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Triethylamine → 1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Propanol, 1-amino-2-methyl- | HCID 95102 | — |
| 反応物 | 7-Benzyl-4-chloro-3-nitroquinoline | HCID 21984193 | — |
| 反応物 | 6-Benzyl-4-chloro-3-nitroquinoline | HCID 21984226 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984410 | — |
| 生成物 | 1-(7-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984452 | — |
反応手順
Under a nitrogen atmosphere, 1-amino-2-methylpropan-2-ol (1.2 equivalents) was added to a 0.2 M solution of 7-benzyl-4-chloro-3-nitroquinoline or 6-benzyl-4-chloro-3-nitroquinoline (1 equivalent) and triethylamine (3 equivalents) in dichloromethane, and the reaction was stirred overnight at ambient temperature. The volatiles were removed under reduced pressure, and the residue was stirred with water (50 mL) for one hour. The resulting yellow solid was isolated by filtration and washed with water to provide 1-(7-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(6-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol, respectively.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091214B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-a26247a753df407cb8aa5733bcc350c4 |
| 出典メモ | uspto-grants-2006_08 |