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ES345681A1 - Substituted tetraazaphenalenes and their salts, a process for their production and compositions containing them - Google Patents

Substituted tetraazaphenalenes and their salts, a process for their production and compositions containing them

Info

Publication number
ES345681A1
ES345681A1 ES345681A ES345681A ES345681A1 ES 345681 A1 ES345681 A1 ES 345681A1 ES 345681 A ES345681 A ES 345681A ES 345681 A ES345681 A ES 345681A ES 345681 A1 ES345681 A1 ES 345681A1
Authority
ES
Spain
Prior art keywords
phenyl
compounds
hydrazine
group
general formula
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
ES345681A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
JR Geigy AG
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 JR Geigy AG filed Critical JR Geigy AG
Publication of ES345681A1 publication Critical patent/ES345681A1/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07D487/06Peri-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Compounds of the general formula and acid addition and quaternary ammonium salts thereof wherein R 1 represents the hyrazzino or phenylhydrazino radical or an amino radical corresponding to the Formula II: wherein R 5 represents hydrogen, a low alkyl group, a mononuclear aryl or aralkyl radical the aromatic nuclei of which can be substituted by halogen up to the atomic number 35, low alkyl, low alkoxy and trifluoromethyl, or R 5 and R 6 together with the adjacent nitrogen atom, represent a heterocyclic radical having 5 to 7 ring members and containing 4 to 6 carbon atoms, which radical also can contain oxygen or another nitrogen function in its ring, and can contain a fused, mononuclear aromatic carbocyclic ring optionally substituted by halogen up to the atomic number 35, low alkyl, low alkoxy or trifluoromethyl, and R 6 has the meaning of R 5 with the exception of hydrogen, R 2 represents hydrogen, a low alkyl group, the phenyl group or the benzyl group, R 3 represents hydrogen or the phenyl group, and R 4 represents hydrogen, halogen up to the atomic number 35, a low alkyl or alkoxy group, the hydroxy group or carboxyl group are prepared by reacting the compound of the general Formula III: wherein Y represents a chlorine or bromine atom or the mercapto group with a hydrazine, phenyl hydrazine or an amine of the formula HNR 5 R 6 in the presence of an acid binding agent and optionally with the formation of the desired salt except that when Y is mercapto and R 2 , R 3 and R 4 simultaneously are H, or when R 2 is phenyl and Y is halogen and R 3 and R 4 are H, hydrazine is not used. Compounds wherein R 1 is a group of Formula II above are novel. Compounds of the above general Formula III wherein Y represents the mercapto group are prepared by reacting a compound of the general Formula V with, for example, phosphorus pentasulphide. Compounds of the above Formula III wherein Y represents halogen may be prepared by reaction of the ketone of the last formula above with a phosphorus halide or oxyhalide, or by reaction of a halogen in the presence of an alkali metal salt of acetic acid with a compound of the general formula Compounds of the general Formula V wherein R 2 and R 3 represent hydrogen, can be produced e.g. from a 3-(alpha, alpha-dibromomethyl)- phthalic acid anhydride substituted according to the definition of R 4 , by reaction with at least double the molar amount of hydrazine or hydrazine hydrate. On treating these compounds with alkylating agents such as alkyl or benzyl halides in the presence of a base, compounds of the general Formula V are obtained therefrom wherein R 2 is a low alkyl group or the benzyl group and R 3 is hydrogen. 3-(Alpha, alpha - dibromomethyl) - phthalic acid anhydride can be obtained by brominating 3-methyl phthalic acid anhydride compounds substituted corresponding to the definition of R 4 can be obtained analogously. Compounds of the general Formula V wherein R 2 is phenyl and R 3 is hydrogen can be obtained, e.g. from the 3-(alpha, alpha-dibromomethyl)- phthalic acid anhydrides mentioned above by first hydrolysing these, then reacting the 7 - carboxy - 3 - hydroxy - phthalides formed with phenyl hydrazine to form the 8-carbozy-2- phenyl-1(2H)-phthalazinones, esterifying these and reacting the 8-carbalkoxy-2-phenyl-1(2H)- phthalazinones with hydrazine to form the compounds of general Formula V wherein R 2 is phenyl and R 3 is hydrogen. Compounds of general Formula V wherein R 3 is phenyl and R 4 is hydrogen can be obtained by reacting an ester of 8-carboxy-4-phenyl-1(2H)- phthalazinone with hydrazine. Thus, for example, 8 - carboxy - 4 - phenyl - 1(2H) - phthalazinone, M.P. 257-259 C., is obtained from the known 3-benzoyl phthalic acid and hydrazine. On using an alkyl or phenyl hydrazine, 8 - carboxy - 4 - phenyl - 1(2H) - phthalazinones correspondingly substituted in the 2-position can be obtained in an analogous way. Esters of 8 - carbalkoxy - 4 - phenyl - 1(2H) - phthalazinones, e.g. the methyl or ethyl ester, are obtained by esterifying the 8-carboxy-4-phenyl-1(2H)- phthalazinones. "Low" as used above indicates groups containing up to 4 carbon atoms.
ES345681A 1966-10-03 1967-10-02 Substituted tetraazaphenalenes and their salts, a process for their production and compositions containing them Expired ES345681A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US58398066A 1966-10-03 1966-10-03

