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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402269Generated: October 30, 2026

4-(Trifluoromethoxy)benzylamine → 3-(3,5-Dibromo-4-hydroxyphenyl)-N-(4-(trifluoromethoxy)benzyl)-1,2,4-oxadiazole-5-carboxamide

https://huagongshe.com/reaction/2402269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)benzylamineHCID 571846—
ReactantEthyl 3-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-5-carboxylateHCID 136139598—
SolventEthanolHCID 702—
Product3-(3,5-Dibromo-4-hydroxyphenyl)-N-(4-(trifluoromethoxy)benzyl)-1,2,4-oxadiazole-5-carboxamideHCID 13587047253.1%

Reaction Steps

A solution of the ethyl 3-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-5-carboxylate (78 mg, 0.2 mmol) plus 4-trifluoromethoxybenzyl amine (57 mg, 0.3 mmol) in ethanol (3 mL) was refluxed for 6 hours. The resulting solution was evaporated in vacuo and the residue was dissolved in ethyl acetate (2.5 mL) and washed with 1 N hydrochloric acid (2 mL), then water (2 mL). The organic layer was evaporated to dryness in vacuo and purified by preparative HPLC to give the title compound (57 mg, 53%) as a colourless powder. 1H NMR δ (ppm) (DMSO-d6): 4.55 (2 H, d), 7.38 (2 H, d), 7.51 (2 H, d), 10.07 (1 H, t), 10.95 (1 H, s, br). LCMS (10 cm_apci_formic) tR 4.14 min; m/z 534/536/538 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796321B2
Source datasetuspto-grants-2014_08
ORD IDord-55216fbb8c4849a78fe14d94191da941
Source noteuspto-grants-2014_08