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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181057Generated: November 4, 2026

Pyridine → HCID 22485126, compound

https://huagongshe.com/reaction/2181057

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 numberUS06890934B2
Source datasetuspto-grants-2005_05
ORD IDord-fa44bd8425a64863b19f7df100a08540
Source noteuspto-grants-2005_05