Publications (1)

Publication Number Publication Date
ES345681A1 true ES345681A1 (en) 1968-11-16

Family

ID=24335405

Family Applications (2)

Application Number Title Priority Date Filing Date
ES345680A Expired ES345680A1 (en) 1966-10-03 1967-10-02 Substituted tetraazaphenalenes and their salts, a process for their production and compositions containing them
ES345681A Expired ES345681A1 (en) 1966-10-03 1967-10-02 Substituted tetraazaphenalenes and their salts, a process for their production and compositions containing them

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ES345680A Expired ES345680A1 (en) 1966-10-03 1967-10-02 Substituted tetraazaphenalenes and their salts, a process for their production and compositions containing them

Country Status (14)

Country Link
AT (3) AT276411B (en)
BE (2) BE704584A (en)
CH (2) CH515909A (en)
DE (2) DE1695039A1 (en)
DK (2) DK123653B (en)
ES (2) ES345680A1 (en)
FI (2) FI47770C (en)
FR (3) FR1550404A (en)
GB (2) GB1208114A (en)
GR (2) GR37757B (en)
IL (2) IL28709A (en)
NL (2) NL6713378A (en)
NO (1) NO122482B (en)
SE (2) SE335346B (en)

Also Published As

Publication number Publication date
DK123653B (en) 1972-07-17
IL28709A (en) 1973-01-30
GR37757B (en) 1969-07-11
ES345680A1 (en) 1968-11-16
FI47769C (en) 1974-03-11
CH515909A (en) 1971-11-30
FR7211M (en) 1969-08-25
SE335346B (en) 1971-05-24
SE329401B (en) 1970-10-12
FI47769B (en) 1973-11-30
GR37758B (en) 1969-07-11
FR7210M (en) 1969-08-25
NL6713374A (en) 1968-04-04
FI47770C (en) 1974-03-11
BE704584A (en) 1968-04-02
FR1550404A (en) 1968-12-20
FI47770B (en) 1973-11-30
NL6713378A (en) 1968-04-04
GB1208114A (en) 1970-10-07
NO122482B (en) 1971-07-05
BE704585A (en) 1968-04-02
AT273980B (en) 1969-09-10
DE1695039A1 (en) 1971-04-08
CH486477A (en) 1970-02-28
DK120755B (en) 1971-07-12
GB1204522A (en) 1970-09-09
AT276411B (en) 1969-11-25
DE1695038A1 (en) 1971-04-08
AT273981B (en) 1969-09-10
IL28710A (en) 1973-01-30

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