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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(N-(3,6-dichloropyridazin-4-yl)-N-methylamino)ethanol | HCID 22030775 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22030726 | HCID 22030726 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06362336B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-1f9829dd9f104eaeb09a9a814c00cb41 |
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| Source note | uspto-grants-2002_03 |
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