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6-(4-Methylpiperazin-1-yl)pyridin-3-amine → 8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid [6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-amide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-(4-Methylpiperazin-1-yl)pyridin-3-amine | HCID 2763390 | — |
| 反応物 | 8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid | HCID 66914636 | — |
| 溶媒 | Dichloromethane methanol | HCID 21226129 | — |
| 生成物 | 8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid [6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-amide | HCID 44515978 | — |
反応手順
The title compound was prepared in analogy to the procedure described in Step 14.1 but stirring the reaction mixture for 20 h at rt, using 6-(4-methylpiperazin-1-yl)-pyridin-3-ylamine (prepared as described in Example 33 but using N-methyl-piperazine in Step 33.2) and 8-benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid (Example 59). Title compound: ESI-MS: 481.0 [M+H]+; tR=3.81 min (System 1); TLC: Rf=0.40 (DCM/MeOH, 9:1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08273882B2 |
| 出典データセット | uspto-grants-2012_09 |
| ORD ID | ord-93282a5cbf974232beffa12672538304 |
| 出典メモ | uspto-grants-2012_09 |