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AR069067A1 - AMIDA COMPOUND AND PHYTO DISEASE CONTROL USING THIS COMPOUND - Google Patents

AMIDA COMPOUND AND PHYTO DISEASE CONTROL USING THIS COMPOUND

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Publication number
AR069067A1
AR069067A1 ARP080104699A ARP080104699A AR069067A1 AR 069067 A1 AR069067 A1 AR 069067A1 AR P080104699 A ARP080104699 A AR P080104699A AR P080104699 A ARP080104699 A AR P080104699A AR 069067 A1 AR069067 A1 AR 069067A1
Authority
AR
Argentina
Prior art keywords
alkyl
group
alkoxy
alkynyl
alkenyl
Prior art date
Application number
ARP080104699A
Other languages
Spanish (es)
Inventor
Komori Takashi
Original Assignee
Sumitomo Chemical Co
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 Sumitomo Chemical Co filed Critical Sumitomo Chemical Co
Publication of AR069067A1 publication Critical patent/AR069067A1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Compuesto que posee un efecto de control sobre fitoenfermedades. Reivindicación 1: Un compuesto de amida caracterizado por la fórmula (1) en donde Q es un grupo que tiene un anillo heterocíclico fusionado y seleccionado de entre los siguientes grupos Q¹, Q² y Q³; en donde m¹ es un número entero de 0 a 6; m² es un número entero de 0 a 5; m³ es un número entero de 0 a 4; R¹ es, de modo independiente, en cada ocurrencia un átomo de halógeno, un grupo alquilo C₁₋₄, alcoxilo C₁₋₄ o ciano, que se une a un átomo de C del anillo heterocíclico fusionado; R² es, de modo independiente, en cada ocurrencia un átomo de halógeno, un grupo alquilo C₁₋₄, alcoxilo C₁₋₄ o ciano, que se une con un átomo de C del anillo heterocíclico fusionado; R³ es, de modo independiente, en cada ocurrencia un átomo de halógeno, un grupo alquilo C₁₋₄, alcoxilo C₁₋₄ o ciano, que se une con un átomo de C del anillo heterocíclico fusionado; X¹ y X³ son, de modo, independiente, un grupo metileno que puede estar sustituido con un grupo alquilo C₁₋₄ o dos grupos alquilo C₁₋₄ que pueden ser iguales o diferentes; X² es un grupo hidrocarbonado C₂₋₅ lineal divalente que tiene una valencia libre en cada átomo de carbono terminal y puede estar sustituido con uno o varios grupos seleccionados del grupo que consiste en átomos de halógeno, grupos alquilo C₁₋₄ y grupos alcoxilo C₁₋₄; Z¹ es un átomo de oxígeno o un átomo de azufre; G¹ es un enlace simple, un átomo de oxígeno, un átomo de azufre o un grupo >N-R⁴; R⁴ es un átomo de hidrógeno, un grupo alquilo C₁₋₄, alquenilo C₃₋₄, alquinilo C₃₋₄, alquil C₂₋₅-carbonilo o un grupo alcoxi C₂₋₅-carbonilo; y A¹ es un grupo alquilo C₂₋₈ que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1] descrito más abajo; un grupo alquenilo C₂₋₈ que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1]; un grupo alquinilo C₂₋₈ que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1]; un grupo cicloalquilo C₃₋₅ que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1]; o un grupo de anillo aromático de 5 a 10 miembros que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1], siempre que G¹ sea un enlace simple en el caso de que A¹ sea un grupo vinilo que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1] o un grupo etinilo que puede estar sustituido con uno o varios grupos seleccionados del grupo [a-1]; el grupo [a-1] que consiste en átomos de halógeno, grupo hidroxilo, carboxilo, amino, carbamoilo, formilo, nitro, ciano, grupos alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, alcoxilo C₁₋₆, alquenil C₃₋₆-oxi, alquinil C₃₋₆-oxi, alquil C₁₋₆-tio, alquenil C₃₋₆-tio, alquinil C₃₋₆-tio, alquil C₁₋₆-sulfinilo, alquil