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m-Chloroperbenzoic acid → 6-Methanesulphonamido-2-methylquinoline-1-oxide

HRID 467104
ノート
印刷プレビュー

反応式

HRID 467104 の反応式
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH3:12][S:13]([NH:16][C:17]1[CH:18]=[C:19]2[C:24](=[CH:25][CH:26]=1)[N:23]=[C:22]([CH3:27])[CH:21]=[CH:20]2)(=[O:15])=[O:14]>C(Cl)Cl.C(=O)(O)[O-].[Na+]>[CH3:12][S:13]([NH:16][C:17]1[CH:18]=[C:19]2[C:24](=[CH:25][CH:26]=1)[N+:23]([O-:9])=[C:22]([CH3:27])[CH:21]=[CH:20]2)(=[O:14])=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 19813426N-(2-Methylquinolin-6-yl)methanesulfonamide

生成物 1

HCID 198134366-Methanesulphonamido-2-methylquinoline-1-oxide

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 516892Sodium Bicarbonate溶媒

実験手順

m-Chloroperbenzoic acid ("MCPBA") (5.2 g) was added portionwise to a solution of 6-methanesulphonamido-2-methylquinoline (6 g) in methylene chloride and stirring was continued for 17 hours. The reaction mixture was then diluted with aqueous sodium bicarbonate and the organic layer was separated. The aqueous layer was extracted with methylene chloride. The combined organic layers were washed with aqueous sodium bicarbonate, dried (MgSO4) and evaporated in vacuo to give a solid which was recrystallised from ethanol to give the title compound, yield 1.6 g, m.p. 241°-243°.

後処理

  1. customthe organic layer was separated
  2. extractionThe aqueous layer was extracted with methylene chloride
  3. washThe combined organic layers were washed with aqueous sodium bicarbonate
  4. dry with materialdried (MgSO4)
  5. customevaporated in vacuo
  6. customto give a solid which
  7. customwas recrystallised from ethanol

出典と根拠

ORDレコード
ord-d93894f0ebc546c89f1b63da77f6b7af
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05158964

反応ノート

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