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HRID 1621447作成日:2026年10月25日

Water → 6-(2-fluoro-5-vinylpyridin-3-yl)-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purine

https://huagongshe.com/reaction/1621447

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium AcetateHCID 517044—
反応物6-chloro-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 59548268—
反応物2-Fluoro-5-vinylpyridin-3-ylboronic acidHCID 59548347—
触媒HCID 178482906HCID 178482906—
溶媒EthanolHCID 702—
生成物6-(2-fluoro-5-vinylpyridin-3-yl)-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 59548434—

反応条件

温度80 °C

反応手順

6-Chloro-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (984 mg, 3.89 mmol), 2-fluoro-5-vinylpyridin-3-ylboronic acid (882 mg, 5.28 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphino)dichloropalladium (138 mg, 0.195 mmol), and potassium acetate (1.212 g, 12.35 mmol) were suspended in ethanol (12.0 mL) and water (2.4 mL) and the flask was fitted with a reflux condenser and nitrogen was bubbled through the suspension for about 15 seconds. Then, the flask was put in a preheated oil bath (80° C.) and stirred under nitrogen for 1 h. The reaction was cooled to room temperature, diluted with water (20 mL), and extracted with DCM. The organic extracts were combined, dried over sodium sulfate, filtered, concentrated, and purified on a silica gel column (25:1 to 20:1 DCM/2N ammonia in MeOH) to afford 6-(2-fluoro-5-vinylpyridin-3-yl)-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purine, which was taken on to the next step. MS (ESI pos. ion) m/z 340 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08772480B2
出典データセットuspto-grants-2014_07
ORD IDord-3669b0edee01487081d4442d20857cba
出典メモuspto-grants-2014_07