compostos substituídos por halogênio, uso dos mesmos, processo para o combate de parasitos, processo para a preparação de reparados para proteger plantas e composições farmacêuticas

Aromatic compounds (I) are new. Aromatic compounds of formula (I) are new. R 1> : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; A 1> : CR 2> or N; A 2> : CR 3> or N; A 3> : CR 4> or N; A 4> : CR 5> or N; R 2>-R 5> : e.g. H, halo, CN or NO 2; L : bivalent...

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Hauptverfasser: Michael Maue, Markus Heil, Martin Adamczewski, Tobias Kapferer, Mark Wilhelm Drewes, Ulrich Göegens, Friedrich August Mühlthau, Peter Jeschke, Arnd Voerste, Klaus Raming, Alexander Sudau, Ulrich Ebbinghaus-Kintscher, Angela Becker, Bernd-Wieland Krüger, Wolfgang Giencke, Eva Maria Franken, Isdabelle Adelt
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creator Michael Maue
Markus Heil
Martin Adamczewski
Tobias Kapferer
Mark Wilhelm Drewes
Ulrich Göegens
Friedrich August Mühlthau
Peter Jeschke
Arnd Voerste
Klaus Raming
Alexander Sudau
Ulrich Ebbinghaus-Kintscher
Angela Becker
Bernd-Wieland Krüger
Wolfgang Giencke
Eva Maria Franken
Isdabelle Adelt
description Aromatic compounds (I) are new. Aromatic compounds of formula (I) are new. R 1> : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; A 1> : CR 2> or N; A 2> : CR 3> or N; A 3> : CR 4> or N; A 4> : CR 5> or N; R 2>-R 5> : e.g. H, halo, CN or NO 2; L : bivalent group, e.g. NHC(W 1>); Q : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; U 1> : C(W 1>), SO or SO 2; W 1> : O or S; T : optionally saturated 5- or 6-membered (hetero)cycle (optionally substituted); and m : 0 or 1. With proviso. Independent claims are included for: (1) 2H-pyrazole-3-carboxylic acid compound of formula (V6); and (2) preparation of a plant protectant comprising (I), diluents and/or surface active substance. Z1a = 1,2,2,2-tetrafluoroethyl, 1-chloro-1,2,2,2-tetrafluoroethyl, 2,2,2-trichloroethyl, 2-chloro-2,2-difluoroethyl, pentafluoroethyl, 1,1-difluoroethyl, pentafluoro-tert-butyl, heptafluoro-n-propyl, heptafluoro-isopropyl, nonafluoro-n-butyl, trifluoromethoxy-1,1,2,2-tetrafluoroethoxy-difluoromethyl, CF 3O, CF 2HO, chlorodifluoromethyl, dichlorofluoromethyl, difluoromethyl, 2,2,2-trifluoroethyl or 2,2-difluoro-1-methylcyclopropyl; Z2b = F, Cl, Br, I, Cn, niro, methyl, ethyl, (iso)propyl, cyclopropyl, CF3, CF2CF3, heptafluoropropyl, ethenyl, propenyl, ethynyl, 1-propynyl, 1-butynyl or 4-fluorophenyl; Z3b = methyl, ethyl (iso)propyl, (iso)buyl, sec-butyl, t-butyl, 1-fluoro-1-methylethyl, 1-fluoroethyl, 2-ethoxyethyl, 2-methoxyethyl, cyclobutyl or cyclopentyl. [Image] ACTIVITY : Insecticide; Arachnicide; Nematocide; Arthropodicide; Acaricide; Anthelmintic; Protozoacide; Fungicide; Antibacterial; Virucide. MECHANISM OF ACTION : None given.
