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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601673Generated: October 29, 2026

Sodium Acetate → 4-(thiazolo[5,4-b]pyridine-2-yl)-1-(2-chlorophenyl)-5-methyl-1H-[1,2,3]triazole

https://huagongshe.com/reaction/601673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantThiazolo(5,4-b)pyridineHCID 19831912—
Reactant1-(2-Chlorophenyl)-4-iodo-5-methyl-[1,2,3]-triazoleHCID 23158267—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(thiazolo[5,4-b]pyridine-2-yl)-1-(2-chlorophenyl)-5-methyl-1H-[1,2,3]triazoleHCID 231581608.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

Under nitrogen atmosphere, 344 mg of 1-(2-chlorophenyl)-4-iodo-5-methyl-[1,2,3]-triazole and 276 mg of thiazolo(5,4-b)pyridine (B. Stanovnik, Synthesis, 1974, 120) were dissolved in 3 ml of DMF. Then, 100 mg of sodium acetate and 103 mg of Herrman catalyst were added, and the mixture was stirred at 140° C. for 8 hours. After diluting the reaction solution with water, the resultant was extracted with chloroform. Organic layer was washed with saturated saline solution, and dried with anhydrous sodium sulfate. The residues obtained by distilling out the solvents were separated and purified by thin-layer silicagel column chromatography (ethyl acete/hexane=1/1) to obtain 30 mg of the above compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-5b3301b88e2c4c008ac9c0ca8bedb795
Source noteuspto-grants-2011_03