Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486464Generated: October 26, 2026

Ammonium Hydroxide → 3-(4-Ethylphenoxy)-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine

https://huagongshe.com/reaction/486464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1-(m-Tolyl)piperazineHCID 83111—
Reactant6-Chloro-3-(4-ethylphenoxy)pyridazineHCID 19095610—
SolventChloroformHCID 6212—
Product3-(4-Ethylphenoxy)-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazineHCID 1512460627%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4 parts of 6-chloro-3-(4-ethylphenoxy)pyridazine and 6 parts of 1-(3-methylphenyl)piperazine was stirred and heated for 3 hours in an oil bath at 110° C. The whole was allowed to stand overnight. Concentrate ammonium hydroxide and trichloromethane were added. The precipitate was filtered off and the filtrate was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.7 parts (27%) of 3-(4-ethylphenoxy)-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine; mp. 106.6° C. (compound 221).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-aa6beb77fb424c0f84415d8de8ef212e
Source noteuspto-grants-1994_03