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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397385Generated: October 30, 2026

2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amine → 2-Fluoro-N-(2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropyl)-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

https://huagongshe.com/reaction/1397385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amineHCID 67323086—
Reactant2-Fluoro-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 67323899—
Product2-Fluoro-N-(2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropyl)-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamideHCID 6995037332%

Reaction Steps

This compound was synthesized from 2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amine and 2-fluoro-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described in example 8 step 6 (75 mg, yield 32%) as a yellow viscous liquid. 1H NMR (400 MHz, MeOD) δ 8.46-8.43 (dd, J=6.8 Hz, 2.3 Hz, 1H), 8.29-8.25 (ddd, J=8.7 Hz, 4.8 Hz, 2.4 Hz, 1H), 8.09-8.05 (dd, J=9.0 Hz, 5.3 Hz, 2H), 7.77 (s, 1H), 7.47-7.42 (dd, J=10.3 Hz, 8.8 Hz, 1H), 7.25-7.20 (t, J=8.9 Hz, 2H), 3.67 (s, 2H), 1.41 (s, 6H). MS (ESI) m/z: Calculated for C23H17F6N4O3: 492.12. found: 493.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-a616e4058cd641669c81194338747ac1
Source noteuspto-grants-2014_12