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HRID 431898作成日:2026年10月26日

2-Bromoacetamidopyridine → 2-(3-Chlorophenyl)-4-(pyridin-2-yl)-1,3-oxazole

https://huagongshe.com/reaction/431898

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromoacetamidopyridineHCID 38384—
反応物3-ChlorobenzamideHCID 69254—
溶媒TolueneHCID 1140—
生成物2-(3-Chlorophenyl)-4-(pyridin-2-yl)-1,3-oxazoleHCID 1022074524.7%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660753B2
出典データセットuspto-grants-2003_12
ORD IDord-5a4391cd3386466e96efcf6ba2193b0c
出典メモuspto-grants-2003_12