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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856802Generated: November 1, 2026

Potassium Carbonate → HCID 178526848, compound

https://huagongshe.com/reaction/1856802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-nitrothiazoleHCID 18211—
ReactantHCID 178518948HCID 178518948—
SolventEthanolHCID 702—
ProductHCID 178526848HCID 17852684818.7%

Reaction Steps

The title compound was prepared by the general method described by Potts, K. T. (1961) Chem. Rev. 61:87. 4-Phenyl-3-thiosemicarbazide (4.18 g) (Aldrich) was dissolved in 50 mL of pyridine and treated with 2.71 g of ethyl chloroformate at 0° C. The reaction was stirred for 2 hours and then refluxed for 18 hours. Evaporation of the solvent and trituration with water gave 2.5 g of 3-hydroxy-5-mercapto-4-phenyl-1,2,4-triazole. 3-Hydroxy-5-mercapto-4-phenyl-1,2,4-triazole (1.93 g) was stirred in 10 mL of ethanol with 1.1 equivalent of potassium carbonate in 10 mL ethanol for one hour and then reacted with 2.09 g of 2-bromo-5-nitrothiazole as in Example 1. Crystallization from ethanol and water gave 0.6 g of 3-hydroxy-5-[(5-nitrothiazol-2-yl)mercapto]-4-phenyl-1,2,4-triazole, a dark yellow solid, M.P. 188-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143765
Source datasetuspto-grants-2000_11
ORD IDord-6dfe6d8a670442f8af634927745a3e0e
Source noteuspto-grants-2000_11