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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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HRID 888122 반응식
[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
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참가 물질

3

반응물 1

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

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

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)
  • 출처 및 근거

    ORD 기록
    ord-89d481c879304da29116d892982aa88d
    출처 데이터셋
    uspto-grants-2012_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08247556B2

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