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HRID 731608作成日:2026年10月26日

2-Aminopyridine → HCID 24738180、化合物

https://huagongshe.com/reaction/731608

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminopyridineHCID 10439—
反応物Sodium BicarbonateHCID 516892—
反応物4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
溶媒EthanolHCID 702—
生成物HCID 24738180HCID 2473818055%

反応手順

A mixture of 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) and 2-aminopyridine (47 mg, 0.5 mmol) in ethanol (3.1 mL) was heated under reflux under argon for 3.5 h. Then another portion of 2-aminopyridine (24 mg, 0.25 mmol) was added and heating under reflux continued for another 1 h. The resulting mixture was then cooled to room temperature and then sodium hydrogen carbonate (63 mg, 0.75 mmol) added and the resulting mixture heated under reflux for 2 h. After cooling to room temperature, the mixture was poured onto water and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over sodium sulphate and evaporated to leave a yellow oil. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50) afforded the title compound (76 mg, 55%) which was obtained as a light yellow gum. MS: m/e=276.0 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585874B2
出典データセットuspto-grants-2009_09
ORD IDord-696ff80f9aef4bb98014deb962024899
出典メモuspto-grants-2009_09