Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
  • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
  • A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
  • A01N43/647—Triazoles; Hydrogenated triazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
  • A01N43/647—Triazoles; Hydrogenated triazoles
  • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
  • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
  • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P33/00—Antiparasitic agents
  • A61P33/14—Ectoparasiticides, e.g. scabicides
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
  • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D419/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
  • C07D419/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D419/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
  • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
  • C07D513/04—Ortho-condensed systems

Definitions

• the invention relates to the technical field of crop protection agents, in particular that of herbicides for the selective control of weeds and grass weeds in crops. Specifically, this invention relates to substituted heteroarylpyrrolones and their salts, processes for their preparation and their use as herbicides.
• WO2016 / 071359 and WO2016 / 071360 disclose pyrrolones which carry heterocyclic substituents on the nitrogen, for example optionally also further substituted
• substituted pyrrolones and their herbicidal or pesticidal properties are described in CH633678, DE 2735841, DE, EP0297378, EP0334133, EP0339390 and EP0286816.
• WO2016 / 071361, WO2016 / 071362, WO2016 / 071363 and WO2016 / 071364 also describe substituted hydantoins which likewise carry heterocyclic substituents on the nitrogen, for example optionally further substituted isoxazolines.
• Selected specifically substituted 1,3,4-thiadiazolyl and l, 2,4-thiadiazolyl-2,5-Dioxoimidazoline and their herbicidal activity are in DE2247266.
• Active substances are described, for example, in WO2015 / 018434.
• heteroarylpyrrolones which are monosubstituted at the C-C double bond or their salts as herbicidally active compounds has not yet been described.
• singly substituted heteroarylpyrrolones or their salts as herbicides are particularly well suited to the C-C double bond.
• the present invention thus provides substituted heteroarylpyrrolones of the general formula (I) or salts thereof
• A, A, A are the same or different and are independently N (nitrogen) or the group CR 8 , but in no case more than two N atoms are adjacent, and wherein R 8 in the group CR 8 are the same or has different meanings as defined below,
• X and Y are independently CH or the group CR 1 , where
• X is CH when Y is the group CR 1 and
• X is the group CR 1 when Y is CH, R 1 is halogen, (Ci-C 8) -alkyl, (Ci-C 8) haloalkyl, (Ci-C8) hydroxyalkyl, (Ci-C 8) alkoxyalkyl, (Ci-C 8) alkoxy, (C 1 -C 8 ) -haloalkoxy, (C 1 -C 8 ) -alkylthio, (C 1 -C 8 ) -haloalkylthio, aryl,
• R 3 is hydroxy, hydrothio, halogen, (Ci-C 8) alkoxy, (C 3 -Cio) cycloalkyl- (Ci-C8) - alkoxy, aryl (Ci-C 8) alkoxy, (Ci-C 8) alkoxy (Ci C 8 ) -alkoxy, arylcarbonyloxy, (C 1 -C 8 ) -alkylcarbonyloxy, aryl- (C 1 -C 8 ) -alkylcarbonyloxy, heteroarylcarbonyloxy, (C 3 -C 10) -cycloalkylcarbonyloxy, heterocycliccarbonyloxy, (C 1 -C 8 ) -haloalkyl-carbonyloxy, (C 2 -C 8 ) alkenylcarbonyloxy, OC (O) OR 12 , OC (O) SR 12 , OC (S) OR 12 , OC (S) SR 12 ,
• R 4 and R 7 independently of one another represent hydrogen, hydrothio, hydroxy, halogen, (C 1 -C 8 ) -alkyl,
• a 2 and A 3 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally substituted by heteroatoms from the group N, O and S interrupted and if necessary further
• a 3 and A 4 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally substituted by heteroatoms from the group N, O and S interrupted and if necessary further
• R 11 are identical or different and are each independently hydrogen, (Ci-C 8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) alkynyl , (Ci-C 8) cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -C 8) -haloalkenyl, (C 2 -C 8) haloalkynyl, (C 3 -Cio) cycloalkyl, (C 3 -Cio) -halocycloalkyl, (C 4 -Cio) -cycloalkenyl, (C 4 -Cio) -halocycloalkenyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkoxy - (Ci-C 8)
• cyclic structural elements in particular the structural elements aryl, cycloalkyl,
• Alkoxy-carbonyl, (Ci-C 4) haloalkoxy-carbonyl, (Ci-C 4) -alkyl carboxy, (C3-C6) -cycloalkyl, (C3-C6) - cycloalkyl- (Ci-C6) alkyl, (C C 4 ) alkoxycarbonyl (Ci-C 4 ) alkyl, hydroxycarbonyl, hydroxycarbonyl (Ci-C 4 ) alkyl, R 10 R u N-carbonyl, and wherein the structural elements cycloalkyl or heterocyclyl n have oxo groups where n 0, 1 or 2.
• the compounds of general formula (I) can be prepared by addition of a suitable organic compound.
• inorganic or organic acid such as mineral acids such as HCl, HBr, H 2 S0 4 , H 3 PO 4 or HNO 3 , or organic acids, e.g.
• carboxylic acids such as formic acid, acetic acid, propionic acid, oxalic acid, lactic acid or salicylic acid or sulfonic acids such as p-toluenesulfonic acid to form a basic group such as amino, alkylamino, dialkylamino, piperidino, morpholino or pyridino, salts.
• These salts then contain the conjugate base of the acid as an anion.
• Sulfonklareamide or carboxylic acids may form internal salts with their turn protonatable groups, such as amino groups. Salt formation can also be due to the action of a base
• Suitable bases are, for example, organic amines, such as trialkylamines, morpholine, piperidine and pyridine and ammonium, alkali or
• Alkaline earth metal hydroxides, carbonates and bicarbonates in particular sodium and Potassium hydroxide, sodium and potassium carbonate and sodium and potassium bicarbonate.
