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HRID 220481作成日:2026年10月25日

Sodium hydride → 1-(3,5-Dimethylisoxazol-4-ylmethyl)-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/220481

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Isoxazole, 4-(chloromethyl)-3,5-dimethyl-HCID 88246—
反応物1H-pyrazole-4-carbaldehydeHCID 5130673—
溶媒DimethylformamideHCID 6228—
生成物1-(3,5-Dimethylisoxazol-4-ylmethyl)-1H-pyrazole-4-carbaldehydeHCID 86641653—

反応条件

温度0 °C

反応手順

Add N,N-dimethylformamide (3 mL) to sodium hydride (0.092 g, 2.29 mmol) and stir at 0° C. Add 1-H-pyrazole-4-carboxaldehyde (0.200 g, 2.08 mmol) and stir at 0° C. for 20 min. Dissolve 4-chloromethyl-3,5-dimethylisoxazole (0.318 g, 2.18 mmol) in N,N-dimethylformamide (4 mL) and add to reaction mixture. Stir reaction at room temperature for 18 hr. Quench with aqueous saturated sodium bicarbonate solution. Add ethyl acetate and separate organic layer. Extract aqueous layer twice with ethyl acetate. Dry combined organic layers (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 25:75 to 75:25 ethyl acetate:hexanes), to give the title preparation (387 mg, 91%). GC-MS: m/z=205 [M+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202873B2
出典データセットuspto-grants-2012_06
ORD IDord-b49960dd7d97476f83026d6423df702e
出典メモuspto-grants-2012_06