GB855389A - Fungicidal compositions and basically substituted thiazoles for use therein - Google Patents

Fungicidal compositions and basically substituted thiazoles for use therein

Info

Publication number
GB855389A
GB855389A GB10130/57A GB1013057A GB855389A GB 855389 A GB855389 A GB 855389A GB 10130/57 A GB10130/57 A GB 10130/57A GB 1013057 A GB1013057 A GB 1013057A GB 855389 A GB855389 A GB 855389A
Authority
GB
United Kingdom
Prior art keywords
substituted
alkyl
ethyl
dimethylamino
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
GB10130/57A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
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, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB855389A publication Critical patent/GB855389A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles 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 in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles 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 in position 2
    • C07D277/70Sulfur atoms
    • C07D277/74Sulfur atoms substituted by carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/84Naphthothiazoles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention comprises thiazoles of the formulae: <FORM:0855389/IV(b)/1> and <FORM:0855389/IV(b)/2> where X is O or S; Y is H, alkyl, alkoxy or chlorine; Z is alkyl, alkoxy or chlorine; n is 2-4; R3 and R4 are H, C1-C6 alkyl or together form a ring; one of R5 and R6 is H and the other is acyl, carbalkoxy, carboxamide or N- substituted carboxamide; and R7 and R8 are C1-C6 alkyl. The compounds are prepared by reacting an alkali metal salt of the appropriate 2-hydroxy- or 2-meroapto-thiazole with an amine Hal-(Cn H2n). NR3 R4 or Hal-CH2-CH2-NR7R8, which may b liberated in situ from a salt thereof. In examples X is S, Y is H, Z is methyl, ethoxy or chlorine, Cn H2n is ethylene, propylene or trimethylene, NR3 R4 is amino, dimethylamino, diethylamino, di-isopropylamino, dibutylamino, ethyl-isopropylamino, ethyl-t-butylamino or morpholino, R5 is carbethoxy R6, is H and NR7 R8 is dimethylamino. The Specification also describes the preparation in the same way of other thiazoles having the general formula: <FORM:0855389/IV(b)/3> an which R1 and R2 are H, acyl, carbalkoxy, icarboxamido or N-substituted carboxamido or together form an aromatic hydrocarbon group which may be substituted by one or more alkyl, alkoxy or halogen substituents, and the other symbols are as before; the formula also includes 6 : 61-bis-benzthiazoles substituted in the 2 : 21-positions by -X-(Cn H2n) NR3 R4. Examples describe the preparation of benzthiazoles in which X is O or S, Cn H2n is ethylene, propylene or trimethylene and NR3 R4 is amino, dimethylamino, diethylamino, di-isopropylamino, ethyl-isopropylamino or ethyl-t-butylamino. Other compounds prepared are 2-(21-dimethylamino-ethylthio)-6-phenyl-benzthiazole, 2 : 21-bis-(21 dimethylamino - ethylthio) - 6 : 61-dibenzothiazole and 2-(21-diethylamino-ethylthio)-naphtho-[2,3]-thiazole. Starting materials are mentioned in which the benzthiazole nucleus is di- or poly-substituted. Ethyl 2-mercapto-thiazole-4-carboxylate is obtained from ethyl bromopyruvate and ammonium dithiocarbamate.ALSO:Fungicidal compositions comprise thiazoles of the formula: <FORM:0855389/VI/1> together with a finely-divided inert solid carrier or dispersed in an aqueous medium. In the formula R1 and R2 are H, acyl, carbalkoxy, carboxamide or N-substituted carboxamide, or together form an aromatic hydrocarbon group which may be substituted by halogen, alkyl or alkoxy; R3 and R4 are H or C1-C6 alkyl or together form a ring with the N atom; X is O or S; and n is 2-4; the formula also includes 6 : 61-bis-benzthiazoles substituted by the group -X(CnH2n) NR3R4 in the 2 : 21- positions. Suitable solid carriers are montmorillonite clays and talc, and a wetting agent can be incorporated in either the solid or the liquid compositions. The aqueous dispersions are prepared by diluting solutions in water-miscible solvents such as acetone.
GB10130/57A 1956-03-29 1957-03-29 Fungicidal compositions and basically substituted thiazoles for use therein Expired GB855389A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US855389XA 1956-03-29 1956-03-29

Publications (1)

Publication Number Publication Date
GB855389A true GB855389A (en) 1960-11-30

Family

ID=22192278

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10130/57A Expired GB855389A (en) 1956-03-29 1957-03-29 Fungicidal compositions and basically substituted thiazoles for use therein

Country Status (1)

Country Link
GB (1) GB855389A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2199463A1 (en) * 1971-10-27 1974-04-12 Syntex Corp
US4353916A (en) * 1977-01-17 1982-10-12 Sumitomo Chemical Company, Ltd. Benzothiazol-2-ones and phytopathogenic fungicidal use thereof
GB2161160B (en) * 1984-07-06 1989-05-24 Fisons Plc Heterocyclic sulphinyl compounds
EP0452076A1 (en) * 1990-04-09 1991-10-16 Meiji Seika Kabushiki Kaisha Thiazole and imidazole derivatives and antiulcer composition containing same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2199463A1 (en) * 1971-10-27 1974-04-12 Syntex Corp
US4353916A (en) * 1977-01-17 1982-10-12 Sumitomo Chemical Company, Ltd. Benzothiazol-2-ones and phytopathogenic fungicidal use thereof
GB2161160B (en) * 1984-07-06 1989-05-24 Fisons Plc Heterocyclic sulphinyl compounds
EP0452076A1 (en) * 1990-04-09 1991-10-16 Meiji Seika Kabushiki Kaisha Thiazole and imidazole derivatives and antiulcer composition containing same

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