関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| 反応物 | 1-Methylpiperazine | HCID 53167 | — |
| 生成物 | 1-Methyl-4-(3-nitrobenzyl)piperazine | HCID 1377109 | — |
反応手順
A mixture of 3-nitrobenzyl chloride (1 g) and N-methylpiperazine (3 ml) was stirred and heated to 100° C. for 4 hours. The mixture was cooled to ambient temperature and partitioned between methylene chloride and water. The organic phase was evaporated to give 3-(4-methylpiperazin-1-ylmethyl)nitrobenzene (1.05 g); NMR Spectrum: (DMSOd6) 2.14 (s, 3H), 2.31-2.38 (m, 8H), 3.57 (s, 2H), 7.6 (t, 1H), 7.54 (d, 1H), 8.07-8.13 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06548514B1 |
|---|
| 出典データセット | uspto-grants-2003_04 |
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| ORD ID | ord-15704b4784cc4f2ab644fad7b20edfdc |
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| 出典メモ | uspto-grants-2003_04 |
|---|