Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192394Generated: November 2, 2026

Chloroacetyl chloride → HCID 67028039, compound

https://huagongshe.com/reaction/2192394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant2-Methylpyrimidin-4-amineHCID 295763—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67028039HCID 670280397.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-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 to give a solid that was filtered, 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 (70 mg, 7.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-0ff78507101f4f73b37b2d18b142515d
Source noteuspto-grants-2012_12