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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297598Generated: October 30, 2026

Triethylamine → HCID 15432862, compound

https://huagongshe.com/reaction/2297598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl bromideHCID 68176—
ReactantHCID 15432861HCID 15432861—
SolventDichloromethaneHCID 6344—
ProductHCID 15432862HCID 15432862—

Reaction Steps

0.6 g of 6-benzyl-7-cyclopentyl-4-ethyl-2-hydroxymethyl-imidazo[4,5-e]-s-triazolo[1,5-a]pyrimidin-5-one are taken up in 7 ml of dichloromethane and 0.25 ml of triethylamine are added at ambient temperature with stirring. Then 0.15 ml of thionyl bromide are added. After 2 hours' stirring at constant temperature the reaction is complete. For working up, the mixture is diluted with 20 ml of dichloromethane and washed successively with 15 ml of water and 15 ml of aqueous sodium chloride solution. The organic phase is dried over magnesium sulphate and the solvent is distilled off in vacuo. The residue remaining is recrystallised from diethyl ether. 0.45 g of the title compound remain, pure enough to be used in the subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492377B1
Source datasetuspto-grants-2002_12
ORD IDord-b3b06a44a3a842d48d9515ac57abfcd0
Source noteuspto-grants-2002_12