HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631905Generated: October 29, 2026
4-(Trifluoromethyl)benzoic acid → HCID 58071748, compound
https://huagongshe.com/reaction/1631905
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethyl)benzoic acid | HCID 9966 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 66707286 | HCID 66707286 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58071748 | HCID 58071748 | — |
Reaction Steps
Coupling: To a solution of [1-(4-amino-benzyl)-3,5-diethyl-1H-pyrazol-4-yl]-acetic acid tert-butyl ester (intermediate 2.1.2, 99 mg, 0.29 mmol) in dimethylformamide (1.5 mL) was added 4-(trifluoromethyl)benzoic acid (67 mg, 0.34 mmol), diisopropylethylamine (90 μL, 0.53 mmol) and TBTU (82 mg, 0.25 mmol). The reaction mixture was stirred for 18 h at room temperature. The reaction mixture was treated with aqueous K2CO3 solution (2 M, 0.15 mL) and filtered over Alox B, eluting with 10% methanol in dichloromethane. Cleavage of tert-butyl ester: The volatiles were removed under reduced pressure and the residue was treated with trifluoroacetic acid (2 mL). After 42 h, the mixture was concentrated under reduced pressure and purified via preparative reversed phase HPLC (gradient of methanol in water+0.1% NH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791272B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-595de646f3cc4ef5a1c6a8044b97e662 |
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| Source note | uspto-grants-2014_07 |
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