Fungicide N-cycloalkyl-N-bicyclicmethylene-carboxamide derivatives

US9686985B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9686985-B2
Application numberUS-201615257734-A
CountryUS
Kind codeB2
Filing dateSep 6, 2016
Priority dateMar 26, 2012
Publication dateJun 27, 2017
Grant dateJun 27, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to N-cycloalkyl-N-bicyclicmethylene-carboxamide or thiocarboxamide derivatives, their process of preparation, preparation of intermediate compounds, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of formula (IIf) wherein W represents CZ 7 ; Y 1 and Y 2 independently represents a hydrogen atom, a halogen atom, cyano, substituted or non-substituted C 1 -C 8 -alkyl, C 1 -C 8 -halogenoalkyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkoxy, C 1 -C 8 -halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkoxycarbonyl, C 1 -C 8 -halogenoalkoxycarbonyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkylaminocarbonyl, substituted or non-substituted di-C 1 -C 8 -alkylaminocarbonyl or carbamoyl; L 1 and L 2 independently represent CZ 4 Z 5 , NZ 6 , O, S, S(O) or S(O) 2 ; m represents 1, 2 or 3; p represents 1, 2 or 3, Z 3 and Z 7 independently represents a hydrogen atom, a halogen atom; nitro; cyano; isonitrile; hydroxy; amino; sulfanyl; pentafluoro-λ 6 -sulfanyl; formyl; formyloxy; formylamino; substituted or non-substituted (hydroxyimino)-C 1 -C 8 -alkyl; substituted or non-substituted (C 1 -C 8 -alkoxyimino)-C 1 -C 8 -alkyl; substituted or non-substituted (C 2 -C 8 -alkenyloxyimino)-C 1 -C 8 -alkyl; substituted or non-substituted (C 2 -C 8 -alkynyloxyimino)-C 1 -C 8 -alkyl; substituted or non-substituted (benzyloxyimino)-C 1 -C 8 -alkyl; carboxy; carbamoyl; N-hydroxycarbamoyl; carbamate; substituted or non-substituted C 1 -C 8 -alkyl; C 1 -C 8 -halogenoalkyl having 1 to 9 halogen atoms; substituted or non-substituted C 2 -C 8 -alkenyl; C 2 -C 8 -halogenoalkenyl having 1 to 9 halogen atoms; substituted or non-substituted C 2 -C 8 -alkynyl; C 2 -C 8 -halogenoalkynyl having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkoxy; C 1 -C 8 -halogenoalkoxy having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylsulfanyl; C 1 -C 8 -halogenoalkylsulfanyl having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylsulfinyl; C 1 -C 8 -halogenoalkylsulfinyl having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylsulfonyl; C 1 -C 8 -halogenoalkylsulfonyl having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylamino; substituted or non-substituted di-C 1 -C 8 -alkylamino; substituted or non-substituted C 2 -C 8 -alkenyloxy; C 2 -C 8 -halogenoalkenyloxy having 1 to 9 halogen atoms; substituted or non-substituted C 3 -C 8 -alkynyloxy; C 2 -C 8 -halogenoalkynyloxy having 1 to 9 halogen atoms; substituted or non-substituted C 3 -C 7 -cycloalkyl; C 3 -C 7 -halogenocycloalkyl having 1 to 9 halogen atoms; substituted or non-substituted C 4 -C 7 -cycloalkenyl; C 4 -C 7 -halogenocycloalkenyl having 1 to 9 halogen atoms; substituted or non-substituted (C 3 -C 7 -cycloalkyl)-C 1 -C 8 -alkyl; substituted or non-substituted (C 3 -C 7 -cycloalkyl)-C 2 -C 8 -alkenyl; substituted or non-substituted (C 3 -C 7 -cycloalkyl)-C 2 -C 8 -alkynyl; substituted or non-substituted tri(C 1 -C 8 )alkylsilyl; substituted or non-substituted tri(C 1 -C 8 )alkylsilyl-C 1 -C 8 -alkyl; substituted or non-substituted C 1 -C 8 -alkylcarbonyl; C 1 -C 8 -halogenoalkylcarbonyl having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylcarbonyloxy; C 1 -C 8 -halogenoalkylcarbonyloxy having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylcarbonylamino; C 1 -C 8 -halogenoalkylcarbonylamino having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkoxycarbonyl; C 1 -C 8 -halogenoalkoxycarbonyl having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkyloxycarbonyloxy; C 1 -C 8 -halogenoalkoxycarbonyloxy having 1 to 9 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylcarbamoyl; substituted or non-substituted di-C 1 -C 8 -alkylcarbamoyl; substituted or non-substituted C 1 -C 8 -alkylaminocarbonyloxy; substituted or non-substituted di-C 1 -C 8 -alkylaminocarbonyloxy; substituted