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HRID 253461作成日:2026年10月27日

Dimethylformamide → 2-fluoro-5-methoxy-4-(1-methyl-1H-benzimidazol-2-ylmethoxy)-benzaldehyde

https://huagongshe.com/reaction/253461

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物4-(1H-benzimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-benzaldehydeHCID 58086020—
生成物2-fluoro-5-methoxy-4-(1-methyl-1H-benzimidazol-2-ylmethoxy)-benzaldehydeHCID 5980387355%

反応手順

4-(1H-Benzimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-benzaldehyde (142) (0.600 g, 2.0 mmol) was dissolved in N,N-dimethylformamide (15 mL, 190 mmol). After the addition of sodium hydride (60% dispersion in oil, 0.072 g, 3.0 mmol) the reaction was stirred for 15 minutes at room temperature. Methyl iodide (140 μL, 2.2 mmol) was added dropwise to the mixture. The reaction was stirred overnight at room temperature under an atmosphere of nitrogen. The solvent was evaporated to dryness under reduced pressure. Ethyl acetate was added and the organic portion was washed with water, dried over anhydrous sodium sulfate and concentrated. Purification with silica gel flash chromatography with a gradient of ethyl acetate in hexanes gave the desired compound as a white powder (143, 0.345 g, 55%). MS (ESI) [M+H+]+=315.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872018B2
出典データセットuspto-grants-2011_01
ORD IDord-ed92e1fe79da49eaaf7820498ab0b543
出典メモuspto-grants-2011_01