4-Amino-m-cresol → 3-Butyryl-4-(4-hydroxy-2-methylphenylamino)-8-acetylquinoline

HRID 1885174ノート

反応式

HRID 1885174 の反応式
[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1Cl)=[CH:13][CH:12]=[CH:11][C:10]=2[C:17](=[O:19])[CH3:18])(=[O:5])[CH2:2][CH2:3][CH3:4].[NH2:20][C:21]1[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][C:22]=1[CH3:28]>O1CCOCC1>[C:1]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:20][C:21]1[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][C:22]=1[CH3:28])=[CH:13][CH:12]=[CH:11][C:10]=2[C:17](=[O:19])[CH3:18])(=[O:5])[CH2:2][CH2:3][CH3:4]

参加物

4

反応物 2

HCID 178194-Amino-m-cresolHCID 102654513-Butyryl-4-chloro-8-acetylquinoline

生成物 1

HCID 100900403-Butyryl-4-(4-hydroxy-2-methylphenylamino)-8-acetylquinoline収率 24.7%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A solution of 3-butyryl-4-chloro-8-acetylquinoline (2.0 g) and 4-amino-3-methylphenol (1.23 g, 10 mmol) in 1,4-dioxan (25 ml) was warmed briefly to reflux, then the dioxan evaporated. Chromatography (silica, 4-6% methanol in dichloromethane) and recrystallisation from ethyl acetate gave 3-butyryl-4-(4-hydroxy-2-methylphenylamino)-8-acetylquinoline (0.65 g), m.p. 183°-185°.

後処理

  1. temperatureto reflux
  2. customthe dioxan evaporated
  3. customChromatography (silica, 4-6% methanol in dichloromethane) and recrystallisation from ethyl acetate

出典と根拠

ORDレコード
ord-020611f96fff4f0b8ad22713ed6e76b1
出典データセット
uspto-grants-1992_09
特許番号
US05143920

反応ノート

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