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1-(Methylsulphonyl)acetone → 6-Bromo-4-(4-chloro-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-chlorophenyl)methanone | HCID 182477 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 6-Bromo-4-(4-chloro-phenyl)-3-methanesulfonyl-2-methyl-quinoline | HCID 12001721 | 19% |
反応手順
(2-Amino-5-bromo-phenyl)-(4-chloro-phenyl)-methanone (compound of example A.2) (4 g, 12.9 mmol), methanesulfonylacetone (2.63 g, 19.3 mmol) and sodium tetrachloroaureate(III) dihydrate (0.26 g, 0.64 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 sat. NaCl (1×). The crude product was purified by chromatography on silica gel in dichloromethane. The product was crystallized from dichloromethane/heptane by evaporation of dichloromethane. One obtained a light yellow solid (1 g, 19%). MS: m/z=410 (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-2e6422c6666e4cd8adb388d13ca64956 |
| 出典メモ | uspto-grants-2010_06 |