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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454940Generated: October 26, 2026

Triethylamine → 1-(1-(3,6-Dichloropyridazin-4-yl)piperidin-4-yl)ethanone

https://huagongshe.com/reaction/454940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,4,6-TrichloropyridazineHCID 95123—
Reactant1-(Piperidin-4-yl)ethan-1-oneHCID 2723764—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(1-(3,6-Dichloropyridazin-4-yl)piperidin-4-yl)ethanoneHCID 5854795739%

Reaction Steps

Triethylamine (2.2 g, 20.0 mmol), 3,4,6-trichloro-pyridazine (1.8 g, 10.0 mmol) and 1-(piperidin-4-yl)ethanone (1.3 g, 10.0 mmol) was dissolved in DMF (20 mL) and the resulting mixture was stirred at room temperature overnight. The mixture was then diluted with water (50 mL) and extracted with EtOAc (2×50 mL). The combined organic extracts were combined and washed with water (20 mL) and brine (20 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (20% to 50% EtOAc in hexanes) to give 1-(1-(3,6-dichloropyridazin-4-yl)piperidin-4-yl)ethanone (1.0 g, 3.8 mmol, 39% yield) as white solid. ESI-MS (M+1): 274 calc. for C11H13ClN3O 273.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497265B2
Source datasetuspto-grants-2013_07
ORD IDord-9f93ca938d46472888460804cf7f0d07
Source noteuspto-grants-2013_07