AR065471A1 - Proceso para la preparacion de ciertas sulfiliminas sustituidas - Google Patents

Proceso para la preparacion de ciertas sulfiliminas sustituidas

Info

Publication number
AR065471A1
AR065471A1 ARP080100777A ARP080100777A AR065471A1 AR 065471 A1 AR065471 A1 AR 065471A1 AR P080100777 A ARP080100777 A AR P080100777A AR P080100777 A ARP080100777 A AR P080100777A AR 065471 A1 AR065471 A1 AR 065471A1
Authority
AR
Argentina
Prior art keywords
haloalkenyl
haloalkyl
alkynyl
alkenyl
integer
Prior art date
Application number
ARP080100777A
Other languages
English (en)
Original Assignee
Dow Agrosciences Llc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39523499&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR065471(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Dow Agrosciences Llc filed Critical Dow Agrosciences Llc
Publication of AR065471A1 publication Critical patent/AR065471A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/32Sulfur atoms
    • C07D213/34Sulfur atoms to which a second hetero atom is attached

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Se producen cianosulfiliminas sustituidas a partir de los correspondientes sulfuros, por reaccion con cianamida e hipoclorito. Reivindicacion 1: Un proceso para preparar sulfiliminas de la formula (1), en donde Het representa grupo de formulas (2),X representa halogeno, alquilo C1-4, haloalquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquenilo C2-4, alcoxi C1-4, haloalcoxi C1-4, CN, NO2, SOmR6 en donde m es un entero entre 0-2, COOR4 o CONR4R5; Y representa hidrogeno, halogeno, alquilo C1-4, haloalquilo, C1-4, alquenilo C2-4, alquinilo C2-4, haloalquenilo C2-4, alcoxi C1-4, haloalcoxi C1-4, CN, NO2, SOmR1 en donde m es un entero entre 0-2, COOR4, CONR4R5, arilo o heteroarilo; n es un entero entre 0-3; L representa un enlace simple, -CH(CH2)p- en donde R1, S y L tomados juntos representan un anillo de 4, 5 o 6 miembros y p es un entero entre 1-3, -CH(CH2OCH2)- en donde R1, S y L tomados juntos representan un anillo de 6 miembros, o -CH- en donde L, R2 y el carbono comun al queestán conectados tomados juntos representan un anillo de 4, 5 o 6 miembros con hasta, pero no más de 1 heteroátomo; R1 representa alquilo C1-4, haloalquilo C1-4, alquenilo C3-6, alquinilo C3-6, haloalquenilo C3-6, arilalquilo, heteroarilalquilo, o -CH2- en los casos de que R1, S y L tomados juntos representan un anillo de 4, 5 o 6 miembros; R2 y R3 representan independientemente hidrogeno, halogeno, alquilo C1-4, haloalquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquenilo C2-4, alcoxi C1-4, haloalcoxi C1-4, CN, SOmR6 en donde m es un entero entre 0-2, COOR4, CONR4R5, arilalquilo, heteroarilalquilo, o R2 y R3 y el anillo comun al que se unen forma un anillo de 3 a 6 miembros; R4 y R5 representan independientemente hidrogeno, alquiloC1-4, haloalquilo C1-4; alquenilo C3-6, alquinilo C3-6, haloalquenilo C3-6, arilo, heteroarilo, arilalquilo o heteroarilalquilo; y R6 representa alquilo C1-4, haloalquilo C1-4; alquenilo C3-6, alquinilo C3-6, haloalquenilo C3-6, arilalquilo oheteroarilalquilo; que comprende poner en contacto un solfuro de la formula (3) en donde R1, R2, R3, L, Het y n son como se definio con anterioridad con cianamida y solucion de hipoclorito a una temperatura de aproximadamente -40°C a aproximadamente30°C en un solvente orgánico adecuado que es esencialmente inerte en las condiciones de reaccion.
ARP080100777A 2007-02-26 2008-02-25 Proceso para la preparacion de ciertas sulfiliminas sustituidas AR065471A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US90347107P 2007-02-26 2007-02-26

Publications (1)

