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 themInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/06—Peri-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.
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) |
-
1967
- 1967-09-30 CH CH1363967A patent/CH515909A/en not_active IP Right Cessation
- 1967-09-30 CH CH1364067A patent/CH486477A/en not_active IP Right Cessation
- 1967-10-02 FI FI263267A patent/FI47770C/en active
- 1967-10-02 SE SE1346167A patent/SE335346B/xx unknown
- 1967-10-02 NO NO16994967A patent/NO122482B/no unknown
- 1967-10-02 BE BE704584D patent/BE704584A/xx unknown
- 1967-10-02 DE DE19671695039 patent/DE1695039A1/en active Pending
- 1967-10-02 IL IL2870967A patent/IL28709A/en unknown
- 1967-10-02 DK DK487867A patent/DK123653B/en unknown
- 1967-10-02 FR FR1550404D patent/FR1550404A/fr not_active Expired
- 1967-10-02 DE DE19671695038 patent/DE1695038A1/en active Pending
- 1967-10-02 BE BE704585D patent/BE704585A/xx unknown
- 1967-10-02 GB GB4467967A patent/GB1208114A/en not_active Expired
- 1967-10-02 NL NL6713378A patent/NL6713378A/xx unknown
- 1967-10-02 NL NL6713374A patent/NL6713374A/xx unknown
- 1967-10-02 DK DK487767A patent/DK120755B/en unknown
- 1967-10-02 FI FI263167A patent/FI47769C/en active
- 1967-10-02 GR GR670137757A patent/GR37757B/en unknown
- 1967-10-02 AT AT880368A patent/AT276411B/en active
- 1967-10-02 ES ES345680A patent/ES345680A1/en not_active Expired
- 1967-10-02 GR GR670137758A patent/GR37758B/en unknown
- 1967-10-02 IL IL2871067A patent/IL28710A/en unknown
- 1967-10-02 AT AT891667A patent/AT273981B/en active
- 1967-10-02 SE SE1346067A patent/SE329401B/xx unknown
- 1967-10-02 AT AT891467A patent/AT273980B/en active
- 1967-10-02 GB GB44680/67A patent/GB1204522A/en not_active Expired
- 1967-10-02 ES ES345681A patent/ES345681A1/en not_active Expired
- 1967-12-29 FR FR134301A patent/FR7211M/fr not_active Expired
- 1967-12-29 FR FR134300A patent/FR7210M/fr not_active Expired
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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