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HRID 1864991作成日:2026年10月27日

1,2-Dibromoethane → 7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1864991

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DibromoethaneHCID 7839—
反応物Ammonium ChlorideHCID 25517—
反応物2-Ethyl-4-methoxypyrazolo[1,5-a]pyridineHCID 21984578—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridineHCID 21984567—

反応条件

温度-78 °C

反応手順

n-Butyllithium (1.31 mL) was slowly added dropwise to a solution of 2-ethyl-4-methoxypyrazolo[1,5-a]pyridine (303 mg) in tetrahydrofuran (15 mL) at −78° C. After stirring the mixture at −78° C. for 1 hour, 1,2-dibromoethane (0.18 mL) was added and stirring was continued for 1 hour. Saturated aqueous ammonium chloride was added, extraction was performed with ethyl acetate, the extract washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (20 g), and the title compound (282 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a colorless oil.

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-36c761d88e6d4f768136cecaec694884
出典メモuspto-grants-2009_12