Process for preparation of fungicidal compositions

Process for preparation of fungicidal compositions

  • CN 1,222,301 A
  • Filed: 07/29/1994
  • Published: 07/14/1999
  • Est. Priority Date: 08/11/1993
  • Status: Abandoned Application
First Claim
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1. method for preparing Fungicidal composition is characterized in that the azepine dioxane alkene of formula (I) is mixed with filler and/or surfactant:

  • Wherein alkane two bases that replace are chosen in the A representative wantonly, optional separately arlydene or the inferior heteroaryl that replaces of Ar;

    The E representative is with R on 2 1The 1-alkene-1 of base, 1-two bases, or on 2, be with R 22-azepine-1-the alkene-1 of base, 1-two bases, or on 1, be with R 1Base 3-oxa-or 3-thia-1-propylene-2,3-two bases, or the representative at 3Last band R is basic and be with R on 1 13-azepine-1-the propylene-2 of base, 3-two Base, or representative is with R on 1 21-azepine-1-the propylene-2 of base, 3-two Base, or representative is with R on 1 2The 3-oxa-or the 3-thia-1-azepine of base -propylene-2,3-two bases, or representative is being with the R base and is being with R on 1 on 3 21 of base, 3-diaza-1-propylene-2,3-two bases, or the optional replacement of representativeImino group,WhereinR represents alkyl,R 1Represent hydrogen, halogen, cyano group or optional separately alkyl, alkoxyl, the alkane sulphur that replaces Base, alkylamino or dialkyl amido,R 2Represent hydrogen, amino, cyano group or optional separately alkyl, alkoxyl, the alkane ammonia that replaces Base or dialkyl amido;

    WithR 3Represent hydrogen, cyano group or optional separately alkyl, alkenyl, alkynyl, the cycloalkanes that replaces Base or cycloalkyl-alkyl, G represent a singly-bound, oxygen or representative optional separately by halogen, hydroxyl, alkyl, haloAlkane two bases, olefin 2 base, oxa-olefin 2 base, alkynes two bases that alkyl or cycloalkyl replaces,Or represent one of following groups;

    -Q-CQ-,-CQ-Q-,-CH 2-Q-,-Q-CH 2-,-CQ-Q-CH 2-, -CH 2-Q-CQ-,-Q-CQ-CH 2-,-Q-CQ-Q-CH 2-,-N=N-, -S(O) n-,-CH 2-S(O) n-,-CQ-,-S(O) n-CH 2-, -C(R 4)=N-O-,-C(R 4)=N-O-CH 2-,-N(R 5)-, -CQ-N(R 5)-,-N(R 5)-CQ-,-Q-CQ-N(R 5)-, -N=C(R 4)-Q-CH 2-,-CH 2-O-N=C(R 4)-,-N(R 5)-CQ-Q-, -CQ-N (R 5)-CQ-Q-,-N (R 5)-CQ-Q-CH 2-,-CQ-CH 2-or -N=N-C(R 4)=N-O-, WhereinN represents 0,1 or 2 numeral;

    Q represents oxygen or sulphur;

    R 4Represent the optional separately alkyl that replaces of hydrogen, cyano group or representative, alkoxyl, alkylthio group, Alkylamino, dialkyl amido or cycloalkyl andR 5Represent the optional separately alkyl that replaces of hydrogen, hydroxyl, cyano group or representative, alkoxyl or Cycloalkyl and Z representative are at alkyl, alkenyl, alkynyl, cycloalkyl, aryl or the heterocyclic radical of optional replacement separately.

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