• These salts are compounds in which the azide hydrogen is replaced by a cation suitable for agriculture, for example metal salts, in particular alkali metal salts or
• Alkaline earth metal salts in particular sodium and potassium salts, or else ammonium salts, salts with organic amines or quaternary ammonium salts, for example with cations of the formula
• R a to R d are each independently an organic radical, in particular alkyl, aryl, arylalkyl or alkylaryl. Also suitable are alkylsulfonium and
• Alkylsulfoxoniumsalze such as (Ci-C4) -trialkylsulfonium and (Ci-C4) -Trialkylsulfoxoniumsalze.
• the substituted heteroarylpyrrolones of the formula (I) according to the invention can be present in various tautomeric structures, all of which are intended to be encompassed by the general formula (I).
• the preferred subject of the invention are compounds of the general formula (I) in which Q represents the groups Q1 to Q-29
• a 1 , A 2 , A 3 , A 4 are the same or different and are each independently N (nitrogen) or the
• X and Y are independently CH or the group CR 1 , where X is CH when Y is the group CR 1 and
• X is the group CR 1 when Y is CH
• R 1 represents halogen, (C 1 -C 4) -alkyl, (C 1 -C 4) -haloalkyl, (C 1 -C 4) -hydroxyalkyl, (C 1 -C 4) -alkoxyalkyl,
• R 3 is hydroxy, hydrothio, halogen, NR 1, R 1 (C 1 -C 4) -alkoxy, (C 3 -C 10) -cycloalkyl- (C 1 -C 7 ) -alkoxy, aryl- (C 1 -C 4) -alkoxy, ( C 1 -C 7) -alkoxy- (C 1 -C 4) -alkoxy, arylcarbonyloxy, (C 1 -C 7) -alkylcarbonyloxy, aryl- (C 1 -C 7) -alkylcarbonyloxy, heteroarylcarbonyloxy, (C 3 -C 10) -cycloalkylcarbonyloxy, heterocycliccarbonyloxy, C7) haloalkyl-carbonyloxy, (C2-C7) - alkenylcarbonyloxy, OC (0) OR12, OC (0) SR 12, OC (S) OR 12, OC (S) SR 12, O
• R 4 and R 7 independently of one another represent hydrogen, hydrothio, hydroxyl, halogen, (C 1 -C 7 ) -alkyl,
• Q for Q-3, Q-4, Q-8, Q-9, Q-12 and Q-19 is hydrogen, formyl, (C 1 -C 4) -alkyl, (C 1 -C 4) -haloalkyl, hydroxy (C 1 -C 4) -alkyl,
• a 2 and A 3 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally substituted by heteroatoms from the group N, O and S interrupted and if necessary further
• a 3 and A 4 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally substituted by heteroatoms from the group N, O and S interrupted and if necessary further
• R 11 are identical or different and are each independently hydrogen, (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl , (Ci-C 7) cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) haloalkynyl, (C 3 -Cio) cycloalkyl, (C 3 -Cio) -halocycloalkyl, (C 4 -Cio) -cycloalkenyl, (C 4 -Cio) -halocycloalkenyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkoxy - (Ci-C 7 )
• R is (Ci-Cv) -alkyl, (C 2 -C 7 ) -alkenyl, (C 2 -C 7 ) -alkynyl, (Ci-Cv) -cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 - C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 10) -cycloalkyl, (C 3 -C 10) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) - Halocycloalkenyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, aryl, ary
• W is oxygen or sulfur.
• A, A, A are the same or different and are independently N (nitrogen) or the group CR 8 , but in no case more than two N atoms are adjacent, and wherein R 8 in the group CR 8 are the same or has different meanings as defined below,
• X and Y are independently CH or the group CR 1 , where
• X is CH when Y is the group CR 1 and
• X is the group CR 1 when Y is CH, R 1 is halogen, (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -hydroxyalkyl, (C 1 -C 6 ) -alkoxyalkyl, (C 1 -C 6 ) -alkoxy, (C 1 -C 6 ) -haloalkoxy, (C 1 -C 6 ) -alkylthio, (C 1 -C 6 ) -haloalkylthio, aryl,
• R 3 is hydroxy, hydrothio, halogen, (C 1 -C 6 ) -alkoxy, (C 3 -C 10) -cycloalkyl- (C 1 -C 6 ) -alkoxy, aryl- (C 1 -C 6 ) -alkoxy, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkoxy, arylcarbonyloxy, (C 1 -C 6) -alkylcarbonyloxy, aryl- (C 1 -C 6) -alkylcarbonyloxy, heteroarylcarbonyloxy, (C 3 -C 10) -cycloalkylcarbonyloxy, heterocycliccarbonyloxy, (C 1 -C 6) -haloalkylcarbonyloxy, (C 2 -C 6) Alkenylcarbonyloxy, OC (O) OR 12 , OC (0) SR 12 , OC (S) OR
• R 4 and R 7 independently of one another represent hydrogen, hydrothio, hydroxyl, halogen, (C 1 -C 6) -alkyl,
• a 2 and A 3 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally substituted by heteroatoms from the group N, O and S interrupted and if necessary further
• a 3 and A 4 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally substituted by heteroatoms from the group N, O and S interrupted and if necessary further
• R 11 are identical or different and independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (Ci-C6) cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -C 6) haloalkenyl, (C 2 -C 6) haloalkynyl, (C 3 -Cio) cycloalkyl, (C 3 - Cio) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkoxy, (C 1 -C 6 )
• R is (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 10) -cycloalkyl, (C 3 -C 10) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -Cio ) -Halocycloalkenyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl-
• W is oxygen or sulfur.
