Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794586Generated: November 2, 2026

Pyridine → HCID 11404180, compound

https://huagongshe.com/reaction/1794586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 11269925HCID 11269925—
ReactantHCID 178418546HCID 178418546—
SolventDichloromethaneHCID 6344—
ProductHCID 11404180HCID 11404180—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Ethoxy-N-(5-iodo-4-methyl-2-propylimidazol-1-yl)benzamide from Example 1a (0.5 g, 1.2 mmol) and copper(I) cyanide (0.7 g, 7.5 mmol) are introduced into 10 ml of pyridine and heated at 100° C. for three hours. The reaction mixture is cooled to room temperature, 50 ml of dichloromethane are added, and the solid is removed by filtration. The filtrate is washed three times with 50 ml of water each time, and the organic phase is re-extracted with 50 ml of dichloromethane. The combined organic phase is dried with sodium sulphate and concentrated. To remove the remaining pyridine, the residue is taken up in 50 ml of dichloromethane and washed six times with 100 ml of water each time. The organic phase is dried with sodium sulphate and concentrated in a rotary evaporator. The residue is finally mixed with 100 ml of toluene and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022847B2
Source datasetuspto-grants-2006_04
ORD IDord-2a36c94fa61e4ed1ac847e6bc3e4f08b
Source noteuspto-grants-2006_04