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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114135Generated: October 31, 2026

4'-Trifluoromethyl-biphenyl-3-carboxylic acid → HCID 69202928, compound

https://huagongshe.com/reaction/2114135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-Trifluoromethyl-biphenyl-3-carboxylic acidHCID 2782718—
Reactant5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamideHCID 11300488—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69202928HCID 6920292867.1%

Reaction Steps

5′-Amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl-4-carboxamide (53 mg, 0.189 mmol) and 3-(4-trifluoromethylphenyl)benzoic acid (151 mg, 0.57 mmol) were mixed in THF (5 ml) and the mixture shaken in a varian tube for 15 min at room temperature. Carbodiimde resin (500 mg) was added and shaking continued for 18 h. The solution was filtered off and concentrated under vacuum. The residue was chromatographed on a silica gel flash column eluting with ethyl acetate/hexane (1:1) and the solvent evaporated under vacuum to give N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-3-(4-trifluoromethylphenyl)benzamide (67 mg, 67%). NMR; δH CDCl3 8.11,(1H, t), 7.87-7.85,(2H, m), 7.83,(2H, d), 7.77,(1H, m), 7.72,(4H, s), 7.63-7.57,(2H, m), 7.50,(1H, d), 7.41,(2H, d), 7.30,(1H, d), 6.25,(1H, t), 3.34,(2H, m), 2.24,(3H, s), 1.08,(1H, m), 0.57,(2H, m), 0.29,(2H, m). LCMS: retention time 4.01 min, MH+529.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432289B2
Source datasetuspto-grants-2008_10
ORD IDord-b5cb26c4924d4cdb96434759f2065f52
Source noteuspto-grants-2008_10