GB1024907A - Quinazolines - Google Patents

Quinazolines

Info

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
Application number
GB4156963A
Inventor
Joseph Patrick Brown
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.)
Monsanto Chemicals Ltd
Original Assignee
Monsanto Chemicals Ltd
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 Monsanto Chemicals Ltd filed Critical Monsanto Chemicals Ltd
Priority to GB4156963A priority Critical patent/GB1024907A/en
Publication of GB1024907A publication Critical patent/GB1024907A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/78Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
    • C07D239/84Nitrogen 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.
GB4156963A 1963-10-22 1963-10-22 Quinazolines Expired GB1024907A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (1)

* Cited by examiner, † Cited by third party
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

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