関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-(Aminomethyl)cyclopentan-1-ol | HCID 13051202 | — |
| 反応物 | 7-Bromo-4-chloro-3-nitro[1,5]naphthyridine | HCID 57457837 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 1-{[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanol | HCID 67052453 | — |
反応手順
A suspension of 7-bromo-4-chloro-3-nitro[1,5]naphthyridine (54.42 g, 188.6 mmol) in chloroform (820 mL) was cooled to 0° C., and triethylamine (105 mL, 755 mmol) was added. A solution of 1-(aminomethyl)cyclopentanol (28.25 g, 245.2 mmol) in chloroform (272 mL) was added slowly over a period of 15 minutes. The reaction was allowed to warm to room temperature and stirred for 30 minutes. The solution was washed sequentially with water (500 mL) and saturated aqueous sodium bicarbonate (750 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 1-{[(7-bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07897609B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-c3aa6b0b83bb485ca8fb2bfacae7a3f6 |
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| 出典メモ | uspto-grants-2011_03 |
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