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4-Aminopyridazine → 5-cyclopentyl-N-pyridazin-4-yl-6-(2,2,2-trifluoro-ethoxy)-nicotinamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Aminopyridazine | HCID 298492 | — |
| 反応物 | 5-Cyclopentyl-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acid | HCID 71294186 | — |
| 生成物 | 5-cyclopentyl-N-pyridazin-4-yl-6-(2,2,2-trifluoro-ethoxy)-nicotinamide | HCID 71294494 | — |
反応手順
This compound was prepared following the same procedure as described in Example 11 using 5-cyclopentyl-6-(2,2,2-trifluoro-ethoxy)-nicotinic acid (Example 9c) (100 mg, 0.35 mmol) and 4-pyridazinamine (CAN 20744-39-2, 39.5 mg, 0.41 mmol) as starting materials; off white solid (12 mg, 9.5%). MS (ESI): 367.2 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08629166B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-a0995aaab2cc4c299a2fd5e1d071176f |
| 出典メモ | uspto-grants-2014_01 |