• a 1 , A 2 , A 3 , A 4 are the same or different and are each independently N (nitrogen) or
• Grouping CR 8 but in no case more than two N atoms are adjacent, and wherein R 8 in the group CR 8 each have the same or different meanings as defined above, X and Y are independently CH or the grouping CR 1 stand, where
• X is CH when Y is the group CR 1 and X is the group CR 1 when Y is CH,
• R 1 is fluorine, chlorine, bromine, iodine, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2 Methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1 , 1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1, 1, 2 Tri
• Trifluoromethylthio-phenyl 4-trifluoromethylthio-phenyl, phenyloxy, p-Cl-phenyloxy,
• Cyclohexylmethyl methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, iso-propylcarbonyl, n-butylcarbonyl, tert-butylcarbonyl, ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1
• R 4 and R 7 independently of one another represent hydrogen, fluorine, chlorine, bromine, iodine, hydroxyl, hydrothio, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1- Dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2- Methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1 - Ethyl
• Fluoromethyl difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, difluoro-tert-butyl,
• Benzylmethylaminocarbonyl methylamino, dimethylamino, ethylamino, diethylamino, n-propylamino, iso-propylamino, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, benzylamino, cyanomethyl, cyanoethyl, 3-cyanoprop-1-yl, 2-cyanoprop-1-yl, 1 Cyanoprop-1-yl, 2-cyanoprop-2-yl, 2-cyano-1, 1-dimethyleth-1-yl, 1 - (cyanomethyl) -1-methylprop-1-yl, hydroxycarbonyl, hydroxycarbonylmethyl, hydroxycarbonylethyl, CHO, Methoxyethylthio, ethoxyethylthio, trifluoromethoxyethylthio, pentafluoroethoxyeth
• Q for Q-3, Q-4, Q-8, Q-9, Q-12 and Q-19 is hydrogen, formyl, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n- Pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3 Methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-d
• Methoxycarbonylmethyl ethoxycarbonylmethyl, n-propyloxycarbonylmethyl, isopropyloxycarbonylmethyl, tert-butyloxycarbonylmethyl, methoxycarbonylethyl,
• Methylaminocarbonyloxy ethylaminocarbonyloxy, n-propylaminocarbonyloxy, isopropylaminocarbonyloxy, benzylaminocarbonyloxy, phenylaminocarbonyloxy,
• Cyclohexylmethyl trifluoromethyl, pentafluoroethyl, 1,1,2,2-tetrafluoroethyl, heptafluoro-n-propyl, heptafluoro-isopropyl, nonafluorobutyl, chlorodifluoromethyl, bromodifluoromethyl, dichlorofluoromethyl, iododifluoromethyl, bromofluoromethyl, 1-fluoroethyl, 2-fluoroethyl,
• Fluoromethyl difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, difluoro-tert-butyl,
• Chloromethyl bromomethyl, fluoromethyl, 3,3,3-trifluoro-n-propyl, methoxycarbonyl,
• Ethoxycarbonyl iso-propyloxycarbonyl, n-propyloxycarbonyl, n-butyloxycarbonyl, tert-butyloxycarbonyl, benzyloxycarbonyl, allyloxycarbonyl, methylaminocarbonyl,
• Methylaminosulfonylamino dimethylaminosulfonylamino, ethylaminosulfonylamino, diethylaminosulfonylamino, iso-propylaminosulfonylamino, cyclopropylaminosulfonylamino, cyclobutylaminosulfonylamino, cyclopentylaminosulfonylamino,
• a 2 and A 3 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally Heteroatoms from the group N, O and S interrupted and optionally further
• a 3 and A 4 when both represent a group CR 8 , with the atoms to which they are attached, a partially saturated or fully unsaturated, optionally
• W stands for oxygen
• X is CH when Y is the group CR 1 and
• X is the group CR 1 when Y is CH
• R 1 represents chlorine, bromine, iodine, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl , 3-methylbutyl, 1,1-
• Dimethylpropyl 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1, 1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl,
• Difluoromethylcarbonyloxy methoxycarbonyloxy, ethoxycarbonyloxy, n-propyloxycarbonyloxy, iso -propyloxycarbonyloxy, n-butyloxycarbonyloxy, 1,1-dimethylethyloxycarbonyloxy, 2,2-dimethylpropyloxycarbonyloxy, pyridin-2-ylcarbonyloxy, pyridin-3-ylcarbonyloxy, pyridin-4-ylcarbonyloxy, 4-trifluoromethylpyridine-3-butylcarbonyloxy, allylcarbonyloxy, methylsulfonyloxy, ethylsulfonyloxy, n-propylsulfonyloxy, 1-methylethylsulfonyloxy, cyclopropylsulfonyloxy, is hydrogen, is oxygen and is one of the groupings Q1 specifically mentioned in the table below. l to Q-29.5 says:
• X and Y are independently CH or the group CR 1 , where
• X is CH when Y is the group CR 1 and
• X is the group CR 1 when Y is CH
• R 1 is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-
• Adamantan-2-yl 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-dimethylcyclopropyl, 1'-bi (cyclopropyl) -1-yl, 1'-bi (cyclopropyl) - 2-yl, 2'-methyl-1, 1'-bi (cyclopropyl) -2-yl, 1-cyanocyclopropyl, 2-cyanocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 3-methylcyclobutyl, 3,3-dimethylcyclobut-1 -yl, 3,3-difluorocyclobut-1-yl, 3-fluorocyclobut-1-yl, 2,2-difluorocycloprop-1-yl, 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, 1-ethylcyclopropyl , 1-methylcyclohexyl, 2-methylcycl
• Difluoromethylcarbonyloxy methoxycarbonyloxy, ethoxycarbonyloxy, n-propyloxycarbonyloxy, iso -propyloxycarbonyloxy, n-butyloxycarbonyloxy, 1,1-dimethylethyloxycarbonyloxy, 2,2-dimethylpropyloxycarbonyloxy, pyridin-2-ylcarbonyloxy, pyridin-3-ylcarbonyloxy, pyridin-4-ylcarbonyloxy, 4-trifluoromethylpyridine-3-butylcarbonyloxy, allylcarbonyloxy, methylsulfonyloxy, ethylsulfonyloxy, n-propylsulfonyloxy, 1-methylethylsulfonyloxy, cyclopropylsulfonyloxy, is hydrogen, is oxygen and
• Q is one of the groupings Q-1.1 to Q-29.5 mentioned specifically in the table above, particularly preferably the radicals Q-8.7 listed in the table above,
• Q-13.5 and Q-16.61 are excluded if X is C-methyl or C-methoxy and in both cases Y is simultaneously C-H.
