Difluoromethyl-nicotinic- tetrahydronaphtyl carboxamides

US9428459B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9428459-B2
Application numberUS-201314652499-A
CountryUS
Kind codeB2
Filing dateDec 16, 2013
Priority dateDec 19, 2012
Publication dateAug 30, 2016
Grant dateAug 30, 2016

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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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Abstract

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The present invention relates to novel difluoromethyl-nicotinic indanyl carboxamide compounds, to processes for preparing the carboxamide compounds, to compositions comprising the carboxamide compounds, and to the use thereof as biologically actives, especially for control of harmful microorganisms in crop protection and in the protection of materials.

First claim

Opening claim text (preview).

The invention claimed is: 1. Difluoromethyl-nicotinic tetrahydronaphtyl carboxamide of formula (I) in which X 1 represents halogen; cyano; C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; C 3 -C 7 -cycloalkyl, C 3 -C 7 -halocycloalkyl having 1 to 9 identical or different halogen atoms; n represents 0, 1, 2 or 3; T represents an oxygen or sulfur atom; Q represents hydrogen, optionally substituted C 1 -C 6 -alkylsulfonyl; optionally substituted C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, optionally substituted C 1 -C 4 -haloalkylsulfonyl; R a represents hydrogen, halogen, nitro, cyano, C 1 -C 12 -alkyl; C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; C 1 -C 6 -alkoxy; C 1 -C 6 -haloalkoxy having 1 to 9 identical or different halogen atoms; C 1 -C 6 -alkylsulfanyl; C 1 -C 6 -haloalkylsulfanyl having 1 to 9 identical or different halogen atoms; C 1 -C 6 -alkylsulfonyl; C 1 -C 6 -haloalkylsulfonyl having 1 to 9 identical or different halogen atoms; C 2 -C 12 -alkenyl; C 2 -C 12 -alkynyl; C 3 -C 7 -cycloalkyl; phenyl; tri(C 1 -C 8 )alkylsilyl; tri(C 1 -C 8 )alkylsilyl-C 1 -C 8 -alkyl; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 independently of one another represent hydrogen; halogen; cyano; C 1 -C 16 -alkyl; C 1 -C 16 -haloalkyl having 1 to 9 identical or different halogen atoms; C 3 -C 8 -cycloalkyl; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkyl; (C 3 -C 8 -cycloalkyl)-C 3 -C 8 -cycloalkyl; C 2 -C 8 -alkenyl; C 2 -C 8 -alkynyl; C 2 -C 8 -alkenyl-C 1 -C 16 -alkyl; C 2 -C 8 -alkynyl-C 1 -C 16 -alkyl; C 1 -C 16 -alkoxy; C 3 -C 8 -cycloalkyloxy; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkyloxy; C 1 -C 8 -alkylsulfanyl; C 3 -C 8 -cycloalkylsulfanyl; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkylsulfanyl; C 2 -C 8 -alkenyloxy; C 3 -C 8 -alkynyloxy; aryl-C 1 -C 8 -alkyloxy which is optionally substituted by up to 6 identical or different groups R b ; aryl-C 1 -C 8 -alkylsulfanyl which is optionally substituted by up to 6 identical or different groups R b ; aryloxy which is optionally substituted by up to 6 identical or different groups R b ; arylsulfanyl which is optionally substituted by up to 6 identical or different groups R b ; (C 3 -C 8 -cycloalkyl)-C 2 -C 8 -alkenyl; (C 3 -C 8 -cycloalkyl)-C 2 -C 8 -alkynyl; optionally substituted tri(C 1 -C 8 )alkylsilyl; tri(C 1 -C 8 )alkylsilyl-C 1 -C 8 -alkyl; aryl-C 1 -C 8 -alkyl which is optionally substituted by up to 6 identical or different groups R b ; aryl-C 2 -C 8 -alkenyl which is optionally substituted by up to 6 identical or different groups R b ; aryl-C 2 -C 8 -alkynyl which is optionally substituted by up to 6 identical or different groups R b ; C 1 -C 8 -alkylamino; di-C 1 -C 8 -alkylamino; arylamino which is optionally substituted by up to 6 identical or different groups R b ; C 1 -C 8 -alkylcarbonyl C 1 -C 8 -alkylcarbonyloxy; C 1 -C 8 -alkylcarbonylamino; C 1 -C 8 -alkoxycarbonyl; C 1 -C 8 -alkyloxycarbonyloxy; C 1 -C 8 -alkylcarbamoyl; di-C 1 -C 8 -alkylcarbamoyl; C 1 -C 8 -alkylaminocarbonyloxy; di-C 1 -C 8 -alkylaminocarbonyloxy; N—(C 1 -C 8 -alkyl)hydroxycarbamoyl; C 1 -C 8 -alkoxycarbamoyl; N—(C 1 -C 8 -alkyl)-C 1 -C 8 -alkoxycarbamoyl; aryl-C 1 -C 8 -alkylamino which is optionally substituted by up to 6 identical or different groups R b ; (C 1 -C 8 -alkoxyimino)-C 1 -C 8 -alkyl; (C 2 -C 8 -cycloalkoxyimino)-C 1 -C 8 alkyl; C 1 -C 8 -alkyliminoxy; C 1 -C 8 -alkyliminoxy-C 1 -C 8 -alkyl; each of which is optionally substituted; or R 1 and R 2 can form together with the carbon to which they are attached a C 3 -C 8 -cycloalkyl; C 3 -C 8 -cycloalkenyl, or a saturated 5, 6 or 7 membered heterocycle; each of which is optionally substituted; or may represent a group ═C(Y 1 )Y 2 or a group ═N—O—R c ; or R 3 and R 4 can form together with the carbon to which