HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631903Generated: October 29, 2026
4-(Trifluoromethyl)benzoic acid → {3,5-Dimethyl-1-[4-(4-trifluoromethyl-benzoylamino)-benzyl]-1H-pyrazol-4-yl}-acetic acid
https://huagongshe.com/reaction/1631903
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 | [1-(4-aminobenzyl)-3,5-dimethyl-1H-pyrazol-4-yl]acetic acid methyl ester | HCID 66707335 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {3,5-Dimethyl-1-[4-(4-trifluoromethyl-benzoylamino)-benzyl]-1H-pyrazol-4-yl}-acetic acid | HCID 58071835 | — |
Reaction Steps
Coupling: To a solution of [1-(4-amino-benzyl)-3,5-dimethyl-1H-pyrazol-4-yl]-acetic acid methyl ester (intermediate 1.1.3, 85 mg, 0.26 mmol) in dimethylformamide (1 mL) was added 4-(trifluoromethyl)benzoic acid (62 mg, 0.32 mmol), diisopropylethylamin (90 μL, 0.53 mmol) and TBTU (94 mg, 0.29 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. Saponification: The volatiles were removed under reduced pressure and the remaining residue was treated with aqueous NaOH solution (4 M, 0.2 mL). The mixture was 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-4ea5eab7c51740ac81585ea35e82f8b0 |
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| Source note | uspto-grants-2014_07 |
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