GB865675A - Improvements relating to heterocyclic nitrogen compounds and their use - Google Patents

Improvements relating to heterocyclic nitrogen compounds and their use

Info

Publication number
GB865675A
GB865675A GB40048/57A GB4004857A GB865675A GB 865675 A GB865675 A GB 865675A GB 40048/57 A GB40048/57 A GB 40048/57A GB 4004857 A GB4004857 A GB 4004857A GB 865675 A GB865675 A GB 865675A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
radical
compounds
alkyl radical
hydrogen
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
GB40048/57A
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.)
Novartis AG
National Starch and Chemical Investment Holding Corp
Original Assignee
JR Geigy AG
National Starch and Chemical Investment Holding Corp
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 JR Geigy AG, National Starch and Chemical Investment Holding Corp filed Critical JR Geigy AG
Publication of GB865675A publication Critical patent/GB865675A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/44Nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/06Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D239/08Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
    • C07D239/12Nitrogen atoms not forming part of a nitro radical

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises compounds of the formula: <FORM:0865675/IV (b)/1> where A is a saturated hydrocarbon radical bound to the two nitrogen atoms by a , b - or a -q -carbon atoms, R1 is a lipophilic aliphatic radical (particularly a saturated alkyl radical having 10-14 carbon atoms) and R2 is hydrogen, an alkyl radical containing 1-5 carbon atoms, or a cyclohexyl radical. The group A may be aliphatic or cycloaliphatic. These compounds may be prepared by reacting a diamine of formula R1-NH-A-NH-R2 with a cyanogen halide, advantageously in an inert organic solvent and heating if necessary and liberating the base with alkali. Lists of suitable diamines are given. In a modification, a cyanogen halide is reacted with a compound NH2-A-NH-R, where R is hydrogen or one of R1 and R2, and the other group(s) introduced by alkylation. The compounds of the invention form salts with inorganic and organic acids. The diamine starting materials may be prepared by alkylation of the primary diamines. The compounds of the invention have biocidal activity (see Groups IV(c) and VI). Reference has been directed by the Comptroller to Specification 765,547.ALSO:Textiles, e.g. blankets and restaurant and hotel linen, may be disinfected and rendered antiseptic by treatment with compositions containing a compound of formula:- <FORM:0865675/IV(c)/1> where A is a saturated hydrocarbon radical bound at the two nitrogen atoms by a , b - or a , g -carbon atoms, R1 is a lipophilic aliphatic radical (particularly a saturated alkyl radical having 10-14 carbon atoms), and R2 is hydrogen, an alkyl radical containing 1-5 carbon atoms, or a cyclohexyl radical. The compositions may be based on organic solvents, or aqueous solutions of salts of the above compounds may be used. Reference has been directed by the Comptroller to Specification 765,547.ALSO:Biocidal compositions contain as active ingredient a compound of formula <FORM:0865675/VI/1> where A is a saturated hydrocarbon radical bound at the two nitrogen atoms by a ,b - or a ,g -carbon atoms, R1 is a lipophilic aliphatic radical (particularly a saturated alkyl radical having 10-14 carbon atoms), and R2 is hydrogen, an alkyl radical containing 1-5 carbon atoms, or a cyclohexyl radical. The compounds may be used in solution or dispersion, and the compositions may contain inert carriers or fillers, cleansers, ointment bases, creams and other fungicidal and bactericidal agents. They may be used in cosmetic preparations as ointments and creams. They have fungicidal or fungistatic, bactericidal and algaecidal activity. Reference has been directed by the Comptroller to Specification 765,547.
GB40048/57A 1956-12-28 1957-12-24 Improvements relating to heterocyclic nitrogen compounds and their use Expired GB865675A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH865675X 1956-12-28

Publications (1)

Publication Number Publication Date
GB865675A true GB865675A (en) 1961-04-19

Family

ID=4543614

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40048/57A Expired GB865675A (en) 1956-12-28 1957-12-24 Improvements relating to heterocyclic nitrogen compounds and their use

Country Status (1)

Country Link
GB (1) GB865675A (en)

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