• alkylsulfonyl alone or as part of a chemical group - is straight-chain or branched alkylsulfonyl, preferably with 1 to 8, or with 1 to 6
• Carbon atoms e.g. (but not limited to) (C 1 -C 6) alkylsulfonyl such as methylsulfonyl, ethylsulfonyl, propylsulfonyl, 1-methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl, 2-methyl-propylsulfonyl, 1,1-dimethylethylsulfonyl, pentylsulfonyl, 1-methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 1,1-dimethylpropylsulfonyl, 1, 2-dimethylpropylsulfonyl, 2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl, 1-methylpent
• heteroarylsulfonyl is optionally substituted pyridylsulfonyl
• Heteroarylsulfonyl here in particular optionally substituted quinolinylsulfonyl, for example substituted by fluorine, chlorine, bromine, iodine, cyano, nitro, alkyl, haloalkyl, haloalkoxy, amino, alkylamino, alkylcarbonylamino, dialkylamino or alkoxy groups.
• alkylthio alone or as part of a chemical group - is straight-chain or branched S-alkyl, preferably with 1 to 8, or with 1 to 6
• Carbon atoms such as (Ci-Cio) -, (CI-C ⁇ ) - or (Ci-C4) -alkylthio, e.g. (but not limited to) (ce-Ce) -alkylthio, such as methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio, 1, 1-dimethylethylthio, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 1, 1-dimethylpropylthio, 1, 2-dimethylpropylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1, 1 Dimethylbuty
• alkenylthio denotes an alkenyl radical bonded via a sulfur atom
• alkynylthio represents an alkynyl radical bonded via a sulfur atom
• cycloalkylthio denotes a cycloalkyl radical bonded via a sulfur atom
• cycloalkenylthio denotes an via
• Alkoxy means an alkyl radical bonded through an oxygen atom, for example (but not limited to) (C 1 -C 6) alkoxy, such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy, 1 , 1-Dimethylethoxy, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy , 3-methylpentoxy, 4-methylpentoxy, 1, 1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy , 2-ethylbutoxy, 1, 1,2-trimethylpropoxy, 1, 2,2-trimethylpropoxy, 1-ethylbutoxy
• Alkenyloxy means an alkenyl radical bonded through an oxygen atom
• alkynyloxy means an above an oxygen atom bonded alkynyl group such as (C 2 -C 1 0) -, (C 2 -C 6) - or (C 2 -C 4) alkenoxy, and (C3-C10) -, (C 3 -C 6) - or (C 3 -C 4 ) -alkoxy.
• Cycloalkyloxy denotes a cycloalkyl radical bonded via an oxygen atom and cycloalkenyloxy denotes a cycloalkenyl radical bonded via an oxygen atom.
• the number of C atoms refers to the alkyl radical in the
• the number of C atoms refers to the alkenyl or alkynyl radical in the alkenyl or alkynylcarbonyl group.
• the number of C atoms here refers to the alkyl radical in the alkoxycarbonyl group, analogously “alkenyloxycarbonyl” and “alkynyloxycarbonyl”, unless otherwise defined elsewhere, according to the invention for alkenyl or alkynyl radicals which are bonded to the skeleton via -O-C ( O), such as (C 2 -C 10) -, (C 2 -C 6 ) - or (C 2 -C 4 ) - alkenyloxycarbonyl or (C3-C10) -, (C 3 -C 6) - or (C3-C4) -
• the number of C atoms refers to the alkyl radical in the alkylcarbonyloxy group.
• the number of C atoms refers to the alkenyl or alkynyl radical in the alkenyl or alkynylcarbonyloxy group.
• C (O) R 12 C (O) OR 12 , OC (O) NR 10 R u , or C (O) NR 10 R u
• the short form O shown in parentheses represents a double bond to the adjacent carbon atom bound oxygen atom.
• aryl means an optionally substituted mono-, bi- or polycyclic aromatic system having preferably 6 to 14, in particular 6 to 10 ring C atoms, for example phenyl, naphthyl, anthryl, phenanthrenyl, and the like, preferably phenyl.
• optionally substituted aryl also includes polycyclic systems, such as
• Preferred aryl substituents here are, for example, hydrogen, halogen, alkyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, halocycloalkyl, alkenyl, alkynyl, aryl, arylalkyl, arylalkenyl, heteroaryl, heteroarylalkyl, heterocyclyl, heterocyclylalkyl, alkoxyalkyl, alkylthio, haloalkylthio, haloalkyl, alkoxy, Haloalkoxy, cycloalkoxy, cycloalkylalkoxy, aryloxy, heteroaryloxy, alkoxyalkoxy, alkynylalkoxy, alkenyloxy, bis-alkylaminoalkoxy, tris [alkyl] silyl, bis [alkyl] arylsilyl, bis [alkyl] alkylsilyl, tris [alkyl
• Alkylaminocarbonyl cycloalkylaminocarbonyl, bis-alkylaminocarbonyl, heteroarylalkoxy,
• heterocyclyl or heterocyclic ring is optionally substituted, it may be fused with other carbocyclic or heterocyclic rings.
• polycyclic systems are also included, for example 8-azabicyclo [3.2.1] octanyl, 8-azabicyclo [2.2.2] octanyl or 1-azabicyclo [2.2.1] heptyl.
