GB1090899A - Process for the preparation of phenazine derivatives - Google Patents
Process for the preparation of phenazine derivativesInfo
- Publication number
- GB1090899A GB1090899A GB3837866A GB3837866A GB1090899A GB 1090899 A GB1090899 A GB 1090899A GB 3837866 A GB3837866 A GB 3837866A GB 3837866 A GB3837866 A GB 3837866A GB 1090899 A GB1090899 A GB 1090899A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- phenazine
- aryl
- inorganic base
- organic
- 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
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/46—Phenazines
Abstract
Phenazine derivatives of the formula <FORM:1090899/C2/1> where R represents a halogen atom or an alkyl, aryl, aralkyl, alkaryl, alkoxy, thioalkyl, alkyl sulphonyl, aryl sulphonyl, hydroxy, amino or substituted amino group, m and n each represent 0, 1, 2, 3 or 4, the groups R being the same or different when m + n is greater than 1, may be obtained by reducing a 2,21-dinitrodiphenylamine of the formula <FORM:1090899/C2/2> with hydrazine in an alkaline medium. The reaction is suitably effected at a temperature above 20 DEG C. in the presence of a catalyst of activated charcoal or a metal of Group IB IIB or VIII of the Periodic Table and the alkaline medium may be provided by an alcoholic solution of an organic or inorganic base, but other solvents, e.g. dimethylformamide, ethanediol or t-butanol may also be used. The inorganic base may be an alkali or alkaline earth metal oxide or hydroxide and the organic base may be potassium tert.-butoxide. In an example 2-chloro-phenazine is prepared and some 2-ethoxyphenazine is also obtained.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3837866A GB1090899A (en) | 1966-08-26 | 1966-08-26 | Process for the preparation of phenazine derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3837866A GB1090899A (en) | 1966-08-26 | 1966-08-26 | Process for the preparation of phenazine derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1090899A true GB1090899A (en) | 1967-11-15 |
Family
ID=10403097
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3837866A Expired GB1090899A (en) | 1966-08-26 | 1966-08-26 | Process for the preparation of phenazine derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1090899A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3520888A (en) * | 1965-10-22 | 1970-07-21 | Pfizer & Co C | 3,4-dihydrophenazine-5,10-dioxides |
US3530130A (en) * | 1967-09-14 | 1970-09-22 | Hoffmann La Roche | 1-acylated-6-methoxyphenazine 5,10-dioxides |
-
1966
- 1966-08-26 GB GB3837866A patent/GB1090899A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3520888A (en) * | 1965-10-22 | 1970-07-21 | Pfizer & Co C | 3,4-dihydrophenazine-5,10-dioxides |
US3530130A (en) * | 1967-09-14 | 1970-09-22 | Hoffmann La Roche | 1-acylated-6-methoxyphenazine 5,10-dioxides |
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