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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373964Generated: October 31, 2026

6-Butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine → 6-Butyl-5-(4-iodobenzyl)-2-methylpyrimidine-4-carbonitrile

https://huagongshe.com/reaction/373964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidineHCID 19018796—
ReactantHCID 178418546HCID 178418546—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product6-Butyl-5-(4-iodobenzyl)-2-methylpyrimidine-4-carbonitrileHCID 1901880087.5%

Reaction Steps

A mixture of 800 mg (8.94 mmol) CuCN and 10 mL pyridine was heated to 110° C. until all of the CuCN went into solution (7 minutes). To this mixture was added a solution of 440 mg (0.894 mmol) 6-butyl-4-iodo-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine in 3 mL pyridine. After 5 minutes, the reaction mixture was cooled to room temperature, diluted with CH2Cl2, filtered through powdered cellulose flock, stripped of solvent in vacuo, and was medium pressure chromatographed on silica gel using 13% EtOAc/hexane to give 306 mg of the title compound, 87% yield. Rf 0.29 in 15% EtOAc/hexane, visualized by UV and ammonium molybdate/ceric sulfate stain;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166206
Source datasetuspto-grants-1992_11
ORD IDord-fd0ccf9316f6413bb5fc53f3d5e5d4a3
Source noteuspto-grants-1992_11