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HRID 1913673作成日:2026年10月26日

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

https://huagongshe.com/reaction/1913673

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物ChlorodifluoromethaneHCID 6372—
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-Difluoromethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880475—

反応手順

A mixture of 0.50 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 1.23 g of potassium carbonate and 14 ml of DMF was stirred while heating at 70° C. for three hours with chlorodifluoromethane gas injected. By stopping injection of gas, the mixture was cooled to room temperature and allowed to stand overnight. 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 0.11 g of 2-(3-difluoromethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 126”).

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-74df6f667add46f188820196f37c26df
出典メモuspto-grants-2013_12