Water → 1-(3,4-dihydroquinolin-1(2H)-ylmethyl)-4-propylpyrrolidin-2-one

HRID 2043659ノート

反応式

HRID 2043659 の反応式
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1.[H-].[Na+].Cl[CH2:14][N:15]1[CH2:19][CH:18]([CH2:20][CH2:21][CH3:22])[CH2:17][C:16]1=[O:23].O>CN(C=O)C>[N:1]1([CH2:14][N:15]2[CH2:19][CH:18]([CH2:20][CH2:21][CH3:22])[CH2:17][C:16]2=[O:23])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1

参加物

6

反応物 4

HCID 962WaterHCID 24758Sodium hydrideHCID 694601,2,3,4-TetrahydroquinolineHCID 536292161-(Chloromethyl)-4-propylpyrrolidin-2-one

生成物 1

HCID 577430341-(3,4-dihydroquinolin-1(2H)-ylmethyl)-4-propylpyrrolidin-2-one収率 28%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

To a solution of 1,2,3,4-tetrahydroquinoline x158 (400 mg, 3 mmol, 1 eq) in DMF (7 ml) maintained under argon is added NaH (60% in mineral oil; 120 mg, 3 mmol, 1 eq). The reaction mixture is stirred for three hour at room temperature, then a solution of 1-(chloromethyl)-4-propylpyrrolidin-2-one x63 in DMF (1 M, 3 ml, 3 mmol, 1 eq) is added. The reaction mixture is stirred for 20 hours at the same temperature. Water (70 ml) is added and the resulting mixture is extracted with ethyl acetate (30 ml). The organic phase is washed twice with water and dried over Na2SO4. After filtration and evaporation, the crude product is purified by two consecutive chromatographies on silicagel (CH2Cl2/MeOH gradient, then CH2Cl2). Pure 1-(3,4-dihydroquinolin-1(2H)-ylmethyl)-4-propylpyrrolidin-2-one 295 is obtained as syrup (231 mg).

後処理

  1. stirringThe reaction mixture is stirred for 20 hours at the same temperature
  2. extractionthe resulting mixture is extracted with ethyl acetate (30 ml)
  3. washThe organic phase is washed twice with water
  4. dry with materialdried over Na2SO4
  5. filtrationAfter filtration and evaporation
  6. customthe crude product is purified by two consecutive chromatographies on silicagel (CH2Cl2/MeOH gradient

出典と根拠

ORDレコード
ord-f914a393db4943759e4ce5fd90e9a0c5
出典データセット
uspto-grants-2013_11
特許番号
US08586623B2

反応ノート

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