Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491784Generated: October 30, 2026

Imidazole → HCID 178497419, compound

https://huagongshe.com/reaction/491784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178484810HCID 178484810—
SolventFormic AcidHCID 284—
SolventChloroformHCID 6212—
ProductHCID 178497419HCID 178497419—

Reaction Steps

To a solution of imidazole (783 mg) and triethylamine (2.41 ml) in chloroform (80 ml) is added dropwise formic acid (709 μl) with stirring under ice-cooling. Oxalyl chloride (1.00 ml) in chloroform (10 ml) is further added thereto, and the mixture is stirred at room temperature for 0.5 hour. The reaction solution is cooled again with ice, and thereto is added trans-5-methoxycarbonyl-3-[4-(methylamino)cyclohexylcarbonylamino]-N-(5-chloropyridine-2-yl)benzofuran-2-carboxamide hydrochloride (1.50 g) obtained in Example 218. The mixture is warmed to room temperature and stirred for 3 hours. To the reaction solution are poured ice-water and a saturated aqueous sodium hydrogen carbonate solution, and the mixture is extracted with chloroform. The extract is washed with a saturated brine, and dried over sodium sulfate. The solvent is evaporated under reduced pressure, and the resulting residue is purified by NH-silica gel column chromatography (eluent: chloroform) to give the title compound (1.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531537B2
Source datasetuspto-grants-2009_05
ORD IDord-19160bea9d94499c92397cfe57527252
Source noteuspto-grants-2009_05