C₁₋₆-sulfonilo, alquil C₁₋₆-sulfoniloxi, alquil C₂₋₇-carbonilo, alcoxi C₂₋₇-carbonilo, alquil C₁₋₆aminocarbonilo, di(alquil C₁₋₆)aminocarbonilo, alquil C₂₋₇-carboniloxi, alcoxi C₂₋₇-carboniloxi, alquil C₁₋₆aminocarboniloxi, di(alquil C₁₋₆)aminocarboniloxi, alquil C₁₋₆-amino, alquenil C₃₋₆-amino, alquinil C₃₋₆-amino, alquil C₂₋₇-carbonilamino, alcoxi C₂₋₇-carbonilamino, alquil C₁₋₆-sulfonilamino, di(alquil C₁₋₆)amino, y grupos representados por la siguiente fórmula: G²-A² en donde A² es un grupo hidrocarbonado cíclico C₃₋₁₀ o un grupo heterocíclico de 5 a 10 miembros, y G² es un enlace simple, un átomo de oxígeno, un átomo de azufre o un grupo >N-R⁵, en donde R⁵ es un átomo de hidrógeno, un grupo alquilo C₁₋₄, alquenilo C₃₋₄, alquinilo C₃₋₄, alquil C₂₋₅-carbonilo o un grupo alcoxi C₂₋₅-carbonilo, en donde de los grupos que pertenecen al grupo [a-1], cada uno de los grupos alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, alcoxilo C₁₋₆, alquenil C₃₋₆-oxi, alquinil C₃₋₆-oxi, alquil C₁₋₆-tio, alquenil C₃₋₆-tio, alquinil C₃₋₆-tio, alquil C₁₋₆-sulfinilo, alquil C₁₋₆-sulfonilo, alquil C₁₋₆-sulfoniloxi, alquil C₂₋₇-carbonilo, alcoxi C₂₋₇-carbonilo, alquil C₁₋₆aminocarboniilo, di(alquil C₁₋₆)aminocarbonilo, alquil C₂₋₇-carboniloxi, alcoxi C₂₋₇-carboniloxi, alquil C₁₋₆aminocarboniloxi, di(alquil C₁₋₆)aminocarboniloxi, alquil C₁₋₆-amino, alquenil C₃₋₆-amino, alquinil C₃₋₆-amino, alquil C₂₋₇-carbonilamino, alcoxi C₂₋₇-carbonilamino, alquil C₁₋₆-sulfonilamino, di(alquil C₁₋₆)amino, y grupos representados por la fórmula G²-A² puede estar sustituido con uno o varios grupos seleccionados del siguiente grupo [a-2]; el grupo [a-2] que consiste en átomos de halógeno, grupo hidroxilo, carboxilo, amino, carbamoilo, formilo, nitro, ciano, grupos alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, alcoxilo C₁₋₆, alquenil C₃₋₆-oxi, alquinil C₃₋₆-oxi, alquil C₁₋₆-tio, alquil C₁₋₆-sulfinilo, alquil C₁₋₆-sulfonilo, alquil C₂₋₇-carbonilo, alcoxi C₂₋₇-carbonilo, alquil C₁₋₆aminocarbonilo, di(alquil C₁₋₆)aminocarbonilo, y grupos representados por la siguiente fórmula G³-A³, en donde A³ es un grupo hidrocarbonado cíclico C₃₋₁₀ o un grupo heterocíclico de 5 a 10 miembros, y G³ es un enlace simple, un átomo de oxígeno, un átomo de azufre o un grupo >N-R⁶, en donde R⁶ es un átomo de hidrógeno, un grupo alquilo C₁₋₄, alquenilo C₃₋₄, alquinilo C₃₋₄, alquil C₂₋₅-carbonilo o un grupo alcoxi C₂₋₅-carbonilo.Compound that has a phyto-disease control effect. Claim 1: An amide compound characterized by the formula (1) wherein Q is a group having a fused heterocyclic ring and selected from the following groups Q¹, Q² and Q³; where m¹ is an integer from 0 to 6; m² is an integer from 0 to 5; m³ is an integer from 0 to 4; R¹ is, independently, at each occurrence a halogen atom, a C₁₋₄ alkyl, C₁₋₄ alkoxy or cyano group, which binds to a C atom of the fused heterocyclic ring; R² is, independently, at each occurrence a halogen atom, a C₁₋₄ alkyl, C₁₋₄ alkoxy or cyano group, which binds with a C atom of the fused heterocyclic ring; R³ is, independently, at each occurrence a halogen atom, a C₁₋₄ alkyl, C₁₋₄ alkoxy or cyano group, which binds with a C atom of the fused heterocyclic ring; X¹ and X³ are, independently, a methylene group that may be substituted with a C₁₋₄ alkyl group or two C₁₋₄ alkyl groups that may be the same or different; X² is a divalent linear Crocar hydrocarbon group that has a free valence at each terminal carbon atom and may be substituted with one or more groups selected from the group consisting of halogen atoms, C₁₋₄ alkyl groups and C₁₋ alkoxy groups ₄; Z¹ is an oxygen atom