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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 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]pyridine | HCID 67013805 | — |
| 生成物 | (1S)-N-(1-Phenylethyl)-[4-[6-[3-(trifluoromethyl)phenyl]-1H-pyrazolo[3,4-b]pyridin-5-yl]pyrimidin-2-yl]amine | HCID 68444827 | 16.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08536194B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-9ae7dc94d6e64c598e1c2a16aa26739f |
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| 出典メモ | uspto-grants-2013_09 |
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