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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351078Generated: November 3, 2026

Water → t-Butyl 4-[1-(2-butynyl)-7-oxo-6,7-dihydro-1H-imidazo[4,5-d]pyridazin-2-yl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1351078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Bromo-3-(but-2-ynyl)-3,5-dihydro-imidazo[4,5-d]pyridazin-4-oneHCID 21947658—
SolventDimethylformamideHCID 6228—
Productt-Butyl 4-[1-(2-butynyl)-7-oxo-6,7-dihydro-1H-imidazo[4,5-d]pyridazin-2-yl]piperazine-1-carboxylateHCID 21098100—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2.11 g of 2-bromo-3-(2-butyn-1-yl)-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one, 1.64 g potassium carbonate and 1.91 g 1-tert.-butyloxycarbonyl-piperazine in 20 ml N,N-dimethylformamide is stirred for six hours at 80° C. After cooling to ambient temperature the reaction mixture is combined with water and the precipitate formed is suction filtered. The crude product is purified by chromatography over a silica gel column with methylene chloride/methanol (95:5 to 90:10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217711B2
Source datasetuspto-grants-2007_05
ORD IDord-f5ee32ff804e47448d864314888c0ce2
Source noteuspto-grants-2007_05