Triethylamine → 6-methoxyisoquinolin-1(2H)-one

HRID 719837Notes

Reaction equation

HRID 719837 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[CH:6]=[CH:7]C(O)=O.C([N:16]([CH2:19]C)CC)C.ClC(OCC)=[O:23].[N-]=[N+]=[N-].[Na+]>CC(C)=O.O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:11](=[CH:12][CH:13]=1)[C:19](=[O:23])[NH:16][CH:7]=[CH:6]2

Participants

7

Conditions

Temperature
210 °C

Procedure

To a solution of 3-methoxy cinnamic acid (11.04 g, 62 mmol), triethylamine (12.52 g, 124 mmol) in acetone (80 mL) was added ethyl chloroformate dropwise at 0° C. After stirring at this temperature for 1 h, aqueous NaN3 (6.40 g, 100 mmol in 35 mL H2O) was added dropwise and the reaction mixture was stirred for 16 h at the ambient temperature. Water (100 mL) was added to the mixture and the volatile was removed in vacuo. The resulting slurry was extracted with toluene (3×50 mL) and the combined organic layers were dried over MgSO4. This dried solution was added dropwise to a heated solution of diphenylmethane (50 mL) and tributylamine (30 mL) at 190° C. The toluene was distilled off as added. After complete addition, the reaction temperature was raised to 210° C. for 2 h. After cooling, the precipitated product was collected by filtration, washed with hexane (2×50 mL), dried to yield a white solid (5.53 g, 51%), MS m/z 176 (M++H).

Workup

  1. stirringthe reaction mixture was stirred for 16 h at the ambient temperature
  2. customthe volatile was removed in vacuo
  3. extractionThe resulting slurry was extracted with toluene (3×50 mL)
  4. dry with materialthe combined organic layers were dried over MgSO4
  5. additionThis dried solution was added dropwise to a heated solution of diphenylmethane (50 mL) and tributylamine (30 mL) at 190° C
  6. distillationThe toluene was distilled off
  7. additionas added
  8. additionAfter complete addition
  9. temperatureAfter cooling
  10. filtrationthe precipitated product was collected by filtration
  11. washwashed with hexane (2×50 mL)
  12. customdried

Sources & evidence

ORD record
ord-46a368169eff4d7ba1c851f1474a7b4a
Source dataset
uspto-grants-2006_11
Patent number
US07132504B2

Reaction notes

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