Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874948Generated: October 30, 2026

3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid → 6-(1-(3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoyl)azetidin-3-yl)nicotinonitrile

https://huagongshe.com/reaction/874948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 25180854—
Reactant6-(azetidin-3-yl)nicotinonitrile TFA saltHCID 86673532—
Product6-(1-(3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoyl)azetidin-3-yl)nicotinonitrileHCID 5332781147%

Reaction Steps

This compound was synthesized from 6-(azetidin-3-yl)nicotinonitrile TFA salt and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described for example 37 step 3 (70 mg, yield 47%). 1H NMR (400 MHz, DMSO-d6) δ 9.06 (m, 1H), 8.30-8.29 (m, 2H), 8.21-8.19 (d, J=7.8 Hz, 1H), 7.96-7.94 (d, J=7.8 Hz, 1H), 7.74-7.70 (t, J=7.7 Hz, 1H), 7.63-7.61 (d, J=8.1 Hz, 1H), 4.76-4.72 (m, 1H), 4.52-4.46 (m, 2H), 4.25-4.18 (m, 2H). MS (ESI) m/z: Calculated for C19H12F3N5O2: 399.09. found: 400.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981084B2
Source datasetuspto-grants-2015_03
ORD IDord-907124eb5b87454aa472bac6fc187946
Source noteuspto-grants-2015_03