FIELD: chemistry.
SUBSTANCE: invention relates to azolin compounds of formula I, where X1 is O; A is group 2; where A 2 represents a group -C(R7a)(R7b)-N(R52)-C(=O)-R62; B1, B2, B3, B4 and B5 independently represent CR2; Rg1 and Rg2 together form a bridging group selected from a group consisting of -CH2CH2O-, -OCH2CH2-, -CH2OCH2-, -OCH2O-, -CH2CH2S(O)p-, -S(O)pCH2CH2-, -CH2S(O)pCH2-, -OCH2CH2CH2- and -CH2CH2CH2O-; where p is 0, 1 or 2; R1 is C1-haloalkyl; each R2 is independently selected from a group consisting of hydrogen, halogen and C1-C2-haloalkyl; R3a and R3b are hydrogen; R7a and R7b are hydrogen; R52 is selected from a group consisting of hydrogen, C1-C3-alkyl and C1-C6-alkoxymethyl; R62 is selected from a group consisting of C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkyl, substituted with one or two radicals R82, C1-C6-haloalkyl, which carries one radical R82, C2-C6-alkynyl, C3-C6-cycloalkyl, which optionally carries CN substitute, C3-C6-halocycloalkyl, -CH=NOR92 and heterocyclic ring, selected from a group consisting of rings of formulas E-43–E-63 (see claim 1), where in the rings E-43–E-63 the broken line represents a point of attachment to the remaining molecule; k is 0, 1, 2 or 3; n is 0, 1 or 2; and R16 has values given below; each R82 is independently selected from a group consisting of C3-C6-cycloalkyl, which optionally carries CN substitute; C3-C6-halocycloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, and heterocyclic ring, selected from a group consisting of rings E-43 to E-63, as defined above; R92 is selected from C1-C6-alkyl and C1-C6-haloalkyl; and each R16 is independently selected from a group consisting of C1-C4-alkyl and C1-C4-haloalkyl; or two R16, present on same carbon atom of saturated ring, can together form =O; and stereoisomers thereof and agriculturally or veterinarily acceptable salts. Invention also relates to an insecticidal or arachnid composition based on said compounds.
EFFECT: technical result is obtaining novel compounds which can be used in agriculture for controlling invertebrate pests.
17 cl, 3 tbl, 7 ex
Title | Year | Author | Number |
---|---|---|---|
PYRAZOLE COMPOUNDS AND THEIR APPLICATION IN METHOD OF FIGHTING INVERTEBRATE PESTS, IN METHOD OF PROTECTION OF PLANT REPRODUCTION MATERIAL, IN METHOD OF TREATMENT OR PROTECTION OF ANIMALS AGAINST INVASION OR INFECTION, IN MATERIAL OF PLANT REPRODUCTION AND AGRICULTURAL COMPOSITIONS CONTAINING THEREOF | 2008 |
|
RU2516290C2 |
AZOLINES | 2015 |
|
RU2727307C2 |
METHOD OF PRODUCING PYRAZOLES | 2015 |
|
RU2712192C2 |
TRICYCLIDE PESTICIDE COMPOUNDS | 2019 |
|
RU2816690C2 |
SULPHONAMIDE COMPOUNDS POSSESSING TRPM8 ANTAGONIST ACTIVITY | 2012 |
|
RU2563030C2 |
METAL-BASED THIOPHENE PHOTODYNAMIC COMPOUNDS AND THEIR USE | 2013 |
|
RU2677855C2 |
NEW 5,6-DIHYDROPYRIDINE-2-ON COMPOUNDS APPLICABLE AS THROMBIN INHIBITORS | 2004 |
|
RU2335492C2 |
AVERMECTIN B1 AND AVERMEKTINE B1 MONOSACCHARIDE DERIVATIVES WITH ALKOXYMETHYL SUBSTITUTE IN THE POSITION 4"- OR 4'- | 2003 |
|
RU2330857C2 |
QUINAZOLINE COMPOUNDS | 2003 |
|
RU2365588C2 |
PYRROLE, DIAZOLE, TRIAZOLE OR TETRAZOLE DERIVATIVES SUITABLE FOR COMBATING ARTHROPODS | 2016 |
|
RU2777537C2 |
Authors
Dates
2021-02-10—Published
2015-12-21—Filed