HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538108Generated: October 30, 2026
Potassium Carbonate → HCID 66937318, compound
https://huagongshe.com/reaction/538108
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | ethyl 1H-pyrazole-4-carboxylate | HCID 142179 | — |
| Reactant | 2,5,6-Trichloro-1H-benzimidazole | HCID 286009 | — |
| Reactant | HCID 66937410 | HCID 66937410 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66937318 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865713B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-0008468401c74b15a2d0aae65e5a5b44 |
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| Source note | uspto-grants-2014_10 |
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