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HRID 1865007作成日:2026年10月26日

Ethyl ketone → N-[2-Ethyl-4-methoxy-7-(2-methoxy-4,6-dimethylphenyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(1-ethylpropyl)amine

https://huagongshe.com/reaction/1865007

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl ketoneHCID 7288—
反応物Sodium HydroxideHCID 14798—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-Ethyl-4-methoxy-7-(2-methoxy-4,6-dimethylphenyl)pyrazolo[1,5-a]pyridin-3-amineHCID 21984791—
溶媒Acetic AcidHCID 176—
生成物N-[2-Ethyl-4-methoxy-7-(2-methoxy-4,6-dimethylphenyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(1-ethylpropyl)amineHCID 21984668—

反応手順

To a solution of 2-ethyl-4-methoxy-7-(2-methoxy-4,6-dimethylphenyl)pyrazolo[1,5-a]pyridin-3-amine (100 mg) in acetic acid (10 mL) there was added 3-pentanone (0.04 mL), and then sodium triacetoxyborohydride (85.0 mg) was slowly added at room temperature and the mixture was stirred for 3 hours. A 5 N aqueous sodium hydroxide solution was added while cooling on ice, and then extraction was performed with ethyl acetate, the organic layer washed with saturated aqueous sodium hydrogencarbonate and brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was subjected to silica gel column chromatography (10 g), and the title compound (69 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07625925B2
出典データセットuspto-grants-2009_12
ORD IDord-9b0e34d991ee4fb590ca967e38be7842
出典メモuspto-grants-2009_12