or non-substituted N—(C 1 -C 8 -alkyl)hydroxy carbamoyl; substituted or non-substituted C 1 -C 8 -alkoxycarbamoyl; substituted or non-substituted N—(C 1 -C 8 -alkyl)-C 1 -C 8 -alkoxycarbamoyl; aryl that can be substituted by up to 6 groups Q which can be the same or different; aryl-C 1 -C 8 -alkyl that can be substituted by up to 6 groups Q which can be the same or different; aryl-C 2 -C 8 -alkenyl that can be substituted by up to 6 groups Q which can be the same or different; aryl-C 2 -C 8 -alkynyl that can be substituted by up to 6 groups Q which can be the same or different; aryloxy that can be substituted by up to 6 groups Q which can be the same or different; arylsulfanyl that can be substituted by up to 6 groups Q which can be the same or different; arylamino that can be substituted by up to 6 groups Q which can be the same or different; aryl-C 1 -C 8 -alkyloxy that can be substituted by up to 6 groups Q which can be the same or different; aryl-C 1 -C 8 -alkylsulfanyl that can be substituted by up to 6 groups Q which can be the same or different; aryl-C 1 -C 8 -alkylamino that can be substituted by up to 6 groups Q which can be the same or different; pyridinyl which can be substituted by up to 4 groups Q; or pyridinyloxy which can be substituted by up to 4 groups Q; Z 4 and Z 5 independently represents a hydrogen atom, a halogen atom, cyano, nitro, substituted or non-substituted C 1 -C 8 -alkyl, C 1 -C 8 -halogenoalkyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkoxy, C 1 -C 8 -halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkoxy-C 1 -C 8 -alkyl, substituted or non-substituted C 2 -C 8 -alkenyl, C 2 -C 8 -halogenoalkenyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 2 -C 8 -alkynyl, C 2 -C 8 -halogenoalkynyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 3 -C 7 -cycloalkyl, substituted or non-substituted C 3 -C 7 -cycloalkyl-C 1 -C 8 -alkyl, C 3 -C 7 -halogenocycloalkyl comprising up to 9 halogen atoms that can be the same or different, formyl, substituted or non-substituted C 1 -C 8 -alkylcarbonyl, C 1 -C 8 -halogenoalkylcarbonyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkylsulfanyl, C 1 -C 8 -halogenoalkylsulfanyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkylsulfinyl, C 1 -C 8 -halogenoalkylsulfinyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkylsulfonyl, or C 1 -C 8 -halogenoalkylsulfonyl comprising up to 9 halogen atoms that can be the same or different, Z 6 represents a hydrogen atom, substituted or non-substituted C 1 -C 8 -alkyl, C 1 -C 8 -halogenoalkyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkoxy-C 1 -C 8 -alkyl, substituted or non-substituted C 2 -C 8 -alkenyl, C 2 -C 8 -halogenoalkenyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 2 -C 8 -alkynyl, C 3 -C 8 -halogenoalkynyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 3 -C 7 -cycloalkyl, substituted or non-substituted C 3 -C 7 -cycloalkyl-C 1 -C 8 -alkyl, C 3 -C 7 -halogenocycloalkyl comprising up to 9 halogen atoms that can be the same or different, formyl, substituted or non-substituted C 1 -C 8 -alkylcarbonyl, C 1 -C 8 -halogenoalkylcarbonyl comprising up to 9 halogen atoms that can be the same or different, substituted or non-substituted C 1 -C 8 -alkylsulfonyl, C 1 -C 8 -halogenoalkylsulfon

Assignees

Inventors

Classifications

  • Antimycotics · CPC title

  • the other ring being five-membered, e.g. indane · CPC title

  • Benzothiopyrans; Hydrogenated benzothiopyrans · CPC title

  • linked by a chain containing hetero atoms as chain links · CPC title

  • C07D231/16Primary

    Halogen atoms or nitro radicals · CPC title

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What does patent US9686985B2 cover?
The present invention relates to N-cycloalkyl-N-bicyclicmethylene-carboxamide or thiocarboxamide derivatives, their process of preparation, preparation of intermediate compounds, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.
Who is the assignee on this patent?
Bayer Ip Gmbh
What technology area does this patent fall under?
Primary CPC classification C07D231/16. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).