Sodium Iodide → HCID 17830867、化合物

HRID 478367ノート

反応式

HRID 478367 の反応式
[CH3:1][C:2]1[CH:20]=[C:19]([NH:21][C:22](=[O:25])[CH2:23]Cl)[CH:18]=[CH:17][C:3]=1[C:4]([N:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:5].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[C:34]1([OH:44])[C:43]2[CH2:42][CH2:41][CH2:40][CH2:39][C:38]=2[CH:37]=[CH:36][CH:35]=1>CN(C)C=O.C(OCC)(=O)C>[CH3:1][C:2]1[CH:20]=[C:19]([NH:21][C:22](=[O:25])[CH2:23][O:44][C:34]2[CH:35]=[CH:36][CH:37]=[C:38]3[C:43]=2[CH2:42][CH2:41][CH2:40][CH2:39]3)[CH:18]=[CH:17][C:3]=1[C:4]([N:6]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:5]

参加物

7

反応条件

温度
60 °C

実験手順

1-[2-Methyl-4-(2-chloroacetylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.8 g) is dissolved in dimethylformamide (5 ml), and thereto are added potassium carbonate (0.47 g), sodium iodide (0.51 g) and 5,6,7,8-tetrahydro-1-naphthol (0.40 g), and the mixture is stirred at 60° C. for three hours. To the reaction solution is added ethyl acetate, and the mixture is washed with a saturated aqueous potassium hydrogen sulfate solution and a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated. The resulting residue is allowed to stand for one day, washed with dichloromethane, filtered, and dried to give 1-{2-methyl-4-[2-(5-tetrahydronaphthyloxy)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzazepine (0.72 g) as white powder.

後処理

  1. washthe mixture is washed with a saturated aqueous potassium hydrogen sulfate solution
  2. dry with materiala saturated aqueous sodium chloride solution, dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. waitto stand for one day
  6. washwashed with dichloromethane
  7. filtrationfiltered
  8. customdried

出典と根拠

ORDレコード
ord-215a1deb875342d09aaea70357d61ab1
出典データセット
uspto-grants-2003_11
特許番号
US06642223B2

反応ノート

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