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  • Articles: DFG German National Licenses  (2)
  • 1995-1999  (1)
  • 1990-1994  (1)
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  • Articles: DFG German National Licenses  (2)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1237-1241 
    ISSN: 0009-2940
    Keywords: Quinolin-2(1H)-ones ; 4-amino-3-pyridinio- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4-Amino-3-pyridinioquinolin-2(1H)-one Chlorides and 3,4-Diaminoquinolin-2(1H)-onesN;-(Chloroacetyl)anthranilonitriles 1 react with the pyridines 2 to form the 4-amino-3-pyridinioquinolin-2(1H)-one chlorides 4, which are converted into the pyrido[1',2′ : 1,2]imidazo[5,4-c]- quinolin-6(5H)-ones 6 in the presence of sodium hydroxide or by cyclooxidation with bromine. Treatment of 4 with hydrazine hydrate yields the 3,4-diaminoquinolin-2(1H)-ones 9. Analogously to other o-diamines the substituted imidazo [4,5-c]- quinolinones 12, the pyrazino[2,3-c]quinolinones 13, 14, the 1,2,5-thiadiazolo[3,4-c]quinolin-4-one 15a and the 1,2,5-selena-diazolo[3,4-c]quinolin-4-one 15b are obtainable from 9a. With chloroacetyl chloride 9a provides the oxazino[2,3-b]quinolin-2-one 11.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1995 (1995), S. 787-791 
    ISSN: 0947-3440
    Keywords: Pyridines ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-[(Chloroacetyl)amino]acrylonitriles 1 and 3-[(chloroacetyl)-amino]propionitriles 4 were allowed to react with pyridine to form the 1-(4-amino-3-pyridyl)pyridinium salts 3 and 1-(4-amino-5,6-dihydro-3-pyridyl)pyridinium salts 6. Dehydrogenation of 6 with bromine in glacial acetic acid afforded 1-(4-amino-3-pyridyl)pyridinium bromides 7. Treatment of 3 and 7 with hydrazine hydrate yielded the 3,4-diamino-2(1H)-pyridinones 8. Analogously to other ortho-diamines, the substituted [1,2,5]thiadiazolo[3,4-c]pyridin-4-one 10, [1,2,5]selenadiazolo[3,4-c]pyridin-4-one 11, and further derivatives were obtained from 8. N-(Chloroacetyl) derivatives of acetylacetoneimide 13 and 3-oxo-3-phenyl-2-(phenylhydrazono)propionamide 17 were treated with pyridine to give 1-(3-pyridyl)-pyridinium salts 14 and 18, respectively.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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