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HRID 13674作成日:2026年10月25日

1-(Methylsulphonyl)acetone → 6-Bromo-3-methanesulfonyl-2-methyl-4-(2,4,5-trifluoro-phenyl)-quinoline

https://huagongshe.com/reaction/13674

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Methylsulphonyl)acetoneHCID 78695—
反応物SodiumHCID 5360545—
反応物(2-Amino-5-bromo-phenyl)-(2,4,5-trifluoro-phenyl)-methanoneHCID 12001620—
溶媒IsopropanolHCID 3776—
生成物6-Bromo-3-methanesulfonyl-2-methyl-4-(2,4,5-trifluoro-phenyl)-quinolineHCID 1200172620.4%

反応手順

(2-Amino-5-bromo-phenyl)-(2,4,5-trifluoro-phenyl)-methanone (compound of example A.4) (1.9 g, 5.7 mmol), methanesulfonylacetone (1.18 g, 8.6 mmol) and sodium tetrachloroaureate(III) dihydrate (0.12 g, 0.28 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×), NaOH (2×) and NaCl (1×). The crude product was purified by chromatography on silica gel with a heptane/ethyl acetate gradient from 100:0 to 90:10. One obtained a light yellow solid (0.5 g, 20%). MS: m/z=430 (M).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728142B2
出典データセットuspto-grants-2010_06
ORD IDord-3a85f4b8f3cc4a6f9babee2cbeed1283
出典メモuspto-grants-2010_06