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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368265Generated: October 31, 2026

Pyridine → HCID 22485126, compound

https://huagongshe.com/reaction/1368265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 22485111HCID 22485111—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 22485126HCID 2248512689.6%

Reaction Steps

To a suspension of 3-(2-chloro-4-(methylamino)benzyl)-2-methyl-5-(1-pentanesulfonylcarbamoyl)-3H-imidazo[4,5-b]pyridine (188 mg) in dichloromethane (1.9 ml) were added pyridine (58 mg) and pivaloyl chloride (65 mg) at room temperature and the mixture was stirred for 2 days. The reaction mixture was diluted with chloroform, washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated and ethanol was added to the residue to give crude crystals. Ethanol was evaporated, and the residue was recrystallized from acetone-water to give 3-(2-chloro-4-(methyl(pivaloyl)amino)benzyl)-2-methyl-5-(1-pentanesulfonylcarbamoyl)-3H-imidazo[4,5-b]pyridine (199 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573274B1
Source datasetuspto-grants-2003_06
ORD IDord-3cd596fa33204f56b1cd2c31bde2fab1
Source noteuspto-grants-2003_06