Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466714Generated: October 31, 2026

HCID 178418546, compound → HCID 178437440, compound

https://huagongshe.com/reaction/466714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178437403HCID 178437403—
SolventPyridineHCID 1049—
ProductHCID 178437440HCID 17843744071.5%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 5-bromo-2-ethyl-7-methyl-3-(2'-(tetrazol-5-yl)biphen-4-yl)methyl-3H-imidazo[4,5-b]pyridine (41 mg), CuCN (80 mg), and pyridine (0.2 mL) was heated with stirring to 160° C. for 4 hours. The pyridine distilled off during the course of the heating. The cooled dark mass was dissolved in 2 mL of 20% aqueous KCN by heating to 50° C. for 15 minutes. Acetic acid (2 mL) (Caution! HCN is evolved.) was added and the mixture was extracted (2×EtOAc). The organic layers were dried (Na2SO4), concentrated, and purified (SiO2, 80/20/1 CH2Cl2 --MeOH--NH4OH) to give 26 mg of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157026
Source datasetuspto-grants-1992_10
ORD IDord-d659d70890534325bdadf4ec9eb1f9ee
Source noteuspto-grants-1992_10