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(7-Bromo-3-nitroquinolin-4-yl)isobutylamine → 7-bromo-N4-isobutylquinoline-3,4-diamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (7-Bromo-3-nitroquinolin-4-yl)isobutylamine | HCID 21984282 | — |
| 触媒 | Platinum | HCID 23939 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 7-bromo-N4-isobutylquinoline-3,4-diamine | HCID 68818159 | — |
反応手順
A solution of (7-bromo-3-nitroquinolin-4-yl)-(2-methylpropyl)amine (30.9 g, 105 mmol) in acetonitrile (1.8 L) and isopropanol (200 mL) was added to a Parr vessel. A mixture of 5% platinum on carbon (3.0 g) and acetonitrile:isopropanol (20 mL) was added, and the vessel was purged with nitrogen. The vessel was placed under hydrogen pressure (40 psi, 2.8×105 Pa) for two hours. After one hour, the pressure had decreased to 20 psi (1.4×105 Pa) and was readjusted to 40 psi (2.8×105 Pa). The reaction mixture was filtered through a layer of CELITE filter aid, and the filter cake was washed with acetonitrile. The filtrate was concentrated under reduced pressure to provide 7-bromo-N4-(2-methylpropyl)quinoline-3,4-diamine as an oil.
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-aae0dad34e834b03a63c256ec63dadca |
| 出典メモ | uspto-grants-2006_08 |