SE8204765L - 2- (O-CARBOXYPHENYLAMINO) -6H-PYRIMIDO (2, 1-B) -CHINAZOLONE-6 AND THEIR DERIVATIVES THEREOF, THEIR PREPARATION AND COMPOSITIONS CONTAINING ITS - Google Patents

2- (O-CARBOXYPHENYLAMINO) -6H-PYRIMIDO (2, 1-B) -CHINAZOLONE-6 AND THEIR DERIVATIVES THEREOF, THEIR PREPARATION AND COMPOSITIONS CONTAINING ITS

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Publication number
SE8204765L
SE8204765L SE8204765A SE8204765A SE8204765L SE 8204765 L SE8204765 L SE 8204765L SE 8204765 A SE8204765 A SE 8204765A SE 8204765 A SE8204765 A SE 8204765A SE 8204765 L SE8204765 L SE 8204765L
Authority
SE
Sweden
Prior art keywords
formula
image
carbon atoms
compound
alkyl
Prior art date
Application number
SE8204765A
Other languages
Swedish (sv)
Other versions
SE440908B (en
SE8204765D0 (en
Inventor
V A Portnyagina
V K Karp
I S Barkova
F P Trinus
N A Mokhort
A G Fadeicheva
G I Kozhushko
T K Ryabukha
A G Panteleimonov
V V Kljushin
J N Dobrovolsky
L M Kirichek
A A Medvedovsky
G A Getman
J D Usenko
V M Sidelnikov
N F Danilevsky
Y P Solsky
Original Assignee
Ki Nii Farmakologii I
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ki Nii Farmakologii I filed Critical Ki Nii Farmakologii I
Priority to SE8204765A priority Critical patent/SE440908B/en
Publication of SE8204765D0 publication Critical patent/SE8204765D0/en
Publication of SE8204765L publication Critical patent/SE8204765L/en
Publication of SE440908B publication Critical patent/SE440908B/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Pharmaceutically usable 2-(o-carboxyphenylamino)-6H-pyrimido(2,1-b)quinazoline 6 with the formula<IMAGE>Further derivative of this compound with the formula<IMAGE>where A+ is an alkaline metal, monoethanolamine or diethylamine.IN addition a derivative of the stated compound with the formula<IMAGE>where R represents OH or alkyloxide with 1-4 carbon atoms or NHR2, where R1 represents H, alkyl with 1-4 carbon atoms or phenyl as well as alkyl and A are salts of inorganic acids.The final derivative of the given compound with the formula<IMAGE>where R represents alkyloxide with 1-4 carbon atoms or R1 represents alkyl with 1-4 carbon atoms.Furthermore, a process for producing the given formula comprising in that 2.4 dichloropyrimidine is converted with a sodium salt of anthranilic acid or subtitesters or amides of anthranilic acid in a hydrous or an organic solution at 90-120 degrees C for several hours.Furthermore, this refers to a hemotherapeutic composition, in which the component contains the above given compound or that and a pharmaceutically approved carrier material.
SE8204765A 1982-08-19 1982-08-19 2-(o-carboxyphenylamino)-6H-pyrimido(2,1-b)quinazoline and derivative thereof and compositions thereof SE440908B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SE8204765A SE440908B (en) 1982-08-19 1982-08-19 2-(o-carboxyphenylamino)-6H-pyrimido(2,1-b)quinazoline and derivative thereof and compositions thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE8204765A SE440908B (en) 1982-08-19 1982-08-19 2-(o-carboxyphenylamino)-6H-pyrimido(2,1-b)quinazoline and derivative thereof and compositions thereof

Publications (3)

Publication Number Publication Date
SE8204765D0 SE8204765D0 (en) 1982-08-19
SE8204765L true SE8204765L (en) 1984-02-20
SE440908B SE440908B (en) 1985-08-26

Family

ID=20347568

Family Applications (1)

Application Number Title Priority Date Filing Date
SE8204765A SE440908B (en) 1982-08-19 1982-08-19 2-(o-carboxyphenylamino)-6H-pyrimido(2,1-b)quinazoline and derivative thereof and compositions thereof

Country Status (1)

Country Link
SE (1) SE440908B (en)

Also Published As

Publication number Publication date
SE440908B (en) 1985-08-26
SE8204765D0 (en) 1982-08-19

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