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Aromatic compounds of formula (I) are new. R 1&gt; : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; A 1&gt; : CR 2&gt; or N; A 2&gt; : CR 3&gt; or N; A 3&gt; : CR 4&gt; or N; A 4&gt; : CR 5&gt; or N; R 2&gt;-R 5&gt; : e.g. H, halo, CN or NO 2; L : bivalent group, e.g. NHC(W 1&gt;); Q : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; U 1&gt; : C(W 1&gt;), SO or SO 2; W 1&gt; : O or S; T : optionally saturated 5- or 6-membered (hetero)cycle (optionally substituted); and m : 0 or 1. With proviso. Independent claims are included for: (1) 2H-pyrazole-3-carboxylic acid compound of formula (V6); and (2) preparation of a plant protectant comprising (I), diluents and/or surface active substance. Z1a = 1,2,2,2-tetrafluoroethyl, 1-chloro-1,2,2,2-tetrafluoroethyl, 2,2,2-trichloroethyl, 2-chloro-2,2-difluoroethyl, pentafluoroethyl, 1,1-difluoroethyl, pentafluoro-tert-butyl, heptafluoro-n-propyl, heptafluoro-isopropyl, nonafluoro-n-butyl, trifluoromethoxy-1,1,2,2-tetrafluoroethoxy-difluoromethyl, CF 3O, CF 2HO, chlorodifluoromethyl, dichlorofluoromethyl, difluoromethyl, 2,2,2-trifluoroethyl or 2,2-difluoro-1-methylcyclopropyl; Z2b = F, Cl, Br, I, Cn, niro, methyl, ethyl, (iso)propyl, cyclopropyl, CF3, CF2CF3, heptafluoropropyl, ethenyl, propenyl, ethynyl, 1-propynyl, 1-butynyl or 4-fluorophenyl; Z3b = methyl, ethyl (iso)propyl, (iso)buyl, sec-butyl, t-butyl, 1-fluoro-1-methylethyl, 1-fluoroethyl, 2-ethoxyethyl, 2-methoxyethyl, cyclobutyl or cyclopentyl. [Image] ACTIVITY : Insecticide; Arachnicide; Nematocide; Arthropodicide; Acaricide; Anthelmintic; Protozoacide; Fungicide; Antibacterial; Virucide. MECHANISM OF ACTION : None given.</description><language>por</language><subject>AGRICULTURE ; ANIMAL HUSBANDRY ; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES ; CHEMISTRY ; FISHING ; FORESTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HUNTING ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PEST REPELLANTS OR ATTRACTANTS ; PLANT GROWTH REGULATORS ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS ; TRAPPING</subject><creationdate>2018</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20180424&amp;DB=EPODOC&amp;CC=BR&amp;NR=PI0921277A2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20180424&amp;DB=EPODOC&amp;CC=BR&amp;NR=PI0921277A2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Michael Maue</creatorcontrib><creatorcontrib>Markus Heil</creatorcontrib><creatorcontrib>Martin Adamczewski</creatorcontrib><creatorcontrib>Tobias Kapferer</creatorcontrib><creatorcontrib>Mark Wilhelm Drewes</creatorcontrib><creatorcontrib>Ulrich Göegens</creatorcontrib><creatorcontrib>Friedrich August Mühlthau</creatorcontrib><creatorcontrib>Peter Jeschke</creatorcontrib><creatorcontrib>Arnd Voerste</creatorcontrib><creatorcontrib>Klaus Raming</creatorcontrib><creatorcontrib>Alexander Sudau</creatorcontrib><creatorcontrib>Ulrich Ebbinghaus-Kintscher</creatorcontrib><creatorcontrib>Angela Becker</creatorcontrib><creatorcontrib>Bernd-Wieland Krüger</creatorcontrib><creatorcontrib>Wolfgang Giencke</creatorcontrib><creatorcontrib>Eva Maria Franken</creatorcontrib><creatorcontrib>Isdabelle Adelt</creatorcontrib><title>compostos substituídos por halogênio, uso dos mesmos, processo para o combate de parasitos, processo para a preparação de reparados para proteger plantas e composições farmacêuticas</title><description>Aromatic compounds (I) are new. Aromatic compounds of formula (I) are new. R 1&gt; : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; A 1&gt; : CR 2&gt; or N; A 2&gt; : CR 3&gt; or N; A 3&gt; : CR 4&gt; or N; A 4&gt; : CR 5&gt; or N; R 2&gt;-R 5&gt; : e.g. H, halo, CN or NO 2; L : bivalent group, e.g. NHC(W 1&gt;); Q : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; U 1&gt; : C(W 1&gt;), SO or SO 2; W 1&gt; : O or S; T : optionally saturated 5- or 6-membered (hetero)cycle (optionally substituted); and m : 0 