-(4-chloro-3-nitrophenyl)-5-methyl-2,3,4,5-tetrahydropyridazin-3-one, 50 ml of 25% aqueous NH3 solution and 50 ml of ethanol is heated at 100° for 16 hours. The mixture is poured into ice water and extracted with methylene dichloride, the phases are separated and the organic phase is dried over sodium sulfate and evaporated to give 6-(4-amino-3-nitrophenyl)-5-methyl-2,3,4,5-tetrahydropyridazin-3-one, m.p. 234°-238°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954499
Source datasetuspto-grants-1990_09
ORD IDord-80a9b51fb2b5469085bb28abf00d12d2
Source noteuspto-grants-1990_09