Phosphorus oxychloride → 1-Methyl-5,6,7-trimethoxy-3,4-dihydroisoquinoline

HRID 1647316Notes

Reaction equation

HRID 1647316 reaction equation
[CH3:1][O:2][C:3]1[C:14]([O:15][CH3:16])=[C:13]([O:17][CH3:18])[CH:12]=[CH:11][C:4]=1[CH2:5][CH2:6][NH:7][C:8](=O)[CH3:9].O=P(Cl)(Cl)Cl>C1(C)C=CC=CC=1>[CH3:9][C:8]1[C:11]2[C:4](=[C:3]([O:2][CH3:1])[C:14]([O:15][CH3:16])=[C:13]([O:17][CH3:18])[CH:12]=2)[CH2:5][CH2:6][N:7]=1

Participants

4

Procedure

A solution of the acetamide 43 (280 mg, 1.1 mmol) in toluene (5 mL) containing POCl3 (0.8 mL, 8.5 mmol) was heated at reflux under Ar for 2 h. The excess POCl3 and the solvent were evaporated under vacuum. The black residue was washed with petroleum ether (10 mL). The residue was dissolved in distilled water (10 mL) and made basic by 5% NH4OH aq (10 mL). The aqueous solution was extracted with CHCl3 (20, 10, and 5 mL). The combined CHCl3 layer was washed successively with water (10 mL) and saturated NaCl solution (10 mL) and dried over anhydrous Na2SO4. Evaporation of the filtrate and chromatography (ether:ethanol, 98:2 by volume, silica gel 230-400 mesh) gave compound 44 as a pale brown oil (230 mg, 89.2%): 1H NMR (CDCl3, 200 MHz) δ6.84 (s, 1H), 3.92 (s, 3H), 3.89 (s, 3H), 3.85 (s, 3H), 3.61 (t, 2H, J=8 Hz), 2.64 (t, 2H, J=8 Hz), 2.36 (s, 3H). EIMS m/e 235 (M+, 84).

Workup

  1. temperaturewas heated
  2. temperatureat reflux under Ar for 2 h
  3. customThe excess POCl3 and the solvent were evaporated under vacuum
  4. washThe black residue was washed with petroleum ether (10 mL)
  5. dissolutionThe residue was dissolved in distilled water (10 mL)
  6. extractionThe aqueous solution was extracted with CHCl3 (20, 10, and 5 mL)
  7. washThe combined CHCl3 layer was washed successively with water (10 mL) and saturated NaCl solution (10 mL)
  8. dry with materialdried over anhydrous Na2SO4
  9. customEvaporation of the filtrate and chromatography (ether:ethanol, 98:2 by volume, silica gel 230-400 mesh)

Sources & evidence

ORD record
ord-f7be6a220f8b439abe08047c1c9afe3a
Source dataset
uspto-grants-1995_07
Patent number
US05430062

Reaction notes

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