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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538108Generated: October 30, 2026

Potassium Carbonate → HCID 66937318, compound

https://huagongshe.com/reaction/538108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylsulphamoyl chlorideHCID 83372—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
Reactant2,5,6-Trichloro-1H-benzimidazoleHCID 286009—
ReactantHCID 66937410HCID 66937410—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66937318HCID 66937318—

Reaction Steps

2,5,6-Trichloro-1H-benzoimidazole 2 (27.6 g, 0.125 mol) was dissolved in dry DMF (200 mL) and then K2CO3 (20.7 g, 0.15 mol) and dimethylsulfamoyl chloride (17.9 g, 0.125 mol) were added. The reaction mixture was stirred at room temperature for 16 hours. HPLC analysis showed the complete formation of 2,5,6-trichloro-benzoimidazole-1-sulfonic acid dimethylamide. In the same pot, without isolation of 2,5,6-trichloro-benzoimidazole-1-sulfonic acid dimethylamide, was added 1H-pyrazole-4-carboxylic acid ethyl ester (17.5 g, 0.125 mol) and K2CO3 (20.7 g, 0.15 mol). The reaction mixture was stirred at 70° C. for 4 hours and water (500 mL) was added while the reaction solution was still hot. The reaction solution was cooled to room temperature. The precipitated solid was collected via filtration, washed with water and dried. The crude product was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865713B2
Source datasetuspto-grants-2014_10
ORD IDord-0008468401c74b15a2d0aae65e5a5b44
Source noteuspto-grants-2014_10