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HRID 854687作成日:2026年10月26日

Potassium Iodide → 2-[(e)-2-(2-Fluoro-4-trifluoromethyl-phenyl)-vinyl]-4-[4-(4-imidazol-1-ylmethyl-thiazol-2-yl)-phenoxymethyl]-oxazole

https://huagongshe.com/reaction/854687

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Cesium carbonateHCID 10796—
反応物4-Chloromethyl-2-[2-(2-fluoro-4-trifluoromethyl-phenyl)-vinyl]-oxazoleHCID 69072365—
反応物4-[4-(Imidazol-1-ylmethyl)-thiazol-2-yl]-phenolHCID 136355233—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物2-[(e)-2-(2-Fluoro-4-trifluoromethyl-phenyl)-vinyl]-4-[4-(4-imidazol-1-ylmethyl-thiazol-2-yl)-phenoxymethyl]-oxazoleHCID 6942638133.4%

反応条件

温度60 °C

反応手順

A mixture of 0.129 g (0.50 mmol) 4-[4-(imidazol-1-ylmethyl)-thiazol-2-yl]-phenol and 0.10 g (0.30 mmol) cesium carbonate in 10 ml butanone was stirred at 60° C. for 30 min, then 0.153 g (0.50 mmol) 4-chloromethyl-2-[2-(2-fluoro-4-trifluoromethyl-phenyl)-vinyl]-oxazole and 0.083 g (0.50 mmol) potassium iodide were added and stirring at 60° C. continued over night. After evaporation, 15 ml water was added and the mixture extracted with two portions of 15 ml ethyl acetate. The combined organic layers were washed with 1N sodium hydroxide and water, dried over sodium sulfate and evaporated to give 241 mg raw material which was purified on silica. Elution with ethyl acetate/methanol 5:1 yielded 88 mg (33%) 2-[(E)-2-(2-Fluoro-4-trifluoromethyl-phenyl)-vinyl]-4-[4-(4-imidazol-1-ylmethyl-thiazol-2-yl)-phenoxymethyl]-oxazole as off-white crystals melting at 133-135° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07259262B2
出典データセットuspto-grants-2007_08
ORD IDord-6734f8c080734d0c9bb3e586534c60f0
出典メモuspto-grants-2007_08