関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetramethyltin | HCID 11661 | — |
| 反応物 | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| 反応物 | 4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979972 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-(4-Methyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979807 | — |
反応手順
A solution of Intermediate 71 (313 mg) in toluene (6 ml) was added with tetrakis(triphenylphosphine)palladium(0) (17.9 mg, Aldrich), tetramethyltin (165 μl, Kanto Chemicals) and 2,6-di-tert-butyl-4-methylphenol (several pellets, Tokyo Kasei Kogyo) and stirred in a sealed tube at 150° C. for 48 hours. The reaction mixture was cooled to room temperature, filtered through Celite and concentrated under reduced pressure. The residue was added with saturated brine (30 ml) and extracted three times with ethyl acetate (30 ml for each time). The organic layers were combined and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain the title compound (61.7 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07094789B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-2e9115487cd940a38efae8fd5e24df8a |
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| 出典メモ | uspto-grants-2006_08 |
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