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AR050516A1 - Bifeniltiazolcarboxamidas. composiciones antimicrobianas - Google Patents

Bifeniltiazolcarboxamidas. composiciones antimicrobianas

Info

Publication number
AR050516A1
AR050516A1 ARP050103215A ARP050103215A AR050516A1 AR 050516 A1 AR050516 A1 AR 050516A1 AR P050103215 A ARP050103215 A AR P050103215A AR P050103215 A ARP050103215 A AR P050103215A AR 050516 A1 AR050516 A1 AR 050516A1
Authority
AR
Argentina
Prior art keywords
alkyl
carbonyl
halogen
alkoxy
halogenoalkyl
Prior art date
Application number
ARP050103215A
Other languages
English (en)
Original Assignee
Bayer Cropscience Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag
Publication of AR050516A1 publication Critical patent/AR050516A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, 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
    • A01N43/74Biocides, 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
    • A01N43/781,3-Thiazoles; Hydrogenated 1,3-thiazoles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Environmental Sciences (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Pest Control & Pesticides (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Composiciones antimicrobianas y compuestos intermediarios. Reivindicacion 1: Bifeniltiazolcarboxamidas de la formula (1), en la que: R1 significa hidrogeno, halogeno, amino, alquilamino C1-4, di-(alquilo C1-4)amino, ciano, alquilo C1-4 o halogenoalquilo C1-4 con 1 hasta 5 átomos de halogeno; R2 significa halogeno, alquilo C1-4 o halogenoalquilo C1-4 con 1 hasta 5 átomos de halogeno; R3 significa hidrogeno, alquilo C1-8, alquilsulfinilo C1-6, alquilsulfonilo C1-6, alcoxiC1-4- alquiloC1-4, cicloalquilo C3-8; halogenoalquilo C1-6, halogenoalquiltio C1-4, halogenoalquilsulfinilo C1-4, halogenoalquilsulfonilo C1-4, halogeno-alcoxiC1-4-alquiloC1-4, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; formilo, formil-alquiloC1-3, (alquilo C1-3)carbonil-alquiloC1-3, (alcoxi C1-3)carbonil-alquiloC1-3; halogeno-(alquilo C1-3)carbonil-alquiloC1-3, halogeno-(alcoxi C1-3)carbonil-alquiloC1-3 con, respectivamente, 1 hasta 13 átomos de fluor, de cloro y/o de bromo; (alquilo C1-8)carbonilo, (alcoxi C1-8)carbonilo, (alcoxiC1-4-alquiloC1-4)carbonilo, (cicloalquilo C3-8)carbonilo; (halogenoalquilo C1-6)carbonilo, (halogenoalcoxi C1-6)carbonilo, (halogeno-alcoxiC1-4-alquiloC1- 4)carbonilo, (halogenocicloalquilo C3-8)carbonilo con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; o -C(=O)C(=O)R6, -CONR7R8 o -CH2NR9R10; R4 significa halogeno, alquilo C1-4, alcoxi C1-4, alquiltio C1-4 o halogenoalquilo C1-4 con 1 hasta 9 átomos de fluor, de cloro y/o de bromo; m significa 1 o 2, pudiendo ser iguales o diferentes los restos R4, cuando m signifique 2; R5 significa halogeno, ciano, nitro, amino, hidroxi, formilo, carboxi, carbamoilo, tiocarbamoilo, alquilo