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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397403Generated: October 30, 2026

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

https://huagongshe.com/reaction/1397403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amineHCID 67323086—
Reactant2-Methoxy-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 67325651—
ProductN-(2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropyl)-2-methoxy-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamideHCID 7124492036%

Reaction Steps

This compound was synthesized from 2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amine and 2-methoxy-5-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described in example 8 step 6 (40 mg, yield 36%). 1H NMR (400 MHz, MeOD) δ 8.64-8.63 (d, J=2.3 Hz, 1H), 8.45-8.42 (t, J=5.6 Hz, 1H), 8.24-8.21 (dd, J=8.8 Hz, 2.4 Hz, 1H), 8.11-8.07 (m, 2H), 7.83 (s, 1H), 7.34-7.32 (d, J=8.8 Hz, 1H), 7.27-7.23 (t, J=8.8 Hz, 2H), 3.91 (s, 3H), 3.72-3.71 (m, 2H), 1.41 (s, 6H). MS (ESI) m/z: Calculated for C24H20F4N4O4: 504.14. found: 505.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-ffa37534c5c84424b0f276f95ee0ab69
Source noteuspto-grants-2014_12