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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767111Generated: November 1, 2026

Pyridine → HCID 16221117, compound

https://huagongshe.com/reaction/1767111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
Reactantp-TolunitrileHCID 7724—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178476733HCID 178476733—
SolventDichloromethaneHCID 6344—
ProductHCID 16221117HCID 16221117—

Reaction Steps

A mixture of dihydroxypyrimidine methylcarboxylate (B-1) (prepared from 4-methylbenzonitrile by procedures similar to those set forth in Scheme A), 4 eq. of benzoylchloride and 8 eq. of dry pyridine was stirred in dry dichloromethane at room temperature over night. The reaction mixture was diluted with EtOAc and the organic layer was washed twice with 1N HCl, once with brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The solid residue was triturated with diethyl ether to give product (B-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232819B2
Source datasetuspto-grants-2007_06
ORD IDord-69e163cc37bb444a8632a79d43d6dd98
Source noteuspto-grants-2007_06