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HRID 510110作成日:2026年10月27日
2-Chloro-7H-pyrrolo[2,3-d]pyrimidine → 5-Fluoro-1-(2-fluorobenzyl)-3-(7H-pyrrolo[2,3-d]pyrimidin-2-yl)-1H-pyrazolo[3,4-b]pyridine
https://huagongshe.com/reaction/510110
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Chloro-7H-pyrrolo[2,3-d]pyrimidine | HCID 5706774 | — |
| 反応物 | 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine | HCID 58065602 | — |
| 反応物 | HCID 178448238 | HCID 178448238 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 5-Fluoro-1-(2-fluorobenzyl)-3-(7H-pyrrolo[2,3-d]pyrimidin-2-yl)-1H-pyrazolo[3,4-b]pyridine | HCID 66614193 | — |
反応手順
Under an argon atmosphere, 2.000 g (5.389 mmol) of the compound from example 24A were dissolved in 200 ml of 1,4-dioxane, and 9.378 g (16.167 mmol) of hexabutyldistannane were added. Added to the mixture were 2.000 g (1.731 mmol) of tetrakis(triphenylphosphine)palladium(0) and 0.910 g (5.928 mmol) of 2-chloro-7H-pyrrolo[2,3-d]pyrimidine (described in Bioorg. Med. Chem. 17(19), 6926-6936; 2009). The mixture was heated to reflux for 60 h. After cooling, the reaction mixture was filtered through Celite and the filtrate was concentrated on a rotary evaporator. The residue was stirred successively with ethyl acetate, acetonitrile and dimethyl sulfoxide. Subsequently, the residue was dissolved in trifluoroacetic acid, and acetonitrile and water were added until slight turbidity. The mixture was filtered and the filtrate was concentrated on a rotary evaporator and the residue was dried under high vacuum. 161 mg (8% of theory) of the title compound were obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09096592B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-764991be8e434bd8a4cf8f0ea7c7308d |
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| 出典メモ | uspto-grants-2015_08 |
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