化工社化工社 化学情報印刷レポート · 研究参考用
1-(2-Methoxyphenyl)piperazine → isoquinolin-N-oxide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | AGN-PC-00GMS2 | HCID 11810396 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | isoquinolin-N-oxide | HCID 290378 | — |
反応手順
A mixture of 2.5g 4-chloromethyl-1-(3,4-dimethoxybenzyl-6,7-dimethoxyisoquinoline 2-oxide, 35 ml dimethylformamide, 1.8 triethylamine and 1.29 g 1-(2-methoxyphenyl)piperazine was stirred and heated under nitrogen at 50° for 7 hours. After evaporation of the solvent, the residue was partitioned between methylene chloride and water. The methylene chloride solution was washed with water and dried. After removal of the solvent in vacuo, the residue (3.5 g) was crystallized from methylene chloride/ethyl acetate to yield 3.05 g of yellow, hygroscopic crystals of 1-(3,4)-dimethoxybenzyl)-6,7-dimethoxy-4-{]4'-(2-methoxyphenyl)-1'-piperazinyl]methyl} isoquinoline 2-oxide, mp 128°-129° (dec.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04559403 |
| 出典データセット | uspto-grants-1985_12 |
| ORD ID | ord-a7652a369f1c41c3a08384f1bf64b0d4 |
| 出典メモ | uspto-grants-1985_12 |