Cesium carbonate → Methyl 4-{[2-(dimethylamino)ethyl]amino}benzoate

HRID 16753

反応式

HRID 16753 の反応式
I[C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[CH3:12][N:13]([CH3:17])[CH2:14][CH2:15][NH2:16].C(=O)([O-])[O-].[Cs+].[Cs+].C(C1CCCCC1=O)(=O)C>CN(C)C=O.[Cu]I>[CH3:12][N:13]([CH3:17])[CH2:14][CH2:15][NH:16][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1

参加物

7

反応物 4

HCID 10796Cesium carbonateHCID 134002-AcetylcyclohexanoneHCID 66053N,N-DimethylethylenediamineHCID 69273Methyl 4-iodobenzoate

生成物 1

HCID 57440398Methyl 4-{[2-(dimethylamino)ethyl]amino}benzoate収率 99.1%

試薬・触媒・溶媒 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

Methyl 4-iodobenzoate (1.19 g, 4.54 mmol, 1.0 eq) was dissolved in dry dimethylformamide (10 ml). N,N-dimethylethane-1,2-diamine (400 mg, 4.54 mmol, 1.0 eq), caesium carbonate (2.69 g, 9.08 mmol, 2.0 eq), 2-acetylcyclohexanone (120 μl, 0.908 mmol, 0.20 eq [20 mol %]) and copper (I) iodide (44 mg, 0.227 mmol, 0.05 eq [5 mol %]) were added and the mixture was stirred under nitrogen at 90° C. for 18 h. The reaction mixture was concentrated, dissolved in methanol and absorbed onto a SCX-2 cation exchange resin column. The column was washed with methanol and the product was eluted with 2M ammonia in methanol. Fractions were evaporated to give methyl 4-(2-[dimethylamino]ethylamino)benzoate (1.00 g, 99%) as a brown gum.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. dissolutiondissolved in methanol
  3. customabsorbed onto a SCX-2 cation exchange resin column
  4. washThe column was washed with methanol
  5. washthe product was eluted with 2M ammonia in methanol
  6. customFractions were evaporated

出典と根拠

ORDレコード
ord-a10a6137de684c51aac6344846716ae5
出典データセット
uspto-grants-2010_06
特許番号
US07737149B2

関連ノート

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