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2-Methyl-5-piperazin-1-yl-quinoline → 5-{4-[2-(3-Bromophenyl)ethyl]-1-piperazinyl}-2-methylquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Methyl-5-piperazin-1-yl-quinoline | HCID 49851901 | — |
| 反応物 | 2-Methyl-5-(4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinoline | HCID 49851902 | — |
| 反応物 | Benzeneethanol, 3-bromo-, 1-methanesulfonate | HCID 57444273 | — |
| 生成物 | 5-{4-[2-(3-Bromophenyl)ethyl]-1-piperazinyl}-2-methylquinoline | HCID 57478284 | 56% |
反応手順
The title compound was prepared in 56% yield using a similar procedure to description D5 starting from 2-methyl-5-(1-piperazinyl)quinoline (D3) and 2-(3-bromophenyl)ethyl methanesulfonate (D13).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07732600B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-5db34a42240e480c884c3e96136bf5ea |
| 出典メモ | uspto-grants-2010_06 |