• optionally substituted heterocyclyl also become
• the heterocyclic ring preferably contains 3 to 9 ring atoms, in particular 3 to 6 ring atoms, and one or more, preferably 1 to 4, in particular 1, 2 or 3 heteroatoms in the heterocyclic ring, preferably from the group N, O, and S, but not two
• Oxygen atoms are to be directly adjacent, such as with a heteroatom from the group N, O and S 1- or 2- or 3-pyrrolidinyl, 3,4-dihydro-2H-pyrrol-2 or 3-yl, 2,3- dihydro-lH-pyrrole
• heterocyclyl are a partially or fully hydrogenated heterocyclic radical having two heteroatoms from the group N, O and S, such as 1- or 2- or 3- or 4-pyrazolidinyl; 4,5-dihydro-3H-pyrazole-3 or 4 or 5-yl; 4,5-dihydro-1H-pyrazole-1- or 3- or 4- or 5-yl; 2,3-dihydro-1H-pyrazole-1 or 2 or
• Hexahydropyrimidine-1 or 2 or 3 or 4-yl 1,4,5,6-tetrahydropyrimidine-1- or 2- or 4- or 5- or 6-yl; 1,2,5,6-tetrahydropyrimidine-1- or 2- or 4- or 5- or 6-yl; 1,2,3,4
• heterocyclyl are a partially or fully hydrogenated heterocyclic radical having 3 heteroatoms from the group N, O and S, such as, for example, l, 4,2-dioxazolidin-2 or 3 or 5-yl; l, 4,2-dioxazol-3 or 5-yl; 1,2,2-dioxazinane-2- or -3- or 5- or 6-yl; 5,6-dihydro-l, 4,2-dioxazine-3 or 5 or 6-yl; l, 4,2-dioxazine-3- or 5- or 6-yl; l, 4,2-dioxazepan-2 or 3 or 5 or 6 or 7-yl; 6,7-dihydro-5H-l, 4,2-dioxazepine-3 or 5 or 6 or 7-yl; 2,3-dihydro-7H-l, 4,2-dioxazepin-2 or 3 or 5 or 6 or 7-yl; 2,3-dihydro-5H-1,
• heterocycles listed above are preferably, for example, hydrogen, halogen, alkyl, haloalkyl, hydroxy, alkoxy, cycloalkoxy, aryloxy, alkoxyalkyl, alkoxyalkoxy, cycloalkyl,
• Alkylaminocarbonyl bis-alkylaminocarbonyl, cycloalkylaminocarbonyl,
• Suitable substituents for a substituted heterocyclic radical are the substituents mentioned below, in addition to oxo and thioxo.
• the oxo group as a substituent on a ring C atom then means, for example, a carbonyl group in the heterocyclic ring.
• lactones and lactams are preferably also included.
• the oxo group may also be attached to the hetero ring atoms, which may exist in different oxidation states, e.g. For example, at N and S, the divalent groups N (O), S (O) (also SO for short) and S (O) 2 (also SO2 for short) occur and form in the heterocyclic ring.
• N (O) and -S (0) groups both enantiomers are included.
• heteroaryl stands for heteroaromatic compounds, ie.
• heteroaryls are, for example, 1H-pyrrol-1-yl; lH-pyrrol-2-yl; lH-pyrrole
• Carbon atoms part of another aromatic ring they are fused heteroaromatic systems, such as benzo-fused or multiply fused heteroaromatic.
• quinolines e.g., quinolin-2-yl, quinolin-3-yl, quinolin-4-yl, quinolin-5-yl, quinolin-6-yl, quinolin-7-yl, quinolin-8-yl
• Isoquinolines e.g., isoquinolin-1-yl, isoquinolin-3-yl, isoquinolin-4-yl, isoquinolin-5-yl, isoquinolin-6-yl, isoquinolin-7-yl, isoquinolin-8-yl
• quinoxaline quinazoline
• cinnoline 1,5-naphthyridine; 1,6-naphthyridine; 1,7-naphthyridine; 1,8-naphthyridine; 2,6- naphthyridine; 2,7-naphthyridine; phthalazine; Pyridopyrazine;
• heteroaryl are also 5- or 6-membered benzo-fused rings from the group 1H-indol-1-yl, 1H-indol-2-yl, 1H-indol-3-yl, 1H-indol-4-yl, 1H- Indol-5-yl, 1H-indol-6-yl, 1H-indol-7-yl, 1-benzofuran-2-yl, 1-benzofuran-3-yl, 1-benzofuran-4-yl, 1-benzofuran 5-yl, 1-benzofuran-6-yl, 1-benzofuran-7-yl, 1-benzothiophen-2-yl, 1-benzothiophen-3-yl, 1
• halogen means, for example, fluorine, chlorine, bromine or iodine.
• halogen means, for example, a fluorine, chlorine, bromine or iodine atom.
• alkyl means a straight-chain or branched, open-chain, saturated hydrocarbon radical which is optionally monosubstituted or polysubstituted and is referred to in the latter case as “substituted alkyl".
• Preferred substituents are halogen atoms, alkoxy, haloalkoxy, cyano, alkylthio, haloalkylthio, amino or nitro groups, particularly preferred are methoxy, methyl, fluoroalkyl, cyano, nitro, fluorine, chlorine, bromine or iodine.
• the prefix "bis” also includes the combination of different alkyl radicals, for example, methyl (ethyl) or ethyl (methyl).
• Haloalkyl means by the same or different halogen atoms, partially or fully substituted alkyl, alkenyl and alkynyl, for example monohaloalkyl
• ( Monohaloalkyl) such. CH 2 CH 2 Cl, CH 2 CH 2 Br, CHClCH 3 , CH 2 Cl, CH 2 F; Perhaloalkyl such. B. CCl 3, CC1F 2, CFC1 2 CF 2 CC1F 2, CF 2 CC1FCF 3; Polyhaloalkyl such. CH 2 CHFC1, CF 2 CC1FH, CF 2 CBrFH, CH 2 CF 3; The term perhaloalkyl also encompasses the term perfluoroalkyl.
• Partially fluorinated alkyl means a straight-chain or branched, saturated hydrocarbon which is monosubstituted or polysubstituted by fluorine, wherein the corresponding fluorine atoms as substituents on one or more different carbon atoms of the straight-chain or branched hydrocarbon chain can be located, such as. B. CHFCH3, CH2CH2F, CH2CH2CF3, CHF 2, CH 2 F, CHFCF2CF3
• Partially fluorinated haloalkyl means a straight-chain or branched, saturated one
• Hydrocarbon which is substituted by various halogen atoms having at least one fluorine atom, wherein all other optional halogen atoms are selected from the group fluorine, chlorine or bromine, iodine.
