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8-Quinolinamine, 6-bromo- → 5-Acetyl-4-[(6-bromoquinolin-8-yl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 8-Quinolinamine, 6-bromo- | HCID 93637 | — |
| 反応物 | 5-acetyl-2-ethylnitro6-phenylpyridazin-3(2H)-one | HCID 10732015 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-Acetyl-4-[(6-bromoquinolin-8-yl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one | HCID 68485649 | 85.3% |
反応手順
To a stirred solution of 80 mg (0.279 mmol) of 5-acetyl-2-ethyl-4-nitro-6-phenylpyridazin-3(2H)-one (Dal Piaz, V et al, J. Med. Chem. 1997, 40, 1417) in ethanol (4 mL), 8-amino-6-bromoquinoline (93 mg, 0.417 mmol) was added. The resulting mixture was stirred at room temperature or one day. The solvent was evaporated and the residue purified by column chromatography (silica gel, hexane/ethyl acetate 3:1) to yield the title compound (110 mg, 85.3% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07491722B2 |
| 出典データセット | uspto-grants-2009_02 |
| ORD ID | ord-11ca5e69572648439f9b95e2087dbef5 |
| 出典メモ | uspto-grants-2009_02 |