4-Hydroxybenzaldehyde → HCID 178487364, compound

HRID 253212Notes

Reaction equation

HRID 253212 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]([C:12](=O)[CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:10]#[N:11])[CH:6]=[CH:7][CH:8]=1.[NH2:21][NH2:22].[OH:23][C:24]1[CH:31]=[CH:30][C:27]([CH:28]=O)=[CH:26][CH:25]=1.[F:32][C:33]([F:38])([F:37])[C:34]([OH:36])=[O:35]>C(O)C>[F:32][C:33]([F:38])([F:37])[C:34]([OH:36])=[O:35].[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C:28]([C:27]3[CH:30]=[CH:31][C:24]([OH:23])=[CH:25][CH:26]=3)=[N:11][C:10]3[NH:21][N:22]=[C:12]([CH2:13][C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=4)[C:9]=3[C:5]=2[CH:4]=1

Participants

6

Reactant 4

HCID 1264-HydroxybenzaldehydeHCID 6422Trifluoroacetic acidHCID 9321HydrazineHCID 59627809HCID 59627809, compound

Product 1

HCID 178487364HCID 178487364, compoundYield 34%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
70 °C

Procedure

2-[3-(methyloxy)phenyl]-3-oxo-4-phenylbutanenitrile (100 mg, 0.38 mmol) was dissolved in ethanol (1 mL), and anhydrous hydrazine (98%, 14 μL, 0.45 mmol) was added. The resulting mixture was heated at reflux for 1 hour. It was cooled, concentrated, and the residue was dried under vacuum for one hour. To this residue was added of 4-hydroxybenzaldehyde (69 mg, 0.57 mmol) and trifluoroacetic acid (1 mL), and the mixture was heated at 70° C. for 18 hours. Then the reaction mixture was concentrated, dissolved in 10 mL of N,N-dimethylformamide and purified by preparatory reverse phase HPLC (Shimadzu LC-8A HPLC, Waters Xterra C18 30 mm×100 mm column, acetonitrile-water-trifluoroacetic eluent). After concentration then lyophillization of the pure fractions 4-[8-(methyloxy)-1-(phenylmethyl)-3H-pyrazolo[3,4-c]isoquinolin-5-yl]phenol trifluoroacetic acid salt (63 mg, 0.13 mmol, 34% yield) was obtained. 1H NMR (400 MHz, d6-DMSO): 7.97-7.94 (d, 1H), 7.50-7.48 (d, 2H), 7.30-7.25 (m, 6H), 7.06-7.02 (m, 1H), 6.95-6.93 (d, 2H), 4.60 (s, 2H), 3.76 (s, 3H); MS (EI) for C24H19N3O2: 382 (MH+).

Workup

  1. temperatureThe resulting mixture was heated
  2. temperatureat reflux for 1 hour
  3. temperatureIt was cooled
  4. concentrationconcentrated
  5. customthe residue was dried under vacuum for one hour
  6. concentrationThen the reaction mixture was concentrated
  7. dissolutiondissolved in 10 mL of N,N-dimethylformamide
  8. custompurified by preparatory reverse phase HPLC (Shimadzu LC-8A HPLC, Waters Xterra C18 30 mm×100 mm column, acetonitrile-water-trifluoroacetic eluent)
  9. concentrationAfter concentration

Sources & evidence

ORD record
ord-1f87e1381b6a47e3b0fb1ce774dc46f9
Source dataset
uspto-grants-2011_01
Patent number
US07872014B2

Reaction notes

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