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AR100312A1 - Compuestos de diaminotriazina - Google Patents

Compuestos de diaminotriazina

Info

Publication number
AR100312A1
AR100312A1 ARP150101094A ARP150101094A AR100312A1 AR 100312 A1 AR100312 A1 AR 100312A1 AR P150101094 A ARP150101094 A AR P150101094A AR P150101094 A ARP150101094 A AR P150101094A AR 100312 A1 AR100312 A1 AR 100312A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkoxy
cycloalkyl
carbonyl
group
Prior art date
Application number
ARP150101094A
Other languages
English (en)
Original Assignee
Basf Se
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 Basf Se filed Critical Basf Se
Publication of AR100312A1 publication Critical patent/AR100312A1/es

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
    • 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
    • A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
    • A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40—Nitrogen atoms
    • C07D251/48—Two nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Reivindicación 1: Un compuesto de diaminotriazina de la fórmula (1) en donde q es 0, 1, 2 ó 3, Rᵃ se selecciona del grupo que consiste en C₁₋₆-haloalcoxi, C₁₋₆-haloalquiltio, (C₁₋₆-haloalquil)sulfinilo, (C₁₋₆-haloalquil)-carbonilo, (C₁₋₆-haloalquil)sulfonilo, C₂₋₆-alqueniloxi, C₂₋₆-haloalqueniloxi, C₂₋₆-alquiniloxi, C₂₋₆-haloalquiniloxi, (C₁₋₆-haloalcoxi)-C₁₋₆ alcoxi, (C₁₋₆-alquil)-carboniloxi, (C₁₋₆-haloalquil)-carboniloxi, C₃₋₆-cicloalcoxi, C₃₋₆-halocicloalcoxi, (C₃₋₆-cicloalquil)-C₁₋₄-alcoxi, (C₃₋₆-halocicloalquil)-C₁₋₄-alcoxi, (C₃₋₆-cicloalquil)-C₁₋₄-alquilo, (C₃₋₆-halocicloalquil)-C₁₋₄-alquilo, (C₃₋₆-cicloalcoxi)-C₁₋₄-alquilo, (C₃₋₆-halocicloalcoxi)-C₁₋₄-alquilo, (C₃₋₆-cicloalquil)-carboniloxi, (C₁₋₆-alcoxi)-C₁₋₆-alcoxi; Rᵇ se selecciona del grupo que consiste en halógeno, OH, CN, amino, NO₂, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi, C₂₋₆-alqueniloxi, C₂₋₆-alquiniloxi, (C₁₋₆-alcoxi)-C₁₋₆-alquilo, (C₁₋₆-alcoxi)-C₁₋₆-alcoxi, (C₁₋₆-alcoxi)-C₂₋₆-alquenilo, (C₁₋₆-alcoxi)-C₂₋₆-alquinilo, C₁₋₆-alquiltio, (C₁₋₆-alquil)sulfinilo, (C₁₋₆-alquil)sulfonilo, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, (C₁₋₆-alquil)-carbonilo, (C₁₋₆-alcoxi)-carbonilo, (C₁₋₆-alquil)-carboniloxi, C₃₋₆-cicloalquilo, C₃₋₆-cicloalcoxi, (C₃₋₆-cicloalquil)-C₁₋₄-alquilo, (C₃₋₆-cicloalquil)-C₁₋₄-alcoxi, (C₃₋₆-cicloalcoxi)-C₁₋₄-alquilo, (C₃₋₆-cicloalquil)-carboniloxi, en donde las partes alifáticas y cicloalifáticas de los 24 radicales antes mencionados son no sustituidas, parcial o totalmente halogenadas, y en donde las partes cicloalifáticas de los últimos 6 radicales mencionados pueden tener 1, 2, 3, 4, 5 ó 6 grupos metilo, cuando q = 2 ó 3, es posible que los Rᵇ sean idénticos o diferentes; R¹ se selecciona del grupo que consiste en H, OH, S(O)₂NH₂, CN, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, (C₃₋₆-cicloalquil)-C₁₋₄-alquilo, C₁₋₆-alcoxi, (C₁₋₆-alcoxi)-C₁₋₆-alquilo, (C₁₋₆-alquil)carbonilo, (C₃₋₆-cicloalquil)carbonilo, (C₁₋₆-alcoxi)carbonilo, (C₁₋₆-alquil)sulfonilo, (C₁₋₆-alquilamino)carbonilo, di(C₁₋₆-alquil)aminocarbonilo, (C₁₋₆-alquilamino)sulfonilo, di(C₁₋₆-alquil)aminosulfonilo