they are attached a C 3 -C 8 -cycloalkyl; C 3 -C 8 -cycloalkenyl, or a saturated 5, 6 or 7 membered heterocycle; each of which is optionally substituted; or may represent a group ═C(Y 1 )Y 2 or a group ═N—O—R c ; or R 5 and R 6 can form together with the carbon to which they are attached a C 3 -C 8 -cycloalkyl; C 3 -C 8 -cycloalkenyl, or a saturated 5, 6 or 7 membered heterocycle; each of which is optionally substituted; or may represent a group ═C(Y 1 )Y 2 or a group ═N—O—R c ; or R 7 and R 8 can form together with the carbon to which they are attached a C 3 -C 8 -cycloalkyl; C 3 -C 8 -cycloalkenyl, or a saturated 5, 6 or 7 membered heterocycle; each of which is optionally substituted; or may represent a group ═C(Y 1 )Y 2 or a group ═N—O—R c or a group ═O; Y 1 and Y 2 independently of one another represent hydrogen, halogen, C 1 -C 12 -alkyl; C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; C 1 -C 8 -alkylsulfanyl; phenyl; each of which is optionally substituted; or Y 1 and Y 2 can form together with the carbon to which they are attached a C 3 -C 8 -cycloalkyl or a C 3 -C 8 -cycloalkenyl or a saturated 5, 6 or 7 membered heterocycle; each of which is optionally substituted; R b represents halogen; nitro, cyano, C 1 -C 12 -alkyl; C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; C 1 -C 6 -alkoxy; C 1 -C 6 -haloalkoxy having 1 to 9 identical or different halogen atoms; C 1 -C 6 -alkylsulfanyl; C 1 -C 6 -haloalkylsulfanyl having 1 to 9 identical or different halogen atoms; C 1 -C 6 -alkyl sulfonyl; C 1 -C 6 -haloalkylsulfonyl having 1 to 9 identical or different halogen atoms; C 2 -C 12 -alkenyl; C 2 -C 12 -alkynyl; C 3 -C 7 -cycloalkyl; tri(C 1 -C 8 )alkylsilyl; R c represents C 1 -C 16 -alkyl; C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; C 3 -C 8 -cycloalkyl; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkyl; (C 3 -C 8 -cycloalkyl)-C 3 -C 8 -cycloalkyl; C 2 -C 8 -alkenyl-C 2 -C 8 -alkynyl-C 1 -C 16 -alkyl; aryl-C 1 -C 8 -alkyl which is optionally substituted by up to 6 identical or different groups R b ; each of which is optionally substituted. 2. The difluoromethyl-nicotinic tetrahydronaphtyl carboxamide of formula (I) according to claim 1 , wherein X 1 represents halogen; C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; n represents 0, 1 or 2; T represents an oxygen atom; Q represents hydrogen, C 1 -C 4 -alkylsulfonyl, C 1 -C 3 -alkoxy-C 1 -C 3 -alkyl, C 1 -C 4 -haloalkylsulfonyl, halo-C 1 -C 3 -alkoxy-C 1 -C 3 -alkyl having in each case 1 to 9 fluorine, chlorine and/or bromine atoms; R a represents hydrogen, fluorine, chlorine, methyl or trifluoromethyl; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 independently of one another represent hydrogen, halogen; cyano; C 1 -C 16 -alkyl; C 1 -C 6 -haloalkyl having 1 to 9 identical or different halogen atoms; C 3 -C 8 -cycloalkyl; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkyl; (C 3 -C 8 -cycloalkyl)-C 3 -C 8 -cycloalkyl; C 2 -C 8 -alkenyl; C 2 -C 8 -alkynyl; C 2 -C 8 -alkenyl-C 1 -C 16 -alkyl; C 2 -C 8 -alkynyl-C 1 -C 16 -alkyl; C 1 -C 16 -alkoxy; C 3 -C 8 -cycloalkyloxy; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkyloxy; C 1 -C 8 -alkylsulfanyl; C 3 -C 8 -cycloalkylsulfanyl; (C 3 -C 8 -cycloalkyl)-C 1 -C 8 -alkylsulfanyl; C 2 -C 8 -alkenyloxy; C 3 -C 8 -alkynyloxy; C 1 -C 8 -arylalkyloxy which is optionally substituted by up to 6 identical or different groups R b ; C 1 -C 8 -arylalkylsulfanyl which is optionally substituted by up to 6 identical or different groups R b ; aryloxy which is optionally substituted by up to 6 identical or different groups R b ; arylsulfanyl which is optionally substituted by up to 6 identical or different groups R b ; (C 3 -C 8 -cycloalkyl)-C 2 -C 8 -alkenyl; (C 3 -C 8 -cycloalkyl)-C 2 -C 8 -alkynyl; tri(C 1 -C 8 )alkylsilyl; tri(C 1 -C 8 )al

Assignees

Inventors

Classifications

  • six-membered rings · CPC title

  • Thioacids; Thioesters; Thioamides; Thioimides · CPC title

  • C07D213/82Primary

    in position 3 · CPC title

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What does patent US9428459B2 cover?
The present invention relates to novel difluoromethyl-nicotinic indanyl carboxamide compounds, to processes for preparing the carboxamide compounds, to compositions comprising the carboxamide compounds, and to the use thereof as biologically actives, especially for control of harmful microorganisms in crop protection and in the protection of materials.
Who is the assignee on this patent?
Bayer Cropscience Ag
What technology area does this patent fall under?
Primary CPC classification C07D213/82. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 30 2016 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).