戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 83297作成日:2026年10月26日

Diisopropylethylamine → 6-{[3-(3-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinic acid methyl ester

https://huagongshe.com/reaction/83297

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Methyl 6-chloropyridine-3-carboxylateHCID 254249—
反応物C-[3-(3-Fluoro-phenyl)-5-methyl-isoxazol-4-yl]-methylamineHCID 67157896—
溶媒Dimethyl SulfoxideHCID 679—
生成物6-{[3-(3-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinic acid methyl esterHCID 6844478238%

反応条件

温度160 °C

反応手順

A mixture of C-[3-(3-fluoro-phenyl)-5-methyl-isoxazol-4-yl]-methylamine (530 mg, 2.6 mmol), methyl 6-chloronicotinate (440 mg, 2.6 mmol), N,N-diisopropyl ethyl amine (880 μL, 5.1 mmol) and DMSO (5.1 mL) was heated in the microwave to 160° C. for 2×0.5 h and 1 h. The mixture was then diluted with ice-water and extracted with ethyl acetate. The combined organic extracts were then washed with brine and dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 1:1) afforded the title compound (335 mg, 38%) as a yellow gum. MS: m/e=342.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846719B2
出典データセットuspto-grants-2014_09
ORD IDord-38e87361133b4831a4806240277a90f2
出典メモuspto-grants-2014_09