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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570326Generated: October 31, 2026

Cyanogen Bromide → N-(5-cyanamido-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/570326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium AcetateHCID 517044—
ReactantN-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677450—
SolventMethanolHCID 887—
ProductN-(5-cyanamido-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86677452—

Reaction Steps

To N-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (67) (4.53 g, 15 mmol) in MeOH (100 mL) was added KOAc (4.41 g, 45 mmol) and the mixture was stirred at room temperature for 5 minutes then cooled to 0° C. before a solution of BrCN (1.62 g, 15 mmol) in MeOH (30 mL) was added dropwise. The resulting mixture was slowly warmed to room temperature and stirred overnight. The solvent was evaporated and to the residue was added water (150 mL). The mixture was stirred at room temperature for 1 hour, filtered and washed with water (2×20 mL), then air dried to give N-(5-cyanamido-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (68) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023839B2
Source datasetuspto-grants-2015_05
ORD IDord-4ed9e57a0e9947d1854e2a4f94ee4b30
Source noteuspto-grants-2015_05