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HRID 15296作成日:2026年10月26日
4-(N-Boc-amino)piperidine → Methyl 3-[4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-1-piperidinyl]-2-[6-(methyloxy)-1,5-naphthyridin-4-yl]propanoate
https://huagongshe.com/reaction/15296
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| 反応物 | Methyl 2-[6-(methyloxy)-1,5-naphthyridin-4-yl]-2-propenoate | HCID 57423102 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| 生成物 | Methyl 3-[4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-1-piperidinyl]-2-[6-(methyloxy)-1,5-naphthyridin-4-yl]propanoate | HCID 57423104 | — |
反応手順
To a solution of methyl 2-[6-(methyloxy)-1,5-naphthyridin-4-yl]-2-propenoate (2.53 g, 10.37 mmol) in DMF (4 ml) and tetramethylguanidine (0.1 ml) was added 1,1-dimethylethyl 4-piperidinylcarbamate (2.08 g, 10.37 mmol). The reaction was stirred for 1 hour at 70° C. after which time the solvent was evaporated. The residue was chromatographed on silica eluting with a gradient of 5% methanol in dichloromethane affording the desired compound as a yellow solid (2.66 g, 58%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07732461B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-3cf1206945f44fc7be4f7d9f075c1ab8 |
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| 出典メモ | uspto-grants-2010_06 |
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