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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294415Generated: October 30, 2026

Pyridine → HCID 22398447, compound

https://huagongshe.com/reaction/1294415

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 mol) 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 numberUS07241458B1
Source datasetuspto-grants-2007_07
ORD IDord-5561f6c34355460c85b1563a2464ad3c
Source noteuspto-grants-2007_07