or a sulfur atom; G¹ is a simple bond, an oxygen atom, a sulfur atom or a group> N-R⁴; R⁴ is a hydrogen atom, a C₁₋₄ alkyl, C₃₋₄ alkenyl, C₃₋₄ alkynyl, C₂₋₅-carbonyl alkyl or a C₂₋₅-carbonyl alkoxy group; and A¹ is a C₂₋₈ alkyl group that may be substituted with one or more groups selected from the group [a-1] described below; a C₂₋₈ alkenyl group that may be substituted with one or more groups selected from the group [a-1]; a C₂₋₈ alkynyl group which may be substituted with one or more groups selected from the group [a-1]; a C₃₋₅ cycloalkyl group that may be substituted with one or more groups selected from the group [a-1]; or a 5-10 membered aromatic ring group that may be substituted with one or more groups selected from the group [a-1], provided that G¹ is a single bond in the case that A¹ is a vinyl group that may be substituted with one or more groups selected from group [a-1] or an ethynyl group that may be substituted with one or more groups selected from group [a-1]; the group [a-1] consisting of halogen atoms, hydroxyl group, carboxyl, amino, carbamoyl, formyl, nitro, cyano, C₁₋₆ alkyl groups, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ alkoxy, C₃₋₆-oxy alkenyl, C₃₋₆-oxy alkynyl, C₁₋₆-thio alkyl, C₃₋₆-thio alkenyl, C₃₋₆-thio alkynyl, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, alkyl C₁₋₆-sulfonyloxy, C₂₋₇-carbonyl alkyl, C₂₋₇-carbonyl alkoxy, C₁₋₆aminocarbonyl alkyl, di (C₁₋₆ alkyl) aminocarbonyl, C₂₋₇-carbonyloxy alkyl, C₂₋₇-carbonyloxy alkoxy, C₁ alkyl Inoaminocarbonyloxy, di (C₁₋₆ alkyl) aminocarbonyloxy, C₁₋₆-amino alkyl, C₃₋₆-amino alkenyl, C₃₋₆-amino alkynyl, C₂₋₇-carbonylamino alkyl, C₂₋₇-carbonylamino alkoxy, C₁₋ alkyl Sulf-sulfonylamino, di (C₁₋₆ alkyl) amino, and groups represented by the following formula: G²-A² where A² is a cyclic hydrocarbon group ico C₃₋₁₀ or a 5-10 membered heterocyclic group, and G² is a single bond, an oxygen atom, a sulfur atom or a group> N-R⁵, where R⁵ is a hydrogen atom, an alkyl group C₁₋₄, C₃₋₄ alkenyl, C₃₋₄ alkynyl, C₂₋₅-carbonyl alkyl or a C₂₋₅-carbonyl alkoxy group, wherein of the groups belonging to the group [a-1], each of the groups C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ alkoxy, C₃₋₆-oxy alkenyl, C₃₋₆-oxy alkynyl, C₁₋₆-thio alkyl, C₃₋₆-thio alkenyl, C₃ alkynyl ₋₆-thio, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, C₁₋₆-sulfonyloxy alkyl, C₂₋₇-carbonyl alkyl, C₂₋₇-carbonyl alkoxy, C₁₋₆-aminocarbonyl alkyl, di (C₁₋ alkyl ₆) aminocarbonyl, C₂₋₇-carbonyloxy alkyl, C₂₋₇-carbonyloxy alkoxy, C₁₋₆-aminocarbonyloxy alkyl, di (C₁₋₆ alkyl) aminocarbonyloxy, C₁₋₆-amino alkyl, C₃₋₆-amino alkenyl, C₃₋₆-amino alkynyl, C₂₋₇-carbonylamino alkyl, C₂₋₇-carbonylamino alkoxy, C₁₋₆-sulfonylamino alkyl, di (C₁₋₆ alkyl) amino, and groups represented by the formula G²-A² may be substituted with one or more groups selected from the following group [a-2]; the group [a-2] consisting of halogen atoms, hydroxyl group, carboxyl, amino, carbamoyl, formyl, nitro, cyano, C₁₋₆ alkyl groups, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₃₋₆-oxy alkenyl, C₃₋₆-oxy alkynyl, C₁₋₆-thio alkyl, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, C₂₋₇-carbonyl alkyl, C₂₋ alkoxy Carbon-carbonyl, C₁₋₆-aminocarbonyl alkyl, di (C₁₋₆-alkyl) aminocarbonyl, and groups represented by the following formula G³-A³, wherein A³ is a C₃₋₁₀ cyclic hydrocarbon group or a 5-10 membered heterocyclic group, and G³ is a single bond, an oxygen atom, a sulfur atom or a group> N-R⁶, where R⁶ is a hydrogen atom, a C₁₋₄ alkyl group, C₃₋₄ alkenyl, C₃₋₄ alkynyl, C₂₋₅-carbonyl alkyl or a C₂₋₅-carbonyl alkoxy group.

