N,N-Dimethylaniline → 4-Chloro-6-methoxy-7-(4-pyridylmethoxy)quinazoline

HRID 279519Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 279519
O=P(Cl)(Cl)[Cl:3].[CH3:6][O:7][C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][C:17]=1[O:18][CH2:19][C:20]1[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=1)[N:14]=[CH:13][NH:12][C:11]2=O.CN(C)C1C=CC=CC=1>C1(C)C=CC=CC=1>[Cl:3][C:11]1[C:10]2[C:15](=[CH:16][C:17]([O:18][CH2:19][C:20]3[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=3)=[C:8]([O:7][CH3:6])[CH:9]=2)[N:14]=[CH:13][N:12]=1

Komponenten

5

Versuchsvorschrift

Phosphorus oxytrichloride (0.1 ml) was added to a mixture of 6-methoxy-7-(4-pyridylmethoxy)-3,4-dihydroquinazolin-4-one (81 mg, 0.29 mmol) and N,N-dimethylaniline (0.1 ml) in toluene (5 ml), and the mixture heated at reflux for 1 hour. The volatiles were removed by evaporation and the residue partitioned between methylene chloride and aqueous ammonia. The organic extract was separated, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by chromatography on silica eluting with ethyl acetate progressing through increasingly polar mixtures to methanol/methylene chloride (1/9) to give 4-chloro-6-methoxy-7-(4-pyridylmethoxy)quinazoline (40 mg, 41%).

Aufarbeitung

  1. temperaturethe mixture heated
  2. temperatureat reflux for 1 hour
  3. customThe volatiles were removed by evaporation
  4. customthe residue partitioned between methylene chloride and aqueous ammonia
  5. extractionThe organic extract
  6. customwas separated
  7. dry with materialdried (MgSO4)
  8. customthe solvent removed by evaporation
  9. customThe residue was purified by chromatography on silica eluting with ethyl acetate progressing
  10. temperaturethrough increasingly polar mixtures to methanol/methylene chloride (1/9)

Quellen und Nachweise

ORD-Eintrag
ord-53968453313c4e5e8683beb8dcd02ce7
Quelldatensatz
uspto-grants-2002_03
Patentnummer
US06362336B1

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