HCID 19030722, compound → HCID 19030970, compound

HRID 266779Notes

Reaction equation

HRID 266779 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH:14]=[CH:13][C:11]2=[O:12])=[CH:6][CH:5]=1)([O-])=O>C(O)(=O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([N:10]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH:14]=[CH:13][C:11]2=[O:12])=[CH:8][CH:9]=1

Participants

3

Procedure

To 10% Pd--C (0.1 g) is added acetic acid (20 ml) and then 1-(4-nitrophenyl)carbostyril (0.9 g) and the mixture is subjected to catalytic reduction at 80° C. under normal pressure. After completion of the reaction, 10% Pd--C is removed by filtration and the resulting solution is concentrated under reduced pressure. To the concentrate is added water and the solution is made alkaline with an aqueous sodium hydroxide solution and then extracted with dichloromethane. The extract is washed with water and dried over magnesium sulfate. The solvent is distilled off under reduced pressure and the residue is purified by silica gel column chromatography and recrystallized from ethanol to give 1-(4-aminophenyl)carbostyril (0.66 g) as brown powders, m.p. 225°-230° C.

Workup

  1. customis subjected to catalytic reduction at 80° C. under normal pressure
  2. customis removed by filtration
  3. concentrationthe resulting solution is concentrated under reduced pressure
  4. additionTo the concentrate is added water
  5. extractionextracted with dichloromethane
  6. washThe extract is washed with water
  7. dry with materialdried over magnesium sulfate
  8. distillationThe solvent is distilled off under reduced pressure
  9. customthe residue is purified by silica gel column chromatography
  10. customrecrystallized from ethanol

Sources & evidence

ORD record
ord-742db0c931b44adc9e222e6e6bfee08d
Source dataset
uspto-grants-1997_07
Patent number
US05652247

Reaction notes

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