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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 582021생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,4-Difluorobenzyl alcoholHCID 91867—
반응물4-Cyano-2.6-bis(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridineHCID 54060249—
용매SulfolaneHCID 31347—
용매Ethyl acetate pentaneHCID 22335286—
생성물4-Cyano-6-(2,4-difluorobenzyloxy)-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)pyridineHCID 5394696521.2%

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05922738
출처 데이터셋uspto-grants-1999_07
ORD IDord-2dc9f3a0f29348f887ce316afa20cb33
출처 메모uspto-grants-1999_07