• the corresponding halogen atoms may be present as substituents on one or more different carbon atoms of the straight-chain or branched hydrocarbon chain.
• Partially fluorinated haloalkyl also includes the complete substitution of halogen with the participation of at least one fluorine atom of the straight-chain or branched chain.
• Haloalkoxy is, for example, OCF 3 , OCHF 2 , OCH 2 F, OCF 2 CF 3 , OCH 2 CF 3 and OCH 2 CH 2 Cl, and the same applies to haloalkenyl and other halogen-substituted radicals.
• (C 1 -C 4) -alkyl denotes a short notation for straight-chain or branched alkyl having one to four carbon atoms corresponding to the formula
• Range indication for C atoms, d. H. includes the radicals methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methylpropyl or tert-butyl.
• General alkyl radicals having a larger specified range of carbon atoms eg. As "(Ci-C6) alkyl", accordingly also include straight-chain or branched alkyl radicals having a larger number of C atoms, d. H. according to example, the alkyl radicals with 5 and 6 carbon atoms.
• hydrocarbon radicals such as alkyl, alkenyl and alkynyl radicals, even in assembled radicals, are the lower carbon skeletons, e.g. with 1 to 6 C atoms or with unsaturated groups having 2 to 6 C atoms, preferred.
• Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals, wherein at least one double bond or triple bond is contained. Preference is given to radicals having a double bond or
• alkenyl in particular also includes straight-chain or branched open-chain
• Hydrocarbon radicals having more than one double bond such as 1,3-butadienyl and 1,4-pentadienyl, but also allenyl or cumulenyl radicals having one or more cumulated double bonds, such as allenyl (1,2-propadienyl), 1, 2-butadienyl and 1,2,3-pentatrienyl.
• Alkenyl means eg Vinyl, which may optionally be substituted by further alkyl radicals, for example (but not limited to) (C 2 -C 6) -alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2- Butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl,
• alkynyl in particular also includes straight-chain or branched open-chain
• C 2 -C 6) -alkynyl is, for example, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3 Pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1, 1-dimethyl-2-propynyl, 1 Ethyl 2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl,
• cycloalkyl means a carbocyclic, saturated ring system preferably having 3-8 ring C atoms, eg cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, which is optionally further substituted, preferably by hydrogen, alkyl, alkoxy, cyano, nitro, alkylthio , Haloalkylthio, halogen, alkenyl, alkynyl, haloalkyl, amino, alkylamino, bisalkylamino, alkocycarbonyl,
• Cycloalkylaminocarbonyl In the case of optionally substituted cycloalkyl cyclic systems are included with substituents, wherein substituents having a double bond on Cycloalkyl, z.
• substituents having a double bond on Cycloalkyl, z As an alkylidene group such as methylidene, are included.
• polycyclic aliphatic systems are also included, such as, for example, bicyclo [1,1.0] butan-1-yl, bicyclo [1,1-0] butan-2-yl, bicyclo [2.1.0] pentan-1-yl , Bicyclo [1,11] pentan-1-yl, bicyclo [2.1.0] pentan-2-yl, bicyclo [2.1.0] pentan-5-yl, bicyclo [2.1.1] hexyl, bicyclo [2.2.1 ] hept-2-yl, bicyclo [2.2.2] octan-2-yl, bicyclo [3.2.1] octan-2-yl, bicyclo [3.2.2] nonan-2-yl, adamantan-1-yl and
• spirocyclic aliphatic systems are also included, such as spiro [2.2] pent-1-yl, spiro [2.3] hex-1-yl, spiro [2.3] hex-4-yl, 3-spiro [2.3] hex-5-yl, spiro [3.3] hept-1-yl, spiro [3.3] hept-2-yl.
• Cycloalkenyl means a carbocyclic, non-aromatic, partially unsaturated ring system preferably having 4-8 C atoms, eg 1-cyclobutenyl, 2-cyclobutenyl, 1-cyclopentenyl, 2-cyclopentenyl, 3-cyclopentenyl, or 1-cyclohexenyl, 2- Cyclohexenyl, 3-cyclohexenyl, 1,3-cyclohexadienyl or 1,4-cyclohexadienyl, substituents also having a double bond on the cycloalkenyl radical, eg an alkylidene group such as methylidene, being included
• the explanations apply to substituted Corresponding to cycloalkyl.
• Cycloalkylalkyloxy means a cycloalkylalkyl radical bonded via an oxygen atom
• arylalkyloxy means an arylalkyl radical bonded via an oxygen atom
• Alkoxyalkyl means an alkoxy group attached via an alkyl group
• alkoxyalkoxy means an alkoxyalkyl group bonded via an oxygen atom, e.g. (but not limited to) methoxymethoxy, methoxyethoxy, ethoxyethoxy, methoxy-n-propyloxy.
• Alkylthioalkyl means an alkylthio radical bonded via an alkyl group and
• Alkylthioalkylthio means an alkylthioalkyl radical bonded via an oxygen atom.
• Arylalkoxyalkyl means an aryloxy group bonded through an alkyl group, and “heteroaryloxyalkyl” means a heteroaryloxy group bonded via an alkyl group.
• Haloalkoxyalkyl means a haloalkoxy radical attached and "haloalkylthioalkyl” means a haloalkylthio radical attached via an alkyl group.
• Arylalkyl means an aryl group attached via an alkyl group
• heteroarylalkyl means a heteroaryl group bonded via an alkyl group
• heterocyclylalkyl means a heterocyclyl group bonded through an alkyl group.
• Cycloalkylalkyl means a cycloalkyl radical attached via an alkyl group, for example (but not limited to) cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 1-cyclopropyleth-1-yl, 2-cyclopropyleth-1-yl, 1-cyclopropylpropyl l-yl, 3-cyclopropylprop-1-yl.
