HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750449Generated: October 31, 2026
Water → 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carbonitrile
https://huagongshe.com/reaction/1750449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | 1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamide | HCID 86721179 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carbonitrile | HCID 86721289 | 92.7% |
Reaction Steps
To a solution of 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamide (500 mg, 1.91 mmol) in DMF (4 mL) was added cyanuric chloride (0.267 mL, 1.91 mmol) at 0° C., and the mixture was stirred at 0° C. for 14 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5→50% ethyl acetate/hexane) to give 1-(tert-butyl)-5-(4-fluorophenyl)-1H-pyrazole-4-carbonitrile (430 mg, 1.77 mmol, 92%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156837B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-a80c1ecc3f6040d0bb52459d99c939a2 |
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| Source note | uspto-grants-2015_10 |
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