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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 66707286HCID 66707286—
SolventDimethylformamideHCID 6228—
ProductHCID 58071748HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791272B2
Source datasetuspto-grants-2014_07
ORD IDord-595de646f3cc4ef5a1c6a8044b97e662
Source noteuspto-grants-2014_07