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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070947Generated: October 31, 2026

Pyridine → HCID 488732, compound

https://huagongshe.com/reaction/1070947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOctanoyl chlorideHCID 8124—
ReactantHCID 486363HCID 486363—
SolventDichloromethaneHCID 6344—
ProductHCID 488732HCID 48873268.6%

Reaction Steps

Pyridine (0.014 mol) was added to a mixture of 4-[[4-amino-6-[(2,6-dichlorophenyl)-methyl]-2-pyrimidinyl]amino]benzonitrile (0.0013 mol) in CH2Cl2. A solution of octanoyl chloride (1.5 equiv) in CH2Cl2 (0.5 ml) was added dropwise. The mixture was stirred at room temperature for 2 hours. More octanoyl chloride (3,5 equiv) in CH2Cl2 was added dropwise. The mixture was stirred. The solvent was then evaporated. The residue was treated with a saturated aqueous NaHCO3 solution and the mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered and the solvent was evaporated to give the crude product. The residue was recrystallized from CHCl3 and hexane, yielding 0.443 g (68.6%) of N-[6-[(2,6-dichloro-phenyl)methyl]-2-[(4-cyano-phenyl)amino]-4-pyrimidinyl]octanamide (comp. 17; mp. 135-137° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903213B2
Source datasetuspto-grants-2005_06
ORD IDord-570e5ab538194ccf85a48846862ed393
Source noteuspto-grants-2005_06