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HRID 1181906作成日:2026年10月27日

Water → N-[7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(2-pyridyl)amine

https://huagongshe.com/reaction/1181906

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-BromopyridineHCID 7973—
反応物7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridine-3-amineHCID 21984486—
反応物Sodium t-butoxideHCID 23676156—
溶媒TolueneHCID 1140—
生成物N-[7-(2-Methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(2-pyridyl)amineHCID 21984615—

反応条件

温度120 °C

反応手順

After dissolving [7-(2-methoxy-4,6-dimethylphenyl)-2-(methylsulfanyl)pyrazolo[1,5-a]pyridin-3-yl]amine (40 mg) in toluene (1 mL), 2-bromopyridine (0.013 mL), sodium t-butoxide (25 mg) and dichlorobis(tri-o-tolylphosphine)palladium complex (3 mg) were added and the mixture was heated and stirred at 120° C. for 5 hours. The mixture was cooled to room temperature, water was added, and extraction was performed with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography, and the title compound (12 mg) was obtained from the ethyl acetate:n-hexane (1:2) fraction as white crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07285666B2
出典データセットuspto-grants-2007_10
ORD IDord-2c125486dbe44dd69df42bb5c4ab0fb4
出典メモuspto-grants-2007_10