ARP080104699A 2007-10-31 2008-10-28 AMIDA COMPOUND AND PHYTO DISEASE CONTROL USING THIS COMPOUND AR069067A1 (en)

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JP2007283068 2007-10-31

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AR069067A1 true AR069067A1 (en) 2009-12-23

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AR (1) AR069067A1 (en)
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WO (1) WO2009057668A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20140117423A (en) 2012-01-24 2014-10-07 스미또모 가가꾸 가부시끼가이샤 Plant disease control composition
CA2857464A1 (en) * 2012-01-25 2013-08-01 Sumitomo Chemical Company, Limited Plant disease control composition
SI3426032T1 (en) * 2016-03-10 2020-11-30 Syngenta Participations Ag Microbiocidal quinoline (thio)carboxamide derivatives
CN106947781B (en) * 2017-04-21 2019-08-23 云南大学 A kind of fungi intends disk stey extract and its application
BR112020004924A2 (en) * 2017-09-13 2020-09-15 Syngenta Participations Ag microbiocidal derivatives of quinoline (thio) carboxamide
JP7202366B2 (en) * 2017-09-13 2023-01-11 シンジェンタ パーティシペーションズ アーゲー Microbicidal quinoline(thio)carboxamide derivatives

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TWI314041B (en) * 2002-10-21 2009-09-01 Sankyo Agro Co Ltd Quinolyl-3-carboxamide compound

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JP2009132690A (en) 2009-06-18
CL2008003259A1 (en) 2010-02-05
WO2009057668A1 (en) 2009-05-07

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