• Arylalkenyl means an aryl group attached via an alkenyl group
• heteroarylalkenyl means a heteroaryl group attached via an alkenyl group
• heterocyclylalkenyl means a heterocyclyl group bonded via an alkenyl group
• Arylalkynyl means an aryl group bonded through an alkynyl group
• heteroarylalkynyl means a heteroaryl group bonded via an alkynyl group
• heterocyclylalkynyl means a heterocyclyl group bonded through an alkynyl group
• haloalkylthio alone or as part of a chemical group - is straight-chain or branched S-haloalkyl, preferably with 1 to 8, or with 1 to 6
• Carbon atoms such as (Ci-Cs) -, (CI-C ⁇ ) - or (Ci-C4) haloalkylthio, e.g. (but not limited to) trifluoromethylthio, pentafluoroethylthio, difluoromethyl, 2,2-difluoroeth-1-ylthio, 2,2,2-difluoroeth-1-ylthio, 3,3,3-prop-1-ylthio.
• haloalkylthio e.g. (but not limited to) trifluoromethylthio, pentafluoroethylthio, difluoromethyl, 2,2-difluoroeth-1-ylthio, 2,2,2-difluoroeth-1-ylthio, 3,3,3-prop-1-ylthio.
• Halocycloalkyl and “Halocycloalkenyl” mean by the same or different halogen atoms, such as. B. F, Cl and Br, or by haloalkyl, such as. Trifluoromethyl or difluoromethyl, partially or fully substituted cycloalkyl or cycloalkenyl, e.g.
• “trialkylsilyl” - alone or as part of a chemical group - is straight-chain or branched Si-alkyl, preferably with 1 to 8, or with 1 to 6 Carbon atoms, such as tri - [(Ci-Cs) -, (CI-C ⁇ ) - or (Ci-C4) -alkyl] silyl, for example (but not limited to) trimethylsilyl, triethylsilyl, tri (n-propyl) silyl, Tri (isopropyl) silyl, tri (n-butyl) silyl, tri (1-methylprop-1-yl) silyl, tri (2-methylprop-1-yl) silyl, tri (1, l) Dimethyleth-1-yl) silyl, tri (2,2-dimethyl-1-yl) silyl.
• Trialkylsilylalkinyl stands for a trialkylsilyl radical bonded via an alkynyl group.
• Compound of formula (I) are included.
• the compounds of the general formula (I) can exist as stereoisomers.
• the possible stereoisomers defined by their specific spatial form, such as enantiomers, diastereomers, Z and E isomers, are all encompassed by the formula (I). If, for example, one or more alkenyl groups are present, diastereomers (Z and E isomers) can occur. For example, if one or more asymmetric carbon atoms are present, enantiomers and diastereomers may occur.
• Stereoisomers can be distinguished from those in the
• stereoisomers can be selectively prepared by using stereoselective reactions using optically active sources and / or adjuvants.
• the invention thus also relates to all stereoisomers which comprises the general formula (I) but are not specified with their specific stereoform, and mixtures thereof.
• the purification can also by
• Suitable isolation, purification and stereoisomer separation methods of compounds of formula (I) are those which are well known to those skilled in the art from analogous cases, e.g. through physical processes such as crystallization, chromatography, especially
• any remaining mixtures can be separated, as a rule, by chromatographic separation, for example on chiral solid phases.
• Suitable for preparative amounts or on an industrial scale are processes such as crystallization, for example diastereomeric salts, which can be obtained from the diastereomer mixtures with optically active acids and optionally in the presence of acidic groups having optically active bases.
• the first key intermediate for the synthesis of the compounds of the general formula (I) according to the invention is an optionally further substituted heteroaromatic amine Q-NF.
• Q-NF an optionally further substituted heteroaromatic amine
• this is shown in the synthesis of an optionally further substituted 5-amino-l, 2,4-isothiazole (III).
• a substituted nitrile is converted into the corresponding amidine (for example with ammonia) and after halogenation with a suitable halogenating reagent (for example sodium hypochlorite or bromine) by reaction with potassium thiocyanate into the desired 5-amino-1, 2,4 -isothiazole (purple) transferred.
• a suitable halogenating reagent for example sodium hypochlorite or bromine
• potassium thiocyanate into the desired 5-amino-1, 2,4 -isothiazole (purple) transferred.
• bromochlorothiadiazole (IVa) can be prepared by amination, amino group protection (eg, with (Boc) 20, where Boc is tert-butyloxycarbonyl), followed by transition metal-mediated coupling reaction (with a suitable transition metal catalyst such as PdCl2 [P t Bu2 (FIG.
• a heteroaromatic amine Q-NH 2 is further described by the example of the preparation of optionally further substituted amino-1, 2,4-triazoles (see Scheme 2).
• a suitable reagent eg, an alkyl iodide
• a suitable polar aprotic solvent eg, ⁇ , ⁇ -dimethylformamide
• a suitable nitrotriazole (IVb) may be converted to the desired N-substituted by substitution of the ring nitrogen and subsequent hydrogenation with a suitable transition metal catalyst (eg, palladium or platinum on carbon) in a suitable solvent (eg, acetic acid or dilute hydrochloric acid) Aminotriazole (Illb) are converted (see Synthesis 2003, 2001, Tetrahedron Lett 2005, 46, 2469). In Scheme 2 below, R 4 and R 7 have the meanings defined above.
• a suitable transition metal catalyst eg, palladium or platinum on carbon
• a suitable solvent eg, acetic acid or dilute hydrochloric acid
• Simple monosubstituted heteroarylpyrrolones of general formula (I) can be prepared in two steps by reacting a suitable optionally substituted heteroarylamine Q-NH 2 (III) with a suitable optionally further substituted maleic anhydride (V) using a suitable base (e.g., pyridine) in a suitable polar aprotic solvent (e.g., acetonitrile) or under acidic conditions using a suitable acid (e.g., acetic acid or p-toluenesulfonic acid in toluene as solvent) and subsequent reduction of a carbonyl group of the substituted maleimideimide (II) formed.
