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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52147Generated: October 28, 2026

Potassium Carbonate → 2-Chloromethyl-3-methyl-4-(2-morpholinoethylthio)pyridine

https://huagongshe.com/reaction/52147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridineHCID 19963039—
SolventChloroformHCID 6212—
Product2-Chloromethyl-3-methyl-4-(2-morpholinoethylthio)pyridineHCID 19963034—

Reaction Steps

2-Hydroxymethyl-3-methyl-4-(2-morpholinoethylthio)pyridine (6.2 g) was dissolved in chloroform and thereto was dropwise added thionyl chloride (2 ml) under ice-cooling. The mixture was stirred at room temperature for 1 hour. After the completion of the reaction, the reaction mixture was poured into ice-water and made alkaline with potassium carbonate, followed by extraction with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and the solvent was distilled away to give 6.0 g of 2-chloromethyl-3-methyl-4-(2-morpholinoethylthio)pyridine as an oily substance. The substance was added to ethanol (60 ml) containing a solution of 5-methoxycarbonyl-2-mercaptobenzimidazole (5.1 g) and sodium hydroxide (1.6 g) in water (10 ml) and the mixture was refluxed under heating for 3.5 hours. After the completion of the reaction, the ethanol was distilled away and the residue was dissolved in water. The aqueous layer was washed with chloroform and dilute hydrochloric acid was dropwise added until crystals precipitated in the aqueous layer. The resultant crystals were collected by filtration to give 2-((3-methyl-4-(2-morpholinoethylthio)-2-pyridyl)methylthio)-1H-benzimidazole-5-carboxylic acid 7/2 hydrate, melting point 120-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616581
Source datasetuspto-grants-1997_04
ORD IDord-08ea5931942443ea820a27a8f8b71b72
Source noteuspto-grants-1997_04