Phosphorus oxychloride → 1-Chloro-6-methoxy-3-methylisoquinoline

HRID 1895870

Reaction equation

HRID 1895870 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=O)[NH:8][C:7]([CH3:14])=[CH:6]2.O=P(Cl)(Cl)[Cl:17]>>[Cl:17][C:9]1[C:10]2[C:5](=[CH:4][C:3]([O:2][CH3:1])=[CH:12][CH:11]=2)[CH:6]=[C:7]([CH3:14])[N:8]=1

Participants

3

Procedure

Isoquinoline-1-one 43 was dissolved in POCl3 (2.5 mL) and heated at reflux for 1 h. The excess POCl3 was removed in vacuo and the residue was dissolved in CHCl3. The resulting solution was washed with 1N aq. NaOH, water and saturated ag. NaCl. Evaporation of the solvent gave crude 44 which was used directly in the next step.

Workup

  1. temperatureheated
  2. temperatureat reflux for 1 h
  3. customThe excess POCl3 was removed in vacuo
  4. dissolutionthe residue was dissolved in CHCl3
  5. washThe resulting solution was washed with 1N aq. NaOH, water and saturated ag
  6. customEvaporation of the solvent
  7. customgave crude 44 which

Sources & evidence

ORD record
ord-834bf06d1b42452fa9412b9fc8ede38d
Source dataset
uspto-grants-2013_08
Patent number
US08518874B2

Linked notes

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