Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373508Generated: October 30, 2026

Pyridine → HCID 16221117, compound

https://huagongshe.com/reaction/2373508

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 numberUS07459452B2
Source datasetuspto-grants-2008_12
ORD IDord-acf213ac929e412da764443acccc3fd5
Source noteuspto-grants-2008_12