• the reduction can be carried out in a suitable solvent (eg tetrahydrofuran and methanol) with the aid of a suitable solvent
• Suitable reducing agents are, for example, sodium hydride, lithium aluminum hydride, sodium borohydride or other hydrogen-forming metal hydrides. It can alternatively also a
• R 4 of the general formula (I) is tert-butyl
• R 5 is the general formula (I) is methyl
• R 7 is the general formula (I) is hydrogen
• R 1 of the general formula (I) is in each case by way of example, but not by way of limitation, for methyl.
• monosubstituted heteroarylpyrrolones of general formula (Ia) can be prepared starting from the reaction of a hydroxy or bromolactone (VII) with a suitable optionally substituted heteroarylamine Q-NF (III) in a suitable solvent (eg toluene) at elevated temperature become. Further reaction of the resulting intermediate (VIII) with acetic anhydride using a suitable base (e.g., pyridine) at elevated temperature forms the monosubstituted heteroarylpyrrolone of general formula (IX) with O-acetyl group by heating under acidic conditions (For example, in a mixture of acetic acid and
• acylated with suitable reagents eg, using a suitable carbonyl chloride and with the aid of a suitable base such as triethylamine in a suitable polar aprotic solvent
• suitable reagents eg, using a suitable carbonyl chloride and with the aid of a suitable base such as triethylamine in a suitable polar aprotic solvent
• sulfonylated e.g., using a suitable sulfonyl chloride and A suitable base such as triethylamine in a suitable polar aprotic solvent
• alkylated eg using a suitable alkyl halide and with the aid of a suitable base such as potassium carbonate, cesium carbonate or sodium hydride in a suitable polar aprotic solvent
• a suitable base such as triethylamine in a suitable polar aprotic solvent
• alkylated eg using a suitable alkyl halide and with the aid of
• R 3 of general formula (I) is illustrative but not limiting of OH, OCH 3 , OSO 2 CH 3 , OC (O) CH 3 and OC (O) OCH 3 and R 6 of the general formula (I) is exemplified by, but not limited to, hydrogen.
• Scheme 7 only one of the two possible regioisomers of the compounds of general formula I is shown in Scheme 7 below.
• Citraconic anhydride 2000 mg, 17.84 mmol, 1.0 equiv
• 3-amino-5-tert-butyl-1,2-isoxazole 2501 mg, 17.84 mmol, 1.0 equiv
• Citraconic anhydride 2000 mg, 17.84 mmol, 1.0 equiv.
• 5-amino-3-tert-butyl-1,2-isoxazole 2752 mg, 19.63 mmol, 1.1 equiv
• acetic acid 50 ml
• Citraconic anhydride (519mg, 4.64mmol, 1.1 equiv.) And 3-amino-1,5-diphenyl-1,2-pyrazole (1000mg, 4.21mmol, 1.0 equiv.) Were dissolved in acetonitrile (20mL), eluted with pyridine ( 0.14 ml, 1.69 mmol, 0.4 equiv) and stirred for 14 h under reflux conditions. After cooling to
• Citraconic anhydride 400 mg, 3.57 mmol, 1.0 equiv.
• P-toluenesulfonic acid 92 mg, 0.54 mmol
• 5-amino-3-ethyl-l, 2,4-thiadiazole 461 mg, 3.57 mmol, 1.0 equiv Toluene (12 ml) and stirred for 60 minutes under microwave conditions at a temperature of 85 ° C. After cooling to room temperature, the reaction mixture was washed with water, sat.
• Citraconic anhydride 400 mg, 3.57 mmol, 1.0 equiv
• p-toluenesulfonic acid 92 mg, 0.54 mmol
• 5-amino-3-iso-propyl-l, 2,4-thiadiazole 511 mg, 3.57 mmol, 1.0 equiv
• Preferred compounds of the formula (L I) are the compounds 1.1-1 to 1.1-708, in which Q has the meanings of Table 1 indicated in the respective line.
• the compounds 1.1-1 to 1.1-708 of the Table LI are thus characterized by the meaning of the respective entries no. 1 to 708 defined for Q of Table 1.
• Table 1 :

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Environmental Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Zoology (AREA)
• Wood Science & Technology (AREA)
• Dentistry (AREA)
• Engineering & Computer Science (AREA)
• Plant Pathology (AREA)
• Pest Control & Pesticides (AREA)
• Veterinary Medicine (AREA)
• Animal Behavior & Ethology (AREA)
• Tropical Medicine & Parasitology (AREA)
• Medicinal Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Pharmacology & Pharmacy (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Public Health (AREA)
• Plural Heterocyclic Compounds (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Pyrrole Compounds (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=57614210

Family Applications (1)

Country Status (12)

Families Citing this family (1)

Family Cites Families (54)

• 2017
  • 2017-12-14 EA EA201991548A patent/EA201991548A1/ru unknown
  • 2017-12-14 US US16/471,146 patent/US20200079765A1/en not_active Abandoned
  • 2017-12-14 CA CA3047638A patent/CA3047638A1/en active Pending
  • 2017-12-14 WO PCT/EP2017/082832 patent/WO2018114596A1/de unknown
  • 2017-12-14 BR BR112019012584-1A patent/BR112019012584A2/pt not_active Application Discontinuation
  • 2017-12-14 JP JP2019533561A patent/JP2020502217A/ja active Pending
  • 2017-12-14 CN CN201780085933.7A patent/CN110267950A/zh active Pending
  • 2017-12-14 MX MX2019007374A patent/MX2019007374A/es unknown
  • 2017-12-14 EP EP17823071.0A patent/EP3558975A1/de not_active Withdrawn
  • 2017-12-14 AU AU2017379281A patent/AU2017379281A1/en not_active Abandoned
  • 2017-12-22 AR ARP170103669A patent/AR110446A1/es unknown
  • 2017-12-22 UY UY0001037546A patent/UY37546A/es not_active Application Discontinuation

Also Published As

Similar Documents

Legal Events