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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530870Generated: November 4, 2026

Pyridine → HCID 22398447, compound

https://huagongshe.com/reaction/1530870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 486363HCID 486363—
SolventDichloromethaneHCID 6344—
ProductHCID 22398447HCID 2239844736.5%

Reaction Steps

Pyridine (1 ml) was added to a mixture of 4-[[4-amino-6-[(2,6-dichloro-phenyl)methyl]-2-pyrimidinyl]amino]benzonitrile (0.00135 mol) in CH2Cl2 (19 ml). A solution of chloroethanoyl chloride (0.001375 mol) in CH2Cl2 (0.5 ml) was added dropwise on an ice bath. The mixture was stirred at room temperature for 2 hours. More chloroethanoyl chloride (0.00625 mol) in CH2Cl2 (0.5 ml) was added. The mixture stood in the refrigerator overnight. The solvent was evaporated. The residue was treated with a saturated Na2CO3 solution and the mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered and concentrated. The residue was purified by flash column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 99/1/0.1). The desired fractions were collected and the solvent was evaporated, yielding 0.22 g (36.5%) of 2-chloro-N-[6-[(2,6-dichloro-phenyl)methyl]-2-[(4-cyano-phenyl)amino]-4-pyrimidinyl]acetamide (interm. 13).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197779B1
Source datasetuspto-grants-2001_03
ORD IDord-dd08b6e5b9be4a248d02b41c139375b4
Source noteuspto-grants-2001_03