Publication Number Publication Date
AR065471A1 true AR065471A1 (es) 2009-06-10

Family

ID=39523499

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080100777A AR065471A1 (es) 2007-02-26 2008-02-25 Proceso para la preparacion de ciertas sulfiliminas sustituidas

Country Status (16)

Country Link
US (2) US7868027B2 (es)
EP (1) EP2114886B1 (es)
JP (1) JP5302221B2 (es)
KR (1) KR101437710B1 (es)
CN (1) CN101641331B (es)
AR (1) AR065471A1 (es)
AU (1) AU2008219748B2 (es)
BR (1) BRPI0807702B8 (es)
CA (1) CA2678028C (es)
CL (1) CL2008000564A1 (es)
DK (1) DK2114886T3 (es)
HK (1) HK1141013A1 (es)
IL (1) IL200520A (es)
TW (1) TWI393706B (es)
WO (1) WO2008106006A1 (es)
ZA (1) ZA200905012B (es)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8193222B1 (en) 2007-02-26 2012-06-05 Dow AgroSciences, L.L.C. Process for the preparation of certain substituted sulfilimines
WO2010074747A1 (en) 2008-12-26 2010-07-01 Dow Agrosciences, Llc Stable insecticide compositions and methods for producing same
RU2518251C2 (ru) * 2008-12-26 2014-06-10 ДАУ АГРОСАЙЕНСИЗ, ЭлЭлСи Стабильная пестицидная композиция на основе сульфоксимина и способ борьбы с насекомыми
WO2010075966A1 (de) * 2008-12-29 2010-07-08 Bayer Cropscience Ag Verfahren zur verbesserten nutzung des produktionspotentials genetisch modifizierter pflanzen
EP2223602A1 (de) 2009-02-23 2010-09-01 Bayer CropScience AG Verfahren zur verbesserten Nutzung des Produktionspotentials genetisch modifizierter Pflanzen
EP2223598A1 (de) 2009-02-23 2010-09-01 Bayer CropScience AG Insektizide Zusammensetzungen mit verbesserter Wirkung
US20110306643A1 (en) 2010-04-23 2011-12-15 Bayer Cropscience Ag Triglyceride-containing dormancy sprays
EP2545964A1 (en) 2011-07-13 2013-01-16 Phenex Pharmaceuticals AG Novel FXR (NR1H4) binding and activity modulating compounds
BR102013003576B8 (pt) * 2012-02-16 2022-10-11 Dow Agrosciences Llc Método para produzir n-ciano-s-metil-s-[1-(6-tri-flúormetil-3-piridinil)etil]sulfilimina
US9156784B2 (en) 2012-02-21 2015-10-13 Bayer Intellectual Property Gmbh Herbicidal sulfinimidoyl- and sulfonimidoyl benzoyl derivatives
WO2013124228A1 (de) 2012-02-21 2013-08-29 Bayer Intellectual Property Gmbh Herbizid wirksame 3 - ( sulfin- /sulfonimidoyl) - benzamide
CN104602527B (zh) 2012-06-30 2018-09-25 美国陶氏益农公司 吡啶n-氧化物及其制备方法
KR102089479B1 (ko) 2012-06-30 2020-03-17 다우 아그로사이언시즈 엘엘씨 N-치환된 술폭시민 피리딘 n-옥시드의 제조
CN105324365A (zh) * 2012-12-11 2016-02-10 美国陶氏益农公司 用于制备n-氰基-s-[1-(吡啶-3-基)乙基]-s-甲基硫亚胺的改善方法
EP2873668A1 (en) 2013-11-13 2015-05-20 Syngenta Participations AG. Pesticidally active bicyclic heterocycles with sulphur containing substituents
EP3356343B1 (en) 2015-09-28 2020-03-18 Syngenta Participations AG Pesticidally active heterocyclic derivatives with sulphur containing substituents
ES2921432T3 (es) 2016-06-13 2022-08-25 Gilead Sciences Inc Derivados de azetidina como moduladores de FXR (NR1H4)
CA2968836A1 (en) 2016-06-13 2017-12-13 Gilead Sciences, Inc. Fxr (nr1h4) modulating compounds
TWI735573B (zh) * 2016-06-21 2021-08-11 美商陶氏農業科學公司 生產某些經取代硫亞胺之方法
CA3030946A1 (en) 2016-07-22 2018-01-25 Sumitomo Chemical Company, Limited Herbicide composition including [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate and 2,4-d choline salt and method for controlling weeds
JP7282031B2 (ja) 2016-12-01 2023-05-26 シンジェンタ パーティシペーションズ アーゲー 硫黄含有置換基を有する殺有害生物的に活性な複素環式誘導体
ES2927019T3 (es) 2017-03-28 2022-11-02 Gilead Sciences Inc Combinaciones terapéuticas para el tratamiento de enfermedades hepáticas
JP7309615B2 (ja) 2017-05-02 2023-07-18 シンジェンタ パーティシペーションズ アーゲー 硫黄含有置換基を有する有害生物防除に活性な複素環式誘導体
WO2019219689A1 (en) 2018-05-18 2019-11-21 Syngenta Participations Ag Pesticidally active heterocyclic derivatives with sulfoximine containing substituents
WO2019229089A1 (en) 2018-05-31 2019-12-05 Syngenta Participations Ag Pesticidally active heterocyclic derivatives with sulfur containing substituents
CN112262140B (zh) 2018-06-06 2024-05-28 先正达农作物保护股份公司 具有含亚砜亚胺取代基的杀有害生物活性杂环衍生物
AR115495A1 (es) 2018-06-06 2021-01-27 Syngenta Crop Protection Ag Derivados heterocíclicos con sustituyentes que contienen azufre activos como plaguicidas
TW202035404A (zh) 2018-10-24 2020-10-01 瑞士商先正達農作物保護公司 具有含亞碸亞胺的取代基之殺有害生物活性雜環衍生物
DK3911647T3 (da) 2019-01-15 2024-02-26 Gilead Sciences Inc Isoxazol-forbindelse som FXR-agonist og farmaceutiske sammensætninger, der omfatter en sådan
CN113439078B (zh) 2019-02-19 2024-04-23 吉利德科学公司 Fxr激动剂的固体形式
MX2023006990A (es) 2020-12-14 2023-06-26 Basf Se Plaguicidas de sulfoximina.
CA3221102A1 (en) 2021-06-02 2022-12-08 Michel Muehlebach Pesticidally active heterocyclic derivatives with sulfoximine containing substituents

