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Dimethyl Sulfoxide → 1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanone

HRID 216475
ノート
印刷プレビュー

反応式

HRID 216475 の反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[Br:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][C:19]2[C:20]([CH:29]([OH:35])[CH2:30][O:31][CH2:32][O:33][CH3:34])=[CH:21][C:22]3[NH:26][CH:25]=[N:24][C:23]=3[C:27]=2[F:28])=[C:14]([Cl:36])[CH:13]=1>C(Cl)Cl.O>[Br:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][C:19]2[C:20]([C:29](=[O:35])[CH2:30][O:31][CH2:32][O:33][CH3:34])=[CH:21][C:22]3[NH:26][CH:25]=[N:24][C:23]=3[C:27]=2[F:28])=[C:14]([Cl:36])[CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 679Dimethyl SulfoxideHCID 65578Oxalyl chlorideHCID 673451521-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanol

生成物 1

HCID 211141691-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanone

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒
3 回

実験手順

To a solution of oxalyl chloride (0.11 mL, 0.22 mmol) in CH2Cl2 (1 mL) at −78° C. is added DMSO (0.016 mL, 0.22 mmol). After stirring for 3 minutes, a solution of 1-[6-(4-bromo-2-chloro-phenylamino)-7-fluoro-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanol 10l (25 mg, 0.056 mmol) in methylene chloride (1 mL) is added. The resulting solution is stirred for 30 minutes at −78° C. TEA (0.1 mL, 0.71 mmol) is added. The reaction mixture is slowly warmed to room temperature, stirred for 5 minutes at room temperature, and diluted with water and CH2Cl2. The organic layer is separated, dried over MgSO4, filtered, and concentrated to give the crude product which is directly used without further purification.

後処理

  1. stirringThe resulting solution is stirred for 30 minutes at −78° C
  2. stirringstirred for 5 minutes at room temperature
  3. customThe organic layer is separated
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-3c43297cc1134f2a847e5c981c077288
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08193229B2

反応ノート

読み込み中…

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