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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874998Generated: October 31, 2026

3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid → (3-(5-(4-Fluorophenyl)oxazol-2-yl)piperidin-1-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl)methanone

https://huagongshe.com/reaction/874998

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 25180854—
Reactant5-(4-Fluorophenyl)-2-(piperidin-3-yl)oxazole TFA SaltHCID 86673536—
Product(3-(5-(4-Fluorophenyl)oxazol-2-yl)piperidin-1-yl)(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl)methanoneHCID 533278869%

Reaction Steps

This compound was synthesized from 5-(4-fluorophenyl)-2-(piperidin-3-yl)oxazole TFA salt and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described for example 37 step 3 (25 mg, yield 9%). 1H NMR (400 MHz, DMSO-d6, 80° C.) δ 8.11-8.09 (m, 1H), 7.97 (s, 1H), 7.69-7.61 (m, 4H), 7.45 (s, 1H), 7.24-7.20 (t, J=8.8 Hz, 2H), 4.16 (m, 1H), 3.71-3.67 (m, 1H), 3.62-3.56 (dd, J=12.9 Hz, 8.4 Hz, 1H), 3.47-3.41 (m, 1H), 3.24-3.18 (m, 1H), 2.22-2.17 (m, 1H), 2.03-1.94 (m, 1H), 1.89-1.84 (m, 1H), 1.69-1.59 (m, 1H). MS (ESI) m/z: Calculated for C24H18F4N4O3: 486.13. found: 487.3 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981084B2
Source datasetuspto-grants-2015_03
ORD IDord-0a6b8e10e9314a6fba92e2cd97e1c617
Source noteuspto-grants-2015_03