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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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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fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_BRPI0921277A2</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>BRPI0921277A2</sourcerecordid><originalsourceid>FETCH-epo_espacenet_BRPI0921277A23</originalsourceid><addsrcrecordid>eNqNjr8OAUEQh69RCN5hoibhFKJECJ2IXsaaY5O7m83O3BMpJBKlTrcvZg-dRjXz_fLNn2byNFw4FmUBqQ6iVqtwP0Zy7OGMOZ_CrbTcg0oY6rwgKVh64Dwbkhg69AgMcc8BleBI70Ss_loYmeouXMOFa_WD73u1EHWlE3lwOZaKAgSf_2yceJBAhr5AE26VWoPSThoZ5kKdb20l3eViN1_1yfGexKGhknQ_227Wg0k6TMfjaTr6S3oBZsJl9w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><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><source>esp@cenet</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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&date=20180424&DB=EPODOC&CC=BR&NR=PI0921277A2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20180424&DB=EPODOC&CC=BR&NR=PI0921277A2$$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> : 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.</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> : 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.</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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