Benzoyl chloride → N-(4-benzyl-4-dimethylaminocyclohexyl)-N-propylbenzamide hydrochloride

HRID 1179035ノート

反応式

HRID 1179035 の反応式
[CH2:1]([C:8]1([N:18]([CH3:20])[CH3:19])[CH2:13][CH2:12][CH:11]([NH:14][CH2:15][CH2:16][CH3:17])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:28]([Cl:36])(=[O:35])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.[OH-].[K+]>C(Cl)Cl.CN(C)C1C=CN=CC=1.O>[ClH:36].[CH2:1]([C:8]1([N:18]([CH3:20])[CH3:19])[CH2:13][CH2:12][CH:11]([N:14]([CH2:15][CH2:16][CH3:17])[C:28](=[O:35])[C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

8

実験手順

700 mg of the nonpolar diastereomer of 1-benzyl-N,N-dimethyl-N′-propyl-cyclohexane-1,4-diamine were dissolved in 10 ml methylene chloride, and 370 μl triethylamine and approx. 10 mg DMAP (4-dimethylaminopyridine) were added. 311 μl benzoyl chloride were added dropwise, while cooling in an ice/methanol bath, and the reaction mixture was then stirred overnight, while warming to room temperature. For working up, 10 ml five molar KOH solution and 10 ml water were added, the mixture was stirred for ten minutes and extracted three times with 20 ml methylene chloride each time, the combined extracts were dried over magnesium sulfate and filtered and the filtrate was concentrated. From the crude product obtained (834 mg), 909 mg N-(4-benzyl-4-dimethylamino-cyclohexyl)-N-propyl-benzamide hydrochloride were prepared as described for example 1 with water and chlorotrimethylsilane in 2-butanone.

後処理

  1. temperaturewhile cooling in an ice/methanol bath
  2. stirringthe mixture was stirred for ten minutes
  3. extractionextracted three times with 20 ml methylene chloride each time
  4. dry with materialthe combined extracts were dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-a2e120059db54a5a8a7c170f8420c055
出典データセット
uspto-grants-2007_10
特許番号
US07276518B2

反応ノート

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