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7678920B2 (en) 2004-04-08 2010-03-16 Dow Agrosciences Llc Insecticidal N-substituted sulfoximines
TWI398433B (zh) * 2006-02-10 2013-06-11 Dow Agrosciences Llc 殺蟲性之n-取代(6-鹵烷基吡啶-3-基)烷基磺醯亞胺

Also Published As

Publication number Publication date
BRPI0807702A2 (pt) 2014-05-27
JP5302221B2 (ja) 2013-10-02
WO2008106006A1 (en) 2008-09-04
DK2114886T3 (da) 2014-06-30
IL200520A0 (en) 2010-04-29
AU2008219748A1 (en) 2008-09-04
EP2114886B1 (en) 2014-03-26
TW200844097A (en) 2008-11-16
CL2008000564A1 (es) 2008-08-29
KR20090113870A (ko) 2009-11-02
AU2008219748B2 (en) 2012-05-03
CA2678028A1 (en) 2008-09-04
EP2114886A1 (en) 2009-11-11
US7868027B2 (en) 2011-01-11
TWI393706B (zh) 2013-04-21
IL200520A (en) 2014-02-27
CA2678028C (en) 2015-02-03
HK1141013A1 (en) 2010-10-29
KR101437710B1 (ko) 2014-09-03
US20080207910A1 (en) 2008-08-28
CN101641331A (zh) 2010-02-03
ZA200905012B (en) 2010-10-27
CN101641331B (zh) 2012-06-27
US20110077409A1 (en) 2011-03-31
BRPI0807702B1 (pt) 2016-11-01
BRPI0807702B8 (pt) 2022-06-28
JP2010519296A (ja) 2010-06-03

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