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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297601Generated: October 30, 2026

Pyridine → HCID 18382492, compound

https://huagongshe.com/reaction/2297601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 18382510HCID 18382510—
SolventDichloromethaneHCID 6344—
ProductHCID 18382492HCID 18382492—

Reaction Steps

0.5 g of 2-aminomethyl-6-benzyl-7-cyclopentyl-4-ethyl-imidazo[4.5-e]-s-triazolo[1.5-a]pyrimidin-5-one (for preparation see synthesis example II) are dissolved in 10 ml of dichloromethane and 0.2 ml of pyridine, and 0.1 ml of acetyl chloride is added dropwise whilst cooling. After 2 hours' stirring at constant temperature the mixture is diluted with 10 ml of dichloromethane for working up and washed twice with dilute aqueous hydrochloric acid. The organic phase is separated off, dried over magnesium sulphate and the solvent is distilled off in vacuo. 0.7 g of the title compound are left in the form of an amorphous colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492377B1
Source datasetuspto-grants-2002_12
ORD IDord-216ed1c4ad474f068d2841863c16fc6a
Source noteuspto-grants-2002_12