Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192396Generated: November 1, 2026

Chloroacetyl chloride → 2-Chloro-N-(6-methyl-pyrimidin-4-yl)-acetamide

https://huagongshe.com/reaction/2192396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant6-Methylpyrimidin-4-amineHCID 572852—
Solvent1,2-DichloroethaneHCID 11—
Product2-Chloro-N-(6-methyl-pyrimidin-4-yl)-acetamideHCID 67311001—

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Methyl-pyrimidin-4-yl amine (545 mg) was suspended in DCE (5 mL) and chloroacetylchloride (0.4 mL) was added dropwise. The reaction was heated in a microwave at 80° C. for 5 mins. The reaction mixture was cooled, filtered and a solid obtained. The reaction was repeated a second time and both batches of solid were combined, washed with dichloromethane then suspended in dichloromethane and sat. NaHCO3 (aq.) was added. The organic phase was collected and the aqueous layer extracted with dichloromethane (×2). The combined organic layer was dried over sodium sulphate and concentrated. The crude product was purified by silica gel chromatography eluting with 0-10% MeOH/dichloromethane to give the sub-titled compound as a yellow solid (120 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-1eb3fa1fdb7f40f680bbcd6ed7731817
Source noteuspto-grants-2012_12