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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715257Generated: November 3, 2026

Ethyl Bromide → HCID 86616231, compound

https://huagongshe.com/reaction/1715257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAcetonitrileHCID 6342—
Reactant5H,6H,7H,8H-imidazo(1,5-c)pyrimidin-5-oneHCID 1487518—
SolventDimethylformamideHCID 6228—
ProductHCID 86616231HCID 86616231—

Reaction Conditions

Temperature180 °C

Reaction Steps

A suspension of 7,8-dihydroimidazo[1,5-c]pyrimidin-5(6H)-one, obtained in step I as describe above (500 mg; 3.65 mmol; 1 eq), and bromoethane (816 μl; 10.94 mmol; 3 eq) in DMF (7 ml) is divided in two equals fractions and heated under microwave irradiation at 180° C. for 20 min. The reaction mixtures are combined and acetonitrile (15 ml) is added. The resulting precipitate is filtered, washed with acetonitrile and dried under vacuum, affording the title compound that is used in the next step without further purification (118.3 mg; 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799814B2
Source datasetuspto-grants-2010_09
ORD IDord-1f01aab1ff454ea1a442dcffa9b70849
Source noteuspto-grants-2010_09