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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085797Generated: October 26, 2026

4-Methoxynaphthalen-1-ylmethylamine → 4,6-Dichloro-5-(4-methoxy-1-naphthylmethylamino)-3(2H)pyridazinone

https://huagongshe.com/reaction/1085797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxynaphthalen-1-ylmethylamineHCID 59139—
Reactant3,4,5-Trichlor-6-hydroxypyridazinHCID 11106349—
SolventEthanolHCID 702—
Product4,6-Dichloro-5-(4-methoxy-1-naphthylmethylamino)-3(2H)pyridazinoneHCID 9884758—

Reaction Steps

A mixture comprising 800 mg of 4,5,6-trichloro-3(2H)pyridazinone, 2.68 g of 4-methoxy-1-naphthylmethylamine and 10 ml of ethanol, was refluxed under stirring for 4 hours. After cooling, precipitated crystals were collected by filtration. Then, the product was dissolved in hot ethyl acetate and treated by silica gel. The filtrate was concentrated, and precipitated crystals were collected by filtration to obtain 330 mg of the above identified compound as colorless crystals having a melting point of from 228° to 231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011839
Source datasetuspto-grants-1991_04
ORD IDord-f83b4264c56b4aef9b9b6fb6f5dcebcc
Source noteuspto-grants-1991_04