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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794588Generated: November 4, 2026

Pyridine → HCID 11404180, compound

https://huagongshe.com/reaction/1794588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium IodideHCID 4875—
ReactantHCID 22222222HCID 22222222—
ReactantHCID 178418546HCID 178418546—
SolventEthyl AcetateHCID 8857—
ProductHCID 11404180HCID 11404180—

Reaction Conditions

Temperature100 °C

Reaction Steps

N-(5-Bromo-4-methyl-2-propylimidazol-1-yl)-2-ethoxybenzamide from Example 2a (0.5 g, 1.2 mmol) and copper(I) cyanide (0.3 g, 3.5 mmol) are introduced into 12.5 ml of pyridine and heated at 100° C. for 6 hours. Potassium iodide (23 mg, 0.56 mmol) is added to the mixture, which is then stirred for a further 6 hours at 100° C. The reaction mixture is cooled to room temperature and, after addition of 50 ml of ethyl acetate, washed with dilute alkaline H2O2 solution. The aqueous phase is re-extracted with ethyl acetate, and the combined ethyl acetate phase is concentrated, finally azeotroped with toluene and again concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022847B2
Source datasetuspto-grants-2006_04
ORD IDord-21204130c59a443198b5c1c02dd1113e
Source noteuspto-grants-2006_04