HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577135Generated: October 28, 2026
Water → N,N-dimethyl-1H-pyrazole-1-sulfonamide
https://huagongshe.com/reaction/577135
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-dimethyl-1H-pyrazole-1-sulfonamide | HCID 10954038 | — |
Reaction Steps
To a solution of sodium hydride (5.2 g, 130 mmol, 60% in mineral oil) in anhydrous THF (50 mL) was added a solution of 1H-pyrazole (5.92 g, 87 mmol) in anhydrous THF (100 mL) at 0° C. The mixture was stirred for 30 minutes at room temperature. Dimethylsulfamoyl chloride (13.9 mL, 130 mmol) was added at 0° C., and then the mixture was stirred for 1.5 hours at room temperature. Water was added, and the mixture was extracted 3 times with ethyl acetate. The organic phase was washed with brine and dried over sodium sulfate. After evaporation of the solvent, the oil was passed through a short silica gel column using 20% hexane/ethyl acetate as a solvent. N,N-dimethyl-1H-pyrazole-1-sulfonamide was obtained as a yellow oil and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040538B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-151fe3815de64e2aa68ac341b8b92eff |
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| Source note | uspto-grants-2015_05 |
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