y (C₁₋₆-alcoxi)sulfonilo, en donde las partes alifáticas y cicloalifáticas de los 15 radicales antes mencionados son no sustituidas, parcial o totalmente halogenadas, fenilo, fenil-C₁₋₆-alquilo, fenilsulfonilo, fenilaminosulfonilo, fenilcarbonilo y fenoxicarbonilo, en donde el fenilo en los últimos 6 radicales mencionados es no sustituido o sustituido con 1, 2, 3, 4 ó 5 sustituyentes idénticos o diferentes seleccionados del grupo que consiste en halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi y C₁₋₆-haloalcoxi; R² se selecciona del grupo que consiste en H, OH, S(O)₂NH₂, CN, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, (C₃₋₆-cicloalquil)-C₁₋₄-alquilo, C₁₋₆-alcoxi, (C₁₋₆-alcoxi)-C₁₋₆-alquilo, (C₁₋₆-alquil)carbonilo, (C₃₋₆-cicloalquil)carbonilo, (C₁₋₆-alcoxi)carbonilo, (C₁₋₆-alquil)sulfonilo, (C₁₋₆-alquilamino)carbonilo, di(C₁₋₆-alquil)aminocarbonilo, (C₁₋₆-alquilamino)sulfonilo, di(C₁₋₆-alquil)aminosulfonilo y (C₁₋₆-alcoxi)sulfonilo, en donde las partes alifáticas y cicloalifáticas de los 15 radicales antes mencionados son no sustituidas, parcial o totalmente halogenadas, fenilo, fenilsulfonilo, fenilaminosulfonilo, fenil-C₁₋₆-alquilo, fenoxi, fenilcarbonilo y fenoxicarbonilo, en donde el fenilo en los últimos 6 radicales mencionados es no sustituido o sustituido con 1, 2, 3, 4 ó 5 sustituyentes idénticos o diferentes seleccionados del grupo que consiste en halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi y C₁₋₆-haloalcoxi; R³ se selecciona del grupo que consiste en H, halógeno, OH, CN, C₁₋₆-alquilo, (C₁₋₆-alcoxi)-C₁₋₆-alquilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)-C₁₋₄-alquilo, C₁₋₆-alcoxi, C₂₋₆-alqueniloxi, C₂₋₆-alquiniloxi, C₃₋₆-cicloalcoxi, (C₃₋₆-cicloalquil)-C₁₋₄-alcoxi, en donde las partes alifáticas y cicloalifáticas de los 9 radicales antes mencionados son no sustituidas, parcial o totalmente halogenadas; R⁴ se selecciona del grupo que consiste en H, halógeno, CN, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₃₋₆-cicloalquilo, C₃₋₆-halocicloalquilo, C₁₋₆-alcoxi y C₁₋₆-haloalcoxi; R⁵ se selecciona del grupo que consiste en halógeno, CN, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₃₋₆-alquinilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)-C₁₋₄-alquilo, C₃₋₆-cicloalquenilo y C₁₋₆-alcoxi-C₁₋₆-alquilo, en donde las partes alifáticas y cicloalifáticas de los 7 radicales antes mencionados son no sustituidas, parcial o completamente halogenadas; o R⁴ y R⁵, junto con el átomo de carbono al que están unidos, pueden formar una porción seleccionada del grupo que consiste en carbonilo, C₃₋₆-cicloalcan-1,1-diilo, ipso-C₃₋₆-cicloalquendiilo, ipso-heterociclodiilo saturado o parcialmente insaturado de 3 a 6 miembros, en donde el carbociclo y el heterociclo son no sustituidos, parcial o totalmente halogenados, o pueden tener de 1 a 6 grupos C₁₋₆-alquilo, y la porción >C=CRˣRʸ, en donde Rˣ y Rʸ son hidrógeno, C₁₋₄-alquilo o C₁₋₄-haloalquilo; que incluye sus sales aceptables en la agricultura.
ARP150101094A 2014-04-11 2015-04-10 Compuestos de diaminotriazina AR100312A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP14164434 2014-04-11

