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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192344Generated: October 31, 2026

Chloroacetyl chloride → HCID 67030278, compound

https://huagongshe.com/reaction/2192344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant4-AminopyrimidineHCID 68958—
SolventChloroformHCID 6212—
ProductHCID 67030278HCID 6703027864.1%

Reaction Steps

A solution of chloroacetyl chloride (1.22 mmol) in anhydrous CHCl3 (2.4 mL) was added slowly to a mixture of 4-aminopyrimidine (1.11 mmol) and Et3N (1.66 mmol) in anhydrous CHCl3 (22 mL) at room temperature. The bright yellow mixture gradually turned orange and after 4 hr the reaction was quenched with H2O (1 mL). After stirring for 15 min the mixture was concentrated to dryness under reduced pressure and the residue purified by flash silica gel chromatography (1-2% MeOH/dichloromethane) to give a yellow solid (122 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-04276d6070f2444ea56ab3ca172f0c65
Source noteuspto-grants-2012_12