or 1. With proviso. Independent claims are included for: (1) 2H-pyrazole-3-carboxylic acid compound of formula (V6); and (2) preparation of a plant protectant comprising (I), diluents and/or surface active substance. Z1a = 1,2,2,2-tetrafluoroethyl, 1-chloro-1,2,2,2-tetrafluoroethyl, 2,2,2-trichloroethyl, 2-chloro-2,2-difluoroethyl, pentafluoroethyl, 1,1-difluoroethyl, pentafluoro-tert-butyl, heptafluoro-n-propyl, heptafluoro-isopropyl, nonafluoro-n-butyl, trifluoromethoxy-1,1,2,2-tetrafluoroethoxy-difluoromethyl, CF 3O, CF 2HO, chlorodifluoromethyl, dichlorofluoromethyl, difluoromethyl, 2,2,2-trifluoroethyl or 2,2-difluoro-1-methylcyclopropyl; Z2b = F, Cl, Br, I, Cn, niro, methyl, ethyl, (iso)propyl, cyclopropyl, CF3, CF2CF3, heptafluoropropyl, ethenyl, propenyl, ethynyl, 1-propynyl, 1-butynyl or 4-fluorophenyl; Z3b = methyl, ethyl (iso)propyl, (iso)buyl, sec-butyl, t-butyl, 1-fluoro-1-methylethyl, 1-fluoroethyl, 2-ethoxyethyl, 2-methoxyethyl, cyclobutyl or cyclopentyl. [Image] ACTIVITY : Insecticide; Arachnicide; Nematocide; Arthropodicide; Acaricide; Anthelmintic; Protozoacide; Fungicide; Antibacterial; Virucide. MECHANISM OF ACTION : None given.</description><subject>AGRICULTURE</subject><subject>ANIMAL HUSBANDRY</subject><subject>BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES</subject><subject>CHEMISTRY</subject><subject>FISHING</subject><subject>FORESTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HUNTING</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEST REPELLANTS OR ATTRACTANTS</subject><subject>PLANT GROWTH REGULATORS</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><subject>TRAPPING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2018</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjr8OAUEQh69RCN5hoibhFKJECJ2IXsaaY5O7m83O3BMpJBKlTrcvZg-dRjXz_fLNn2byNFw4FmUBqQ6iVqtwP0Zy7OGMOZ_CrbTcg0oY6rwgKVh64Dwbkhg69AgMcc8BleBI70Ss_loYmeouXMOFa_WD73u1EHWlE3lwOZaKAgSf_2yceJBAhr5AE26VWoPSThoZ5kKdb20l3eViN1_1yfGexKGhknQ_227Wg0k6TMfjaTr6S3oBZsJl9w</recordid><startdate>20180424</startdate><enddate>20180424</enddate><creator>Michael Maue</creator><creator>Markus Heil</creator><creator>Martin Adamczewski</creator><creator>Tobias Kapferer</creator><creator>Mark Wilhelm Drewes</creator><creator>Ulrich Göegens</creator><creator>Friedrich August Mühlthau</creator><creator>Peter Jeschke</creator><creator>Arnd Voerste</creator><creator>Klaus Raming</creator><creator>Alexander Sudau</creator><creator>Ulrich Ebbinghaus-Kintscher</creator><creator>Angela Becker</creator><creator>Bernd-Wieland Krüger</creator><creator>Wolfgang Giencke</creator><creator>Eva Maria Franken</creator><creator>Isdabelle Adelt</creator><scope>EVB</scope></search><sort><creationdate>20180424</creationdate><title>compostos substituídos por halogênio, uso dos mesmos, processo para o combate de parasitos, processo para a preparação de reparados para proteger plantas e composições farmacêuticas</title><author>Michael Maue ; Markus Heil ; Martin Adamczewski ; Tobias Kapferer ; Mark Wilhelm Drewes ; Ulrich Göegens ; Friedrich August Mühlthau ; Peter Jeschke ; Arnd Voerste ; Klaus Raming ; Alexander Sudau ; Ulrich Ebbinghaus-Kintscher ; Angela Becker ; Bernd-Wieland Krüger ; Wolfgang Giencke ; Eva Maria Franken ; Isdabelle Adelt</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_BRPI0921277A23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>por</language><creationdate>2018</creationdate><topic>AGRICULTURE</topic><topic>ANIMAL HUSBANDRY</topic><topic>BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES</topic><topic>CHEMISTRY</topic><topic>FISHING</topic><topic>FORESTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HUNTING</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEST REPELLANTS OR ATTRACTANTS</topic><topic>PLANT GROWTH REGULATORS</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><topic>TRAPPING</topic><toplevel>online_resources</toplevel><creatorcontrib>Michael