HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744552Generated: October 30, 2026
5-Amino-2-(piperidin-1-yl)benzonitrile → N-(3-Cyano-4-piperidinophenyl)-1,5-dimethylpyrazole-4-carboxamide
https://huagongshe.com/reaction/1744552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Amino-2-(piperidin-1-yl)benzonitrile | HCID 10845751 | — |
| Reactant | 1-Hydroxybenzotriazole 1,5-dimethylpyrazole-4-carboxylate | HCID 22228208 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-Cyano-4-piperidinophenyl)-1,5-dimethylpyrazole-4-carboxamide | HCID 22228107 | 49.7% |
Reaction Steps
1-Hydroxybenzotriazole 1,5-dimethylpyrazole-4-carboxylate (1.2 g) and 5-amino-2-piperidinobenzonitrile (0.9 g) were added to ethanol (20 ml) and the mixture was stirred at 78° C. for 3 h. After evaporation of the solvent, aqueous potassium carbonate solution was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. n-Hexane was added to the residue to allow crystallization. The crystals were recrystallized from hydrous ethanol to give the title compound (0.7 g), melting point: 217–218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07015218B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-21eeb7599b8c4d37a0462f8b5b9a2398 |
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| Source note | uspto-grants-2006_03 |
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