C1-8, alquenilo C2-6, alcoxi C1-8, alqueniloxi C2-6, alquiltio C1-8, alquilsulfinilo C1-8, alquilsulfonilo C1-8, hidroxialquilo C1-8, oxoalquilo C1-8, alcoxialquilo C1-8, alquiltioalquilo C1-8, dialcoxialquilo C1-8, alquilamino C1-6, di(alquilo C1-6)amino, (alquilo C1-6)carbonilo, (alquilo C1-6)carboniloxi, (alcoxi C1-6)carbonilo, (alquilo C1-6)aminocarbonilo, di(alquilo C1-6)aminocarbonilo, (alquilo C1-6)carbonilamino, (alquilo C1-6)carbonil(alquilo C1-6)amino, (alquenilo C2- 6)carbonilo, (alquinilo C2-6)carbonilo, cicloalquilo C3-6, cicloalquiloxi C3-6, o significa halogenoalquilo C1-6, halogenoalcoxi C1-6, halogenoalquiltio C1-6, halogenoalquilsulfinilo C1-6 o halogenoalquilsulfonilo C1-6 con, respectivamente, 1 hasta 13 átomos de halogeno, halogenoalquenilo C2-6, halogenoalqueniloxi C2-6 con, respectivamente, 1 hasta 11 átomos de halogeno iguales o diferentes; R6 significa hidrogeno, alquilo C1-8, alcoxi C1-8, alcoxiC1-4-alquiloC1-4, cicloalquilo C3-8; halogenoalquilo C1-6, halogenoalcoxi C1-6, halogeno-alcoxiC1-4-alquiloC1-4, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; R7 y R8 significan, independientemente entre sí, hidrogeno, alquilo C1-8, alcoxiC1-4-alquiloC1-4, cicloalquilo C3-8; halogenoalquilo C1-8, halogeno-alcoxiC1-4-alquiloC1-4, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; R7 y R8 además significan, junto con el átomo de nitrogeno, con el que están enlazados, un heterociclo saturado, con hasta 5 hasta 8 átomos en el anillo, sustituido, en caso dado, una o varias veces, de forma igual o de formas diferentes por halogeno o por alquilo C1-4, pudiendo contener el heterociclo 1 o 2 heteroátomos más, no contiguos, de la serie formada por oxígeno, azufre o NR11; R9 y R10 significan, independientemente entre sí, hidrogeno, alquilo C1-8, cicloalquilo C3-8; halogenoalquilo C1-8, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; R9 y R10 además significan, junto con el átomo de nitrogeno, con el que están enlazados, un heterociclo saturado, con 5 hasta 8 átomos en el anillo, sustituido, en caso dado, una o varias veces, de forma igual o de formas diferentes por halogeno o por alquilo C1-4, pudiendo contener el heterociclo 1 o 2 heteroátomos más, no contiguos, de la serie formada por oxígeno, azufre o NR11; R11 significa hidrogeno o alquilo C1-6, quedando excluidos los compuestos de la formula (1), en la que: R1 significa hidrogeno o metilo; R2 significa cloro, metilo, difluormetilo o trifluormetilo; R5 significa halogeno, alquilo C1-4, trifluormetilo, alcoxi C1-4 o alquiltio C1-4, cuando R3 signifique hidrogeno y R4 signifique fluor y m signifique 1.
ARP050103215A 2004-08-27 2005-08-02 Bifeniltiazolcarboxamidas. composiciones antimicrobianas AR050516A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102004041532A DE102004041532A1 (de) 2004-08-27 2004-08-27 Biphenylthiazolcarboxamide

