HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052217Generated: October 31, 2026
Pyrazole → N,N-dimethyl-1H-pyrazole-1-sulfonamide
https://huagongshe.com/reaction/1052217
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-dimethyl-1H-pyrazole-1-sulfonamide | HCID 10954038 | — |
Reaction Steps
Pyrazole (12 g) was dissolved in tetrahydrofuran (200 mL), sodium hydride (60% in oil, 8.46 g) was added at 0° C. with stirring under a nitrogen atmosphere. After 20 min, dimethylsulfamoyl chloride (17 mL) was added dropwise, and the mixture was further stirred at the same temperature for 1 hr, and at room temperature for 1 hr. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate (400 mL), the mixture was extracted with ethyl acetate (400 mL), and the extract was dried over anhydrous magnesium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane), and the object fraction was concentrated under reduced pressure to give the title compound (25.3 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388195B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-7f18d2dfd5164d9b9ca5a9954dba779a |
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| Source note | uspto-grants-2016_07 |
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