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HRID 582021作成日:2026年10月24日

Sodium hydride → 4-Cyano-6-(2,4-difluorobenzyloxy)-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridine

https://huagongshe.com/ja/reaction/582021

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2,4-Difluorobenzyl alcoholHCID 91867—
反応物4-Cyano-2.6-bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridineHCID 54060249—
溶媒SulfolaneHCID 31347—
溶媒Ethyl acetate pentaneHCID 22335286—
生成物4-Cyano-6-(2,4-difluorobenzyloxy)-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridineHCID 5394696521.2%

反応条件

温度90 °C

反応手順

Sodium hydride (0.1 g, 60%, 2.5 mmol) is added to a solution of 2,4-difluorobenzyl alcohol (0.28 ml, 2.5 mmol) in sulfolane (5 ml) at 50° C. After 1 hour at 50° C., 4-cyano-2,6-bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridine (1 g, 2.3 mmol) (from Example 2) is added to the reaction mixture. The mixture is heated to 90° C. overnight. After cooling, the reaction mixture is diluted with pentane/ethyl acetate (by volume ration 1/1) and filtered through a bed of silica gel. The filtrate is washed 6 times with water. The organic layer is dried with anhydrous magnesium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (silica gel: pentane/ethyl acetate 8/2 v/v) and washing of the product with diisopropyl ether yields the title compound (0.2 g, 21% yield) of melting point 109° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05922738
出典データセットuspto-grants-1999_07
ORD IDord-2dc9f3a0f29348f887ce316afa20cb33
出典メモuspto-grants-1999_07