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HRID 42599作成日:2026年10月24日

1-Phenethylamine, (-)- → (1S)-N-(1-Phenylethyl)-[4-[6-[3-(trifluoromethyl)phenyl]-1H-pyrazolo[3,4-b]pyridin-5-yl]pyrimidin-2-yl]amine

https://huagongshe.com/ja/reaction/42599

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenethylamine, (-)-HCID 75818—
反応物5-[2-(methylsulfonyl)pyrimidin-4-yl]-6-[3-(trifluoromethyl)phenyl]-1H-pyrazolo[3,4-b]pyridineHCID 67013805—
生成物(1S)-N-(1-Phenylethyl)-[4-[6-[3-(trifluoromethyl)phenyl]-1H-pyrazolo[3,4-b]pyridin-5-yl]pyrimidin-2-yl]amineHCID 6844482716.7%

反応条件

温度100 °C

反応手順

A mixture of 5-[2-(methylsulfonyl)pyrimidin-4-yl]-6-[3-(trifluoromethyl)phenyl]-1H-pyrazolo[3,4-b]pyridine (0.55 g, 0.13 mmol, obtained in example 127) and (1S)-1-phenylethylamine (0.16 g, 1.3 mmol) was heated to 100° C. for 1 h. It was allowed to cool and the crude product obtained was purified by chromatography on silica gel using increasing polarity mixtures of EtOAc-hexane as eluent, to afford 10 mg of the title compound (yield: 16%).

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-9ae7dc94d6e64c598e1c2a16aa26739f
出典メモuspto-grants-2013_09