Publications (1)

Publication Number Publication Date
AR050516A1 true AR050516A1 (es) 2006-11-01

Family

ID=35745600

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050103215A AR050516A1 (es) 2004-08-27 2005-08-02 Bifeniltiazolcarboxamidas. composiciones antimicrobianas

Country Status (12)

Country Link
US (1) US20090105316A1 (es)
EP (1) EP1786795A2 (es)
JP (1) JP2008510746A (es)
KR (1) KR20070050958A (es)
CN (1) CN101044128B (es)
AR (1) AR050516A1 (es)
BR (1) BRPI0514439A (es)
CA (1) CA2577997A1 (es)
CR (1) CR8879A (es)
DE (1) DE102004041532A1 (es)
MX (1) MX2007002243A (es)
WO (1) WO2006024389A2 (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10246959A1 (de) * 2002-10-09 2004-04-22 Bayer Cropscience Ag Thiazolylbiphenylamide
DE102004005786A1 (de) * 2004-02-06 2005-08-25 Bayer Cropscience Ag Haloalkylcarboxamide
DE102004041530A1 (de) * 2004-08-27 2006-03-02 Bayer Cropscience Ag Biphenylthiazolcarboxamide
DE102005022147A1 (de) * 2005-04-28 2006-11-02 Bayer Cropscience Ag Wirkstoffkombinationen
CN101484009B (zh) * 2006-05-03 2013-08-07 巴斯夫欧洲公司 芳基甲酸联苯基酰胺在种子处理中的用途
JO3598B1 (ar) 2006-10-10 2020-07-05 Infinity Discovery Inc الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني
AU2009233711B2 (en) 2008-04-09 2015-02-12 Infinity Pharmaceuticals, Inc Inhibitors of fatty acid amide hydrolase
BRPI0911898A2 (pt) 2008-05-02 2015-10-13 Basf Se processo para preparar compostos, e, composto.
AR074623A1 (es) 2008-05-02 2011-02-02 Basf Se Procedimiento para la preparacion de esteres de acido 2-(aminometiliden)-3-oxobutirico, sustituidos por halogeno
US8598222B2 (en) 2008-05-05 2013-12-03 Basf Se Method for preparing 1,3,4-substituted pyrazol compounds
WO2010009990A1 (en) * 2008-07-21 2010-01-28 Basf Se Process for preparing 1,3-disubstituted pyrazolecarboxylic esters
JP2012523425A (ja) 2009-04-07 2012-10-04 インフイニトイ プハルマセウトイカルス インコーポレイテッド 脂肪酸アミドヒドロラーゼの阻害薬
ES2493916T3 (es) 2009-04-07 2014-09-12 Infinity Pharmaceuticals, Inc. Inhibidores de hidrolasa de amida de ácidos grasos
CN102596911B (zh) 2009-11-05 2015-04-08 巴斯夫欧洲公司 制备缩醛胺的方法及其在制备1,3-二取代的吡唑化合物中的用途
CN102596912B (zh) 2009-11-05 2015-08-12 巴斯夫欧洲公司 制备1,3-二取代吡唑化合物的方法
BR112012019120A2 (pt) 2010-02-03 2016-06-28 Infinity Pharmaceuticais Inc forma sólida, composição farmacêutica, método de preparação do composto 1, método de tratamento de uma condição mediada por faah
CN102344578A (zh) * 2011-09-09 2012-02-08 深圳市金钒能源科技有限公司 一种离子膜的生产方法
EP3178813A1 (en) 2015-12-09 2017-06-14 Basf Se Method for preparing halogenated 3-oxocarboxylates carrying a 2-alkoxymethylidene or a 2-dialkylaminomethylidene group

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5045554A (en) * 1988-11-29 1991-09-03 Monsanto Company Substituted thiazoles and their use as fungicides
AU6049590A (en) * 1989-07-25 1991-02-22 Monsanto Company Substituted carboxanilidothiazoles and their use as fungicides
DE19531813A1 (de) * 1995-08-30 1997-03-06 Basf Ag Bisphenylamide
DE60018253T2 (de) * 1999-12-16 2005-07-21 Dow Agrosciences Llc, Indianapolis Die Verwendung von 5-Carboxanilido-2,4-bis-trifluoromethylthiazole gegen Reisbräune
AU7200300A (en) * 1999-12-16 2001-06-21 Rohm And Haas Company 5-carboxanilido-haloalkylthiazoles as antimicrobial and marine antifouling agents
GB0101996D0 (en) * 2001-01-25 2001-03-14 Syngenta Participations Ag Organtic compounds
DE10204391A1 (de) * 2002-02-04 2003-08-14 Bayer Cropscience Ag Difluormethylthiazolylcarboxanilide
DE10246959A1 (de) * 2002-10-09 2004-04-22 Bayer Cropscience Ag Thiazolylbiphenylamide
DE10347090A1 (de) * 2003-10-10 2005-05-04 Bayer Cropscience Ag Synergistische fungizide Wirkstoffkombinationen
DE10349501A1 (de) * 2003-10-23 2005-05-25 Bayer Cropscience Ag Synergistische fungizide Wirkstoffkombinationen
DE102004041530A1 (de) * 2004-08-27 2006-03-02 Bayer Cropscience Ag Biphenylthiazolcarboxamide
DE102005060462A1 (de) * 2005-12-17 2007-06-28 Bayer Cropscience Ag Biphenylcarboxamide

Also Published As

Publication number Publication date
CN101044128B (zh) 2012-04-18
MX2007002243A (es) 2007-04-20
WO2006024389A3 (de) 2006-05-18
WO2006024389A2 (de) 2006-03-09
CR8879A (es) 2007-08-28
KR20070050958A (ko) 2007-05-16
US20090105316A1 (en) 2009-04-23
JP2008510746A (ja) 2008-04-10
EP1786795A2 (de) 2007-05-23
DE102004041532A1 (de) 2006-03-02
BRPI0514439A (pt) 2008-06-10
CN101044128A (zh) 2007-09-26
CA2577997A1 (en) 2006-03-09

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