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2-Bromoacetamidopyridine → 2-(3-Chlorophenyl)-4-(pyridin-2-yl)-1,3-oxazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromoacetamidopyridine | HCID 38384 | — |
| 反応物 | 3-Chlorobenzamide | HCID 69254 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-(3-Chlorophenyl)-4-(pyridin-2-yl)-1,3-oxazole | HCID 10220745 | 24.7% |
反応手順
Using the procedures of Kelly et al., J. Org. Chem., (1996) 61:4623-4633, a solution of 2-bromoacetylpyridine (120 mg, 0.6 mmol) in toluene (5 mL) was treated with 3-chlorobenzamide (300 mg, 1.9 mmol) and the mixture heated in a sealed vial at reflux for 60 hours. The mixture was then cooled and the solvent was removed in vacuo. Silica gel chromatography using a gradient of hexane to ethyl acetate afforded 38 mg (9%) of 2-[3-chlorophenyl]-4-[pyridin-2-yl]-1,3-oxazole as a pale yellow solid. 1H-NMR (CDCl3), δ (ppm): 8.62 (d, 1H), 8.35 (s, 1H), 8.15 (m, 1H), 8.00 (m, 2H), 7.80 (td, 1H), 7.42 (m, 2H), 7.23 (m, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06660753B2 |
| 出典データセット | uspto-grants-2003_12 |
| ORD ID | ord-5a4391cd3386466e96efcf6ba2193b0c |
| 出典メモ | uspto-grants-2003_12 |