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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27896Generated: October 25, 2026

Ethanol → 3-(1-Methylhydrazino)-6-(3,5-dimethyl-1-pyrazolyl)-pyridazine

https://huagongshe.com/reaction/27896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethylhydrazineHCID 6061—
Reactant3-Chloro-6-(3,5-dimethylpyrazol-1-yl)pyridazineHCID 321073—
SolventWaterHCID 962—
Product3-(1-Methylhydrazino)-6-(3,5-dimethyl-1-pyrazolyl)-pyridazineHCID 12562864—

Reaction Steps

A mixture of 4.17 g (0.02 moles) of 3-chloro-6-(3,5-dimethyl-1-pyrazolyl)-pyridazine, 42 ml of ethanol and 2.3 g (0.05 moles) of methyl hydrazine is heated to reflux for 9 hours, and after cooling the mixture is poured into 100 ml of water. The solution is extracted with 3×50 ml of chloroform and the combined organic phases are dried over magnesium sulphate. After evaporation the residue is recrystallized from a 3:1 mixture of isopropanol and petroleum ether. Yield: 1.9 g (44.5%); m.p.: 93°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224325
Source datasetuspto-grants-1980_09
ORD IDord-8f3ad70dcc0149729543ac45493e93d6
Source noteuspto-grants-1980_09