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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381898Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 14369790, compound

https://huagongshe.com/reaction/1381898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-Methyl-5-(4-pyridinyl)thiazole-2-carboxamideHCID 129441—
SolventPyridineHCID 1049—
ProductHCID 14369790HCID 1436979053.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

p-Toluenesulfonyl chloride (860 mg) was added to a stirred suspension of 4-methyl-5-(4-pyridinyl)-thiazole-2-carboxamide (450 mg) in dry pyridine (5 ml) under ice-cooling, and the mixture was stirred at 90° C. for 21 hours. The mixture was evaporated to dryness, and the residue was dissolved 2N hydrochloric acid aqueous solution (10-15 ml), washed twice with chloroform, and made alkaline by addition of 2N sodium hydroxide aqueous solution. The resulting precipitates were extracted with chloroform, washed with water, dried over magnesium sulfate, and evaporated to dryness. The residue was washed with petroleum ether, and was recrystallized from iso-propanol (twice) to give 2-cyano-4-methyl-5-(4-pyridinyl)-thiazole (220 mg, yield 53%) as pale yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804668
Source datasetuspto-grants-1989_02
ORD IDord-8bad51cfa40d48488cf96cb4c96f4baa
Source noteuspto-grants-1989_02