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7-Amino-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one → 4,4-Dimethyl-1,2,3,4-tetrahydroquinolin-7-amine

HRID 888122
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反応式

HRID 888122 の反応式
[NH2:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([CH3:14])([CH3:13])[CH2:7][C:8](=O)[NH:9]2)=[CH:4][CH:3]=1>C1COCC1>[CH3:13][C:6]1([CH3:14])[C:5]2[C:10](=[CH:11][C:2]([NH2:1])=[CH:3][CH:4]=2)[NH:9][CH2:8][CH2:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 144764787-Amino-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

生成物 1

HCID 219614824,4-Dimethyl-1,2,3,4-tetrahydroquinolin-7-amine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of 7-amino-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (1.07 g, 5.62 mmol) and borane dimethylsulfide complex (1.60 ml, 16.9 mmol) in 40 ml of anhydrous THF was heated at reflux under N2 for 15 h. The solvents were removed under reduced pressure. The residue was heated at reflux in 20 ml of MeOH for 2 h, then 0.80 g of NaHCO3 was added, and the mixture was heated at reflux for 2 h. The mixture was filtered, condensed, and the residue was purified by flash column chromatography (5 to 10% of EtOAc in CH2Cl2). The titled compound was obtained as a viscous oil. MS(ES+): 176.9 (M+H)+. Calc'd for C11H16N—176.26.

後処理

  1. temperature
was heated
  • temperatureat reflux under N2 for 15 h
  • customThe solvents were removed under reduced pressure
  • temperatureThe residue was heated
  • temperatureat reflux in 20 ml of MeOH for 2 h
  • addition0.80 g of NaHCO3 was added
  • temperaturethe mixture was heated
  • temperatureat reflux for 2 h
  • filtrationThe mixture was filtered
  • customcondensed
  • customthe residue was purified by flash column chromatography (5 to 10% of EtOAc in CH2Cl2)
  • 出典と根拠

    ORDレコード
    ord-89d481c879304da29116d892982aa88d
    出典データセット
    uspto-grants-2012_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08247556B2

    反応ノート

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