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HRID 42606作成日:2026年10月26日

Sodium Hydroxide → 6-(4-fluorophenyl)-5-(2-methylsulfanylpyrimidin-4-yl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/42606

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Phosphinic AcidHCID 4124402—
反応物Sodium NitriteHCID 23668193—
反応物HCID 178503413HCID 178503413—
溶媒Acetic AcidHCID 176—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
生成物6-(4-fluorophenyl)-5-(2-methylsulfanylpyrimidin-4-yl)-1H-pyrazolo[3,4-b]pyridineHCID 6701467742%

反応条件

温度0 °C

反応手順

To a solution of 3-amino-6-(4-fluorophenyl)-5-(2-methylsulfanylpyrimidin-4-yl)-1H-pyrazolo[3,4-b]pyridine (10.00 g, 28.4 mmol, obtained in example 180) in AcOH (52 mL), water (22 mL) and HCl conc. (5.7 mL), cooled to 0° C., a solution of NaNO2 (2.30 g, 33.4 mmol) in water (7.5 mL) was added dropwise. It was stirred for 30 min at 0° C., and H3PO2 (50% aqueous solution, 56.8 mL) was added slowly. It was stirred at 0° C. for 6 h. It was allowed to cool to room temperature, basified at 0° C. by slow addition of 6 N NaOH hasta pH=8 and was extracted with EtOAc. The combined organic phases were dried over Na2SO4 and concentrated to dryness. The crude product obtained was purified by chromatography on silica gel using hexane-EtOAc mixtures of increasing polarity as eluent, to afford 4.00 g of the title compound (yield: 42%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536194B2
出典データセットuspto-grants-2013_09
ORD IDord-36bc6544a1ae40ee983059e6b2d908c5
出典メモuspto-grants-2013_09