Maue</creatorcontrib><creatorcontrib>Markus Heil</creatorcontrib><creatorcontrib>Martin Adamczewski</creatorcontrib><creatorcontrib>Tobias Kapferer</creatorcontrib><creatorcontrib>Mark Wilhelm Drewes</creatorcontrib><creatorcontrib>Ulrich Göegens</creatorcontrib><creatorcontrib>Friedrich August Mühlthau</creatorcontrib><creatorcontrib>Peter Jeschke</creatorcontrib><creatorcontrib>Arnd Voerste</creatorcontrib><creatorcontrib>Klaus Raming</creatorcontrib><creatorcontrib>Alexander Sudau</creatorcontrib><creatorcontrib>Ulrich Ebbinghaus-Kintscher</creatorcontrib><creatorcontrib>Angela Becker</creatorcontrib><creatorcontrib>Bernd-Wieland Krüger</creatorcontrib><creatorcontrib>Wolfgang Giencke</creatorcontrib><creatorcontrib>Eva Maria Franken</creatorcontrib><creatorcontrib>Isdabelle Adelt</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Michael Maue</au><au>Markus Heil</au><au>Martin Adamczewski</au><au>Tobias Kapferer</au><au>Mark Wilhelm Drewes</au><au>Ulrich Göegens</au><au>Friedrich August Mühlthau</au><au>Peter Jeschke</au><au>Arnd Voerste</au><au>Klaus Raming</au><au>Alexander Sudau</au><au>Ulrich Ebbinghaus-Kintscher</au><au>Angela Becker</au><au>Bernd-Wieland Krüger</au><au>Wolfgang Giencke</au><au>Eva Maria Franken</au><au>Isdabelle Adelt</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>compostos substituídos por halogênio, uso dos mesmos, processo para o combate de parasitos, processo para a preparação de reparados para proteger plantas e composições farmacêuticas</title><date>2018-04-24</date><risdate>2018</risdate><abstract>Aromatic compounds (I) are new. Aromatic compounds of formula (I) are new. R 1&gt; : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; A 1&gt; : CR 2&gt; or N; A 2&gt; : CR 3&gt; or N; A 3&gt; : CR 4&gt; or N; A 4&gt; : CR 5&gt; or N; R 2&gt;-R 5&gt; : e.g. H, halo, CN or NO 2; L : bivalent group, e.g. NHC(W 1&gt;); Q : e.g. H, optionally substituted 1-6C-alkyl or 2-6C-alkenyl; U 1&gt; : C(W 1&gt;), SO or SO 2; W 1&gt; : O or S; T : optionally saturated 5- or 6-membered (hetero)cycle (optionally substituted); and m : 0 or 1. With proviso. Independent claims are included for: (1) 2H-pyrazole-3-carboxylic acid compound of formula (V6); and (2) preparation of a plant protectant comprising (I), diluents and/or surface active substance. Z1a = 1,2,2,2-tetrafluoroethyl, 1-chloro-1,2,2,2-tetrafluoroethyl, 2,2,2-trichloroethyl, 2-chloro-2,2-difluoroethyl, pentafluoroethyl, 1,1-difluoroethyl, pentafluoro-tert-butyl, heptafluoro-n-propyl, heptafluoro-isopropyl, nonafluoro-n-butyl, trifluoromethoxy-1,1,2,2-tetrafluoroethoxy-difluoromethyl, CF 3O, CF 2HO, chlorodifluoromethyl, dichlorofluoromethyl, difluoromethyl, 2,2,2-trifluoroethyl or 2,2-difluoro-1-methylcyclopropyl; Z2b = F, Cl, Br, I, Cn, niro, methyl, ethyl, (iso)propyl, cyclopropyl, CF3, CF2CF3, heptafluoropropyl, ethenyl, propenyl, ethynyl, 1-propynyl, 1-butynyl or 4-fluorophenyl; Z3b = methyl, ethyl (iso)propyl, (iso)buyl, sec-butyl, t-butyl, 1-fluoro-1-methylethyl, 1-fluoroethyl, 2-ethoxyethyl, 2-methoxyethyl, cyclobutyl or cyclopentyl. [Image] ACTIVITY : Insecticide; Arachnicide; Nematocide; Arthropodicide; Acaricide; Anthelmintic; Protozoacide; Fungicide; Antibacterial; Virucide. MECHANISM OF ACTION : None given.</abstract><oa>free_for_read</oa></addata></record>
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subjects AGRICULTURE
ANIMAL HUSBANDRY
BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES
CHEMISTRY
FISHING
FORESTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HUNTING
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PEST REPELLANTS OR ATTRACTANTS
PLANT GROWTH REGULATORS
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
TRAPPING
title compostos substituídos por halogênio, uso dos mesmos, processo para o combate de parasitos, processo para a preparação de reparados para proteger plantas e composições farmacêuticas
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