GB1024907A - Quinazolines - Google Patents
QuinazolinesInfo
- Publication number
- GB1024907A GB1024907A GB4156963A GB4156963A GB1024907A GB 1024907 A GB1024907 A GB 1024907A GB 4156963 A GB4156963 A GB 4156963A GB 4156963 A GB4156963 A GB 4156963A GB 1024907 A GB1024907 A GB 1024907A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- hydrogen
- alkoxy
- chlorine
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
Abstract
The invention comprises 2-guanidinoquinazolines of the formula <FORM:1024907/C2/1> wherein R1, R2, R3 and R4 each represent hydrogen, chlorine, bromine, alkyl, alkoxy, alkenyloxy or aralkoxy, provided that not more than three of R1 to R4 are hydrogen atoms, provided that where one of R1 to R4 is chlorine at least one other of R1 to R4 is selected from the specified groups other than hydrogen, and provided that where one of R1 to R4 is an alkyl or alkoxy group at least one other of R1 to R4 is selected from the specified atoms or groups other than hydrogen, alkyl and alkoxy; R5 represents hydrogen or alkyl; and R6 represents hydrogen, alkyl, aralkyl or an aromatic group (e.g. phenyl or chlorophenyl); and acid addition and quaternary salts of such compounds. The above guanidinoquinazolines are prepared by reacting 1,2-dihydroquinoline of the formula <FORM:1024907/C2/2> (wherein each R represents an alkyl group and X- is the anion of the acid HX) with a dicyandiamide of the formula <FORM:1024907/C2/3> in the presence of an acid capable of forming an acid addition salt with the 1,2-dihydroquinoline.ALSO:A bacteriostatic composition comprises a 2-guanidino-quinazoline of the formula:- <FORM:1024907/A5-A6/1> wherein R1, R2, R3 and R4 each represent hydrogen, chlorine, bromine, alkyl, alkoxy, alkenyloxy or aralkoxy, provided that not more than three of R1 to R4 are hydrogen atoms, provided that where one or R1 to R4 is chlorine at least one other of R1 to R4 is selected from the specified groups other than hydrogen, and provided that where one of R1 to R4 is an alkyl or alkoxy group at least one other of R1 to R4 is selected from the specified atoms or groups other than hydrogen, alkyl and alkoxy; R5 represents hydrogen or alkyl; and R6 represents hydrogen, alkyl, aralkyl or an aromatic group (e.g. phenyl or chlorophenyl); or an acid addition or quaternary salt thereof in admixture with a diluent such as water, soap, a sodium salt of a long-chain alkylated aromatic sulphonic acid, toluene, cyclohexane, petroleum ether, chloroform, chlorobenzene, castor oil, sperm oil, cottonseed oil, rape oil, mineral oil or talc, and formulated into solutions, suspensions, emulsions, dispersions, lotions, pastes, creams, ointments or powders. The above compositions or the active ingredients thereof per se may be used to protect cloth, leather, plants, vegetables and fruit against bacteria and fungi.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4156963A GB1024907A (en) | 1963-10-22 | 1963-10-22 | Quinazolines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4156963A GB1024907A (en) | 1963-10-22 | 1963-10-22 | Quinazolines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1024907A true GB1024907A (en) | 1966-04-06 |
Family
ID=10420305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4156963A Expired GB1024907A (en) | 1963-10-22 | 1963-10-22 | Quinazolines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1024907A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003026667A1 (en) * | 2001-09-24 | 2003-04-03 | Synaptic Pharmaceutical Corporation | Quinazolino- and quinolino- guanidines as ligands for the neurop eptide ff (npff) receptors |
-
1963
- 1963-10-22 GB GB4156963A patent/GB1024907A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003026667A1 (en) * | 2001-09-24 | 2003-04-03 | Synaptic Pharmaceutical Corporation | Quinazolino- and quinolino- guanidines as ligands for the neurop eptide ff (npff) receptors |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1024917A (en) | Pyridazones and compositions containing them for influencing plant growth | |
GB1071478A (en) | Dinitroaniline derivatives and herbicidal compositions containing them | |
GB1083377A (en) | Esters of thiophosphorus acids | |
GB1084134A (en) | Novel quaternary ammonium salts, their preparation and use as surface-active agents | |
US2470077A (en) | Phenylethyl sulfones | |
GB1024907A (en) | Quinazolines | |
GB1048814A (en) | Process for reducing the toxicity of and extending the active period of organic phosphorus compounds | |
US2847473A (en) | 2, 3-dichloro-nu-(omicron-chlorobenzylidene) aniline | |
US2569408A (en) | Quaternary salts-alkylbenzyl alkyl dimethyl ammonium halides | |
GB1388394A (en) | Substituted cinnamanilides and biocidal uses thereof | |
DE1050768B (en) | Process for the preparation of phenylthionophosphonic acid esters | |
GB1018805A (en) | Organotin compound | |
US3835184A (en) | Formamide derivatives | |
US3223711A (en) | Cyclic imide addition products | |
GB1113370A (en) | N-substituted phthalimides | |
US3300377A (en) | Biocidal quaternary ammonium aromatic cyclic imides | |
GB900779A (en) | Quinazolines | |
US3004885A (en) | Salts of alkanethiols | |
US3657318A (en) | Aryl mercapto-carboxylic acid phenyl esters | |
GB1043042A (en) | Improvements in or relating to microbiocidal compositions | |
AT288780B (en) | Pesticides | |
US3716587A (en) | N-(phenyl or benzyl)-n,n'-bis-(1-amino-2,2,2-trichloro)-ethyl)alkyleniamines | |
US3702344A (en) | Novel formamide derivatives | |
GB1009200A (en) | Trifluoromethylanilide derivatives | |
GB1094882A (en) | Phenylamine ammonium salts |