戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1913671作成日:2026年10月27日

Dimethylformamide → 2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/1913671

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物BromocyclopentaneHCID 8728—
反応物Potassium CarbonateHCID 11430—
反応物4-[5-(Trifluoromethyl)benzoxazole-2-yl]pyridin-3-olHCID 136331268—
溶媒WaterHCID 962—
生成物2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688022083.3%

反応条件

温度60 °C

反応手順

To a mixture of 0.28 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 0.28 g of potassium carbonate and 2 ml of DMF, a mixture of 0.29 g of cyclopentyl bromide and 2 ml of DMF was added at room temperature. The reaction mixture was stirred while heating at 60° C. for four hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.29 g of 2-(3-cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 115”).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609705B2
出典データセットuspto-grants-2013_12
ORD IDord-6ba03f1821ac4b9aa8bc2a75d6dac585
出典メモuspto-grants-2013_12