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HRID 13667作成日:2026年10月25日

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

https://huagongshe.com/reaction/13667

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(2-Amino-5-bromophenyl)(4-fluorophenyl)methanoneHCID 1359860—
反応物SodiumHCID 5360545—
溶媒IsopropanolHCID 3776—
生成物6-Bromo-4-(4-fluoro-phenyl)-3-methanesulfonyl-2-methyl-quinolineHCID 1200171928%

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

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-b053d5718d664bb6a9c72f5df8209328
出典メモuspto-grants-2010_06