Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86757789 | HCID 86757789 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22288394 | HCID 22288394 | 60.5% |
Reaction Steps
A mixture of ethyl 1-(4-(4-chlorobenzoylamino)phenyl-5-trifluoromethyl-1H-pyrazole-4-carboxylate (150 mg), 1 N sodium hydroxide aqueous solution (1 ml) and ethanol (2 ml) was stirred at 45° C. for 4 hours. after spontaneous cool, 1 N hydrochloric acid aqueous solution (2 ml) was added to the reaction solution, the thus formed product was extracted with ethyl acetate and then the extract was washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under a reduced pressure. The resulting residue was recrystallized from ethanol to give 1-[4-(4-chlorobenzoylamino)phenyl]-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (91 mg) as colorless powder crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06348480B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-1205430eebe3484081ddebb9ede419e8 |
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| Source note | uspto-grants-2002_02 |
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