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(2E)-3-(4-Chlorophenyl)acryloyl chloride → (2E)-3-(4-chlorophenyl)-N-(2-piperidin-1-ylquinolin-6-yl)prop-2-enamide hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2E)-3-(4-Chlorophenyl)acryloyl chloride | HCID 11252649 | — |
| 反応物 | Quinoline-2,6-diamine | HCID 22018948 | — |
| 反応物 | 2-Piperidin-1-ylquinolin-6-amine | HCID 22018974 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (2E)-3-(4-chlorophenyl)-N-(2-piperidin-1-ylquinolin-6-yl)prop-2-enamide hydrochloride | HCID 22018962 | — |
反応手順
To a solution of the product of Step D (91 mg, 0.4 mmol) in 2 mL HOAc was added the product of Step E (64 mg, 0.32 mmol). The resulting mixture was stirred at r.t. for 3 h then diluted with 3 mL ether. The resulting mixture was filtered and the resulting solids were washed with ether. The solids were dried under vacuum to afford the product, MS: m/z 392 (MH+), as an off-white solid. Using the appropriate starting materials and following procedures similar to those described above for Example 1, the following compounds were prepared from the corresponding quinoline-2,6-diamine intermediates:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084156B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-7ea16d5540f64108a374fefb1059f324 |
| 出典メモ | uspto-grants-2006_08 |