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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279648Generated: October 30, 2026

2-(N-(3,6-dichloropyridazin-4-yl)-N-methylamino)ethanol → HCID 22030726, compound

https://huagongshe.com/reaction/279648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(N-(3,6-dichloropyridazin-4-yl)-N-methylamino)ethanolHCID 22030775—
CatalystPalladiumHCID 23938—
SolventAmmoniaHCID 222—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 22030726HCID 2203072691%

Reaction Steps

A mixture of 2-(N-(3,6-dichloropyridazin-4-yl)-N-methylamino)ethanol (444 mg, 2 mmol) and 10% palladium-on-charcoal catalyst (150 mg) in ethanol (15 ml), methanol (5 ml) and aqueous ammonia (15 ml) was stirred under hydrogen at 3 atmospheres pressure for 4 hours. The catalyst was removed by filtration and the solvent removed from the filtrate by evaporation. The residue was dissolved in methylene chloride, the insoluble material was removed by filtration and the solvent was removed from the filtrate by evaporation. The residue was purified by column chromatography on neutral aluminum oxide eluting with methylene chloride/methanol (95/5 followed by 90/10). The purified product was triturated with petroleum ether, the solid product was collected by filtration and dried under vacuum to give 2-(N-methyl-N-(pyridazin-4-yl)amino)ethanol (275 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362336B1
Source datasetuspto-grants-2002_03
ORD IDord-1f9829dd9f104eaeb09a9a814c00cb41
Source noteuspto-grants-2002_03