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1-(Methylsulphonyl)acetone → 6-Bromo-4-(4-fluoro-phenyl)-3-methanesulfonyl-2-methyl-quinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(Methylsulphonyl)acetone | HCID 78695 | — |
| 反応物 | (2-Amino-5-bromophenyl)(4-fluorophenyl)methanone | HCID 1359860 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 6-Bromo-4-(4-fluoro-phenyl)-3-methanesulfonyl-2-methyl-quinoline | HCID 12001719 | 28% |
反応手順
(2-Amino-5-bromo-phenyl)-(4-fluoro-phenyl)-methanone (compound of example A.1) (4 g, 14 mmol), methanesulfonylacetone (2.78 g, 20 mmol) and sodium tetrachloroaureate(III) dihydrate (0.27 g, 0.7 mmol) were heated at reflux in 2-propanol (50 ml) for 4 days. The resulting mixture was evaporated to dryness and the residue extracted with dichloromethane (2×), 1 N NaOH (2×) and NaCl (1×). The crude product was purified by chromatography in heptane/ethyl acetate with a gradient from 100:0 to 70:30. One obtained a light brown solid (1.5 g, 28%). MS: m/z=394 (M).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07728142B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-b053d5718d664bb6a9c72f5df8209328 |
| 出典メモ | uspto-grants-2010_06 |