Publications (1)

Publication Number Publication Date
AR100312A1 true AR100312A1 (es) 2016-09-28

Family

ID=50473183

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP150101094A AR100312A1 (es) 2014-04-11 2015-04-10 Compuestos de diaminotriazina

Country Status (6)

Country Link
US (1) US10941122B2 (es)
EP (1) EP3129359B1 (es)
CN (1) CN106458937A (es)
AR (1) AR100312A1 (es)
BR (1) BR112016023178B1 (es)
WO (1) WO2015155272A1 (es)

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PL3022191T3 (pl) 2013-07-16 2017-08-31 Basf Se Chwastobójcze azyny
BR112016023178B1 (pt) 2014-04-11 2021-08-24 Basf Se Composto de diaminotriazina, composição agroquímica, método para o controle de vegetação indesejada e uso de um composto
EP3129360B1 (en) 2014-04-11 2018-10-17 Basf Se Diaminotriazine derivatives as herbicides
BR112016023853A2 (pt) 2014-04-17 2017-08-15 Basf Se composto, composição, método para controlar a vegetação indesejável e uso de um composto
UA119560C2 (uk) 2014-04-23 2019-07-10 Басф Се Діамінотриазини як гербіциди
KR20160146895A (ko) 2014-04-23 2016-12-21 바스프 에스이 아진을 포함하는 제초제 조합물
US10029992B2 (en) 2014-04-23 2018-07-24 Basf Se Diaminotriazine compounds and their use as herbicides
EP3209668B1 (en) 2014-10-24 2018-07-25 Basf Se Substituted pyridine compounds having herbicidal activity
WO2016116870A1 (en) 2015-01-21 2016-07-28 Basf Se Plants having increased tolerance to herbicides
WO2017068544A1 (en) 2015-10-22 2017-04-27 Basf Se Plants having increased tolerance to herbicides
EA201990308A1 (ru) 2016-07-15 2019-07-31 Басф Се Растения с повышенной устойчивостью к гербицидам
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KR20210060514A (ko) 2018-09-18 2021-05-26 바스프 에스이 디아미노트리아진 화합물
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BR112016023178B1 (pt) 2014-04-11 2021-08-24 Basf Se Composto de diaminotriazina, composição agroquímica, método para o controle de vegetação indesejada e uso de um composto
US10029992B2 (en) 2014-04-23 2018-07-24 Basf Se Diaminotriazine compounds and their use as herbicides
KR20160146895A (ko) 2014-04-23 2016-12-21 바스프 에스이 아진을 포함하는 제초제 조합물
UA119560C2 (uk) 2014-04-23 2019-07-10 Басф Се Діамінотриазини як гербіциди

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US10941122B2 (en) 2021-03-09
CN106458937A (zh) 2017-02-22
WO2015155272A1 (en) 2015-10-15
EP3129359B1 (en) 2021-03-03
BR112016023178B1 (pt) 2021-08-24
US20170022170A1 (en) 2017-01-26
EP3129359A1 (en) 2017-02-15
BR112016023178A2 (pt) 2017-08-15

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