GB738013A - New nitrogen containing heterocyclic compounds - Google Patents
New nitrogen containing heterocyclic compoundsInfo
- Publication number
- GB738013A GB738013A GB2587852A GB2587852A GB738013A GB 738013 A GB738013 A GB 738013A GB 2587852 A GB2587852 A GB 2587852A GB 2587852 A GB2587852 A GB 2587852A GB 738013 A GB738013 A GB 738013A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- diphenylamine
- nitro
- dibromo
- benzoylamino
- 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
Landscapes
- Photoreceptors In Electrophotography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises compounds of the formula <FORM:0738013/IV (b)/1> and their production from 2-acylamino-diphenylamines of the formula <FORM:0738013/IV (b)/2> by heating with a phosphorus oxide, halide or oxyhalide; R is hydrogen or an alkyl, aryl, aralkyl or heterocyclic radical, R1 is alkyl, aryl or aralkyl and R2 is hydrogen, lower alkyl or aralkyl; and nuclei X and Y may carry substituents which are not affected by the reaction conditions, e.g. alkylsulphonyl, halogen, nitro or alkoxy. The reaction may be carried out in an inert solvent such as nitrobenzene, but this is unnecessary if R2 is hydrogen. Examples show the production of the following substituted 2 : 3 : 6 : 7 - dibenz - 1 : 4 - diazepines (the nature of the Group R2 in the starting material being indicated):-1 - methyl - 31 - nitro - 5 - phenyl (R2=methyl), 1 - methyl - 31 - nitro - 5 - p - nitrophenyl (R2=methyl), 1 - methyl - 211 : 31 - dinitro - 5 - phenyl (R2=H and methyl), 211 : 31-dibromo - 1 - methyl - 5 - phenyl (R2=H and methyl), 211 - methoxy - 1 - methyl - 31 - nitro - 5 - phenyl (R2=H), 211 - methoxy - 1 : 5 - dimethyl-31-nitro (R2=H, acylamino compound prepared in situ), 211-methoxy-1-methyl-31-nitro (R2=H, acylamino compound prepared in situ), 1 - methyl - 5 - phenyl (R2=H), and 1 : 5-diphenyl (R2=H). Diphenylamines.-The following are made by direct acylation:- 2-benzoylamino-N-methyldiphenylamine, 2 - benzoylamino - 4 : 41 - dibromo-diphenylamine, 2-benzoylamino-4 : 41-dibromo - N - methyl - diphenylamine, 2 - benzoylamino - 41 - methoxy - N - methyl - 4 - nitro - diphenylamine, 4 - nitro - 2 - (p - nitrobenzoylamino) - diphenylamine, 2 - benzoylamino - 4 : 41 - dinitro - diphenylamine, 2 - benzoylamino - 4 : 41 - dinitro - N - methyl - diphenylamine and 2 - benzoylamino - triphenylamine. The following are made by N-methylation:-N - methyl - 2 - nitro - diphenylamine, 2 - amino - 41 - methoxy - N - methyl - 4 - nitro - diphenylamine, 2 - amino - 4 : 41 - dinitro - N - methyl - diphenylamine, 2 - benzomethylamino - 4 : 41 - dibromo - N - methyl - diphenylamine, 4 : 41 - dibromo - N - methyl - 2 - nitro - diphenylamine, 2 - benzomethylamino - N - methyl - 4 - nitro - diphenylamine, 2 - benzomethylamino - 4 : 41 - dinitro - N - methyl - diphenylamine and N - methyl - 4 - nitro - 2 - (p - nitrobenzomethylamino) - diphenylamine. The following are made by reduction of the corresponding nitro compounds:- 2 - amino - N - methyl - diphenylamine, 2 - amino - 4 : 41 - dinitro - diphenylamine, 2 - amino - 41 - methoxy-4 - nitro - diphenylamine, 2 - amino - 4 : 41 - dibromo - diphenylamine and 2 - amino - 4 : 41 - dibromo - N - methyl - diphenylamine. 4 : 41 - Dibromo - 2 - nitro - diphenylamine is made by condensing aniline with 2 : 5-dibromonitrobenzene and brominating the product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2587852A GB738013A (en) | 1952-10-15 | 1952-10-15 | New nitrogen containing heterocyclic compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2587852A GB738013A (en) | 1952-10-15 | 1952-10-15 | New nitrogen containing heterocyclic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB738013A true GB738013A (en) | 1955-10-05 |
Family
ID=10234836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2587852A Expired GB738013A (en) | 1952-10-15 | 1952-10-15 | New nitrogen containing heterocyclic compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB738013A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3129216A (en) * | 1964-04-14 | S-basic substituted-s-dibenso-fb | ||
DE1280879B (en) * | 1960-08-16 | 1968-10-24 | Wander Ag Dr A | 11-Basic substituted 5H-dibenzo [b, e] -1, 4-diazepines |
EP0076017A2 (en) * | 1981-09-24 | 1983-04-06 | A.H. Robins Company, Incorporated | Phenyl substituted pyrido(1,4)benzodiazepines and intermediates therefor |
CN112500395A (en) * | 2020-12-02 | 2021-03-16 | 吉林奥来德光电材料股份有限公司 | Dibenzo nitrogen-containing seven-membered heterocyclic organic compound, preparation method thereof and organic electroluminescent device |
CN112592355A (en) * | 2020-12-23 | 2021-04-02 | 吉林奥来德光电材料股份有限公司 | Organic phosphorus luminescent compound, preparation method thereof and organic electroluminescent device |
-
1952
- 1952-10-15 GB GB2587852A patent/GB738013A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3129216A (en) * | 1964-04-14 | S-basic substituted-s-dibenso-fb | ||
DE1280879B (en) * | 1960-08-16 | 1968-10-24 | Wander Ag Dr A | 11-Basic substituted 5H-dibenzo [b, e] -1, 4-diazepines |
EP0076017A2 (en) * | 1981-09-24 | 1983-04-06 | A.H. Robins Company, Incorporated | Phenyl substituted pyrido(1,4)benzodiazepines and intermediates therefor |
EP0076017B1 (en) * | 1981-09-24 | 1990-08-16 | A.H. Robins Company, Incorporated | Phenyl substituted pyrido(1,4)benzodiazepines and intermediates therefor |
CN112500395A (en) * | 2020-12-02 | 2021-03-16 | 吉林奥来德光电材料股份有限公司 | Dibenzo nitrogen-containing seven-membered heterocyclic organic compound, preparation method thereof and organic electroluminescent device |
CN112500395B (en) * | 2020-12-02 | 2022-03-08 | 吉林奥来德光电材料股份有限公司 | Dibenzo nitrogen-containing seven-membered heterocyclic organic compound, preparation method thereof and organic electroluminescent device |
CN112592355A (en) * | 2020-12-23 | 2021-04-02 | 吉林奥来德光电材料股份有限公司 | Organic phosphorus luminescent compound, preparation method thereof and organic electroluminescent device |
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