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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397380Generated: November 1, 2026

3-[5-(Trifluoroacetyl)thiophen-2-yl]benzoic Acid → N-(2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropyl)-3-(5-(2,2,2-trifluoroacetyl)thiophen-2-yl)benzamide

https://huagongshe.com/reaction/1397380

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[5-(Trifluoroacetyl)thiophen-2-yl]benzoic AcidHCID 24896624—
Reactant2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amineHCID 67323086—
ProductN-(2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropyl)-3-(5-(2,2,2-trifluoroacetyl)thiophen-2-yl)benzamideHCID 673254785%

Reaction Steps

This compound was synthesized from 2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amine and 3-(5-(2,2,2-trifluoroacetyl)thiophen-2-yl)benzoic acid as described in example 8 step 6 (8 mg, yield 5%). 1H NMR (400 MHz, DMSO-d6) δ 8.53-8.50 (t, J=6.2 Hz, 1H), 8.21 (m, 1H), 8.17-8.16 (m, 1H), 8.03-7.98 (m, 4H), 7.93-7.91 (m, 1H), 7.88-7.87 (d, J=4.3 Hz, 1H), 7.63-7.59 (t, J=7.8 Hz, 1H), 7.34-7.30 (t, J=8.8 Hz, 2H), 3.52-3.50 (d, J=6.4 Hz, 2H), 1.29 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-960930f9e3564f99a19bec4b8626bb57
Source noteuspto-grants-2014_12