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3-Fluoro-4-(4-methylpiperazin-1-yl)aniline → 1-(2-Fluoro-4-isothio-cyanatophenyl)-4-methylpiperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Fluoro-4-(4-methylpiperazin-1-yl)aniline | HCID 2783055 | — |
| 反応物 | Thiocarbonyl diimidazole | HCID 11412697 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-(2-Fluoro-4-isothio-cyanatophenyl)-4-methylpiperazine | HCID 9942978 | — |
反応手順
Thiocarbonyl diimidazole (3.00 g, 3.53 mmol) (Aldrich) was dissolved in N,N-dimethylformamide (10 mL) and the solution was cooled to −10° C. (ice/acetone bath). A solution of 3-fluoro-4-(4-methyl-1-piperazinyl) benzenamine (2.26 g, 10.8 mmol) (from Step B above) in N,N-dimethylformamide (30 mL) was added over a period of 30 minutes, then the cooling bath was removed and the solution was stirred overnight. Ice-water was then added (100 mL) and the mixture was extracted with ether (3×200 mL). The combined ether layers were dried (MgSO4), filtered, and evaporated to give 1-(2-fluoro-4-isothio-cyanatophenyl)-4-methylpiperazine as a yellow oil that solidified on standing (3.88 g, 92%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07094896B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-8e88da186bb64330afe884ecd3c3eb32 |
| 出典メモ | uspto-grants-2006_08 |