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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 3-(3,5-Dibromo-4-(4-methoxybenzyloxy)phenyl)-N-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-5-carboxamide | HCID 57919734 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3,5-Dibromo-4-hydroxyphenyl)-n-ethyl-n-(3-(trifluormethyl)benzyl)-1,2,4-oxadiazole-5-carboxamide | HCID 135870535 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207205B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-c0c8247c40c7416f92070886877d5e7a |
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| Source note | uspto-grants-2012_06 |
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