HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389728Generated: October 29, 2026
Ammonia → 5-(4-Methoxyphenyl)-2-phenyloxazole-4-carboxamide
https://huagongshe.com/reaction/389728
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Carbodiimide | HCID 160435 | — |
| Reactant | 5-(4-Methoxyphenyl)-2-phenyloxazole-4-carboxylic acid | HCID 20120402 | — |
| Reactant | 5-(4-Methoxyphenyl)-2-(thiophen-2-yl)oxazole-4-carboxylic acid | HCID 29281463 | — |
| Reactant | HCID 178526939 | HCID 178526939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(4-Methoxyphenyl)-2-phenyloxazole-4-carboxamide | HCID 59587431 | 27% |
Reaction Steps
To a solution of 5-(4-methoxyphenyl)-2-phenyloxazole-4-carboxylic acid (prepared according to the method described for 5-(4-methoxyphenyl)-2-(thiophen-2-yl)oxazole-4-carboxylic acid in Example M-1, 0.032 g, 0.11 mmol) and hydroxybenzotriazole monohydrate (0.02 g, 0.13 mmol) in DCM (2 mL) and DMF (1 mL) was added 0.5M ammonia in dioxane (1 mL, 0.5 mmol), followed by PS-carbodiimide resin. The resulting mixture was stirred at room temperature overnight. The mixture was passed through a MP-CO3 resin cartridge and the solvent removed in vacuo. The residue was purified by preparative HPLC to afford 5-(4-methoxyphenyl)-2-phenyloxazole-4-carboxamide (0.008 g, 0.03 mmol, 27%) as a white solid. 1H NMR (DMSO) δ 3.85 (3H, s), 7.10 (2H, d), 7.60 (3H, m), 7.66 (1H, br. s), 7.78 (1H, br. s), 8.14 (2H, m), 8.37 (2H, d). LCMS (2) Rt: 3.16 min; m/z (ES+) 295.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378095B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-8ab78547a8c34ef5901e28c81e11d08d |
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| Source note | uspto-grants-2013_02 |
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