Tetrahydrofuran → 8-Methoxy-1,2,3,4-tetrahydroisoquinoline

HRID 492634노트

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HRID 492634 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[C:11](=O)[NH:10][CH2:9][CH2:8]2.C1COCC1.[H-].[H-].[H-].[H-].[Li+].[Al+3].[OH-].[Na+]>O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[CH2:11][NH:10][CH2:9][CH2:8]2

참가 물질

6

실험 절차

Combine 8-Methoxy-3,4-dihydro-2H-isoquinolin-1-one (0.778 g, 4.40 mmol), THF (20 ml), and LiAlH4 (0.333 g, 8.8 mmol) at 0° C. under nitrogen atmosphere. After 30 minutes the reaction, reflux for 2 hours and then cool to room temperature. Quench the reaction by adding water and 1M NaOH at 0° C. and stirring for 12 hours at room temperature. Filter the reaction through celite and elute with THF. After concentrating the filtrate under reduced pressure, add the mixture to a 10 g SCX column pre-treated with 5% AcOH/MeOH. After rinsing several times with MeOH, elute the product using 1N NH3-MeOH followed by concentration under reduced pressure to afford 0.665 g, 4.07 mmol (93% yield) of the title compound as a tan oil: 1H NMR (500 MHz, CDCl3); 1.7-2.0 (1H, b s), 2.77 (2H, t, J=5.86), 3.09 (2H, t, J=5.86), 3.8 (3H, s), 3.95 (2H, s), 6.6-6.8 (2H, m), 7.0-7.15 (1H, m); TLC 5% MeOH: Ethyl acetate Rf:=0.1

후처리

  1. customat 0° C.
  2. customAfter 30 minutes the reaction
  3. temperaturereflux for 2 hours
  4. customQuench
  5. customthe reaction
  6. filtrationFilter
  7. customthe reaction through celite and
  8. washelute with THF
  9. concentrationAfter concentrating the filtrate under reduced pressure
  10. additionadd the mixture to a 10 g SCX column
  11. additionpre-treated with 5% AcOH/MeOH
  12. washAfter rinsing several times with MeOH
  13. washelute the product
  14. concentrationfollowed by concentration under reduced pressure

출처 및 근거

ORD 기록
ord-2dbf41a31bf943e2b0d6c0a85873a74c
출처 데이터셋
uspto-grants-2009_05
특허 번호
US07531557B2

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