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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222360Generated: October 31, 2026

Water → 3-(3,5-Dibromo-4-hydroxyphenyl)-n-ethyl-n-(3-(trifluormethyl)benzyl)-1,2,4-oxadiazole-5-carboxamide

https://huagongshe.com/reaction/222360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantSodium t-butoxideHCID 23676156—
Reactant3-(3,5-Dibromo-4-(4-methoxybenzyloxy)phenyl)-N-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-5-carboxamideHCID 57919734—
SolventDimethylformamideHCID 6228—
Product3-(3,5-Dibromo-4-hydroxyphenyl)-n-ethyl-n-(3-(trifluormethyl)benzyl)-1,2,4-oxadiazole-5-carboxamideHCID 13587053532%

Reaction Steps

3-(3,5-Dibromo-4-(4-methoxybenzyloxy)phenyl)-N-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-5-carboxamide (128 mg, 0.2 mmol) was dissolved in dimethylformamide (2 mL) and sodium-tert-butoxide (21 mg, 0.22 mmol) was added in one portion followed by ethyl iodide (34 mg, 0.22 mmol). The mixture was stirred at room temperature for 20 h and was then treated with water (8 mL) and extracted with ethyl acetate (4 mL). The extract was evaporated to dryness and the residue was dissolved in dichloromethane (2 mL), trifluoroacetic acid (0.2 mL) was added and the solution was allowed to stand for 1 h. Methanol (0.5 mL) was added, the solution was evaporated to dryness and the residue was purified by preparative HPLC to give the title compound (32.8 mg, 32%) as a colourless solid. 1H NMR δ (ppm) (DMSO-d6): 1.14 and 1.29 (3H, two t), 3.47 and 3.62 (2H, two q), 4.88 and 4.97 (2H, two s), 7.60-7.75 (3H, m), 7.78 and 7.89 (1H, two s), 8.04 and 8.15 (2H, two s), 10.9 (1H, s, br). LCMS (10 cm_apci_formic) tR 4.33 min; m/z 546/548/550 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207205B2
Source datasetuspto-grants-2012_06
ORD IDord-c0c8247c40c7416f92070886877d5e7a
Source noteuspto-grants-2012_06