5-halogenopyrazole indanyl carboxamides

US9375005B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9375005-B2
Application numberUS-201314399539-A
CountryUS
Kind codeB2
Filing dateMay 6, 2013
Priority dateMay 9, 2012
Publication dateJun 28, 2016
Grant dateJun 28, 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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  6. CPC / IPC classifications

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Abstract

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The present invention relates to novel 1-methyl-3-dihalogenomethyl-5-halogenopyrazole(thio)indanyl carboxamides, to processes for preparing these compounds, to compositions comprising these compounds, and to the use thereof as biologically active compounds, 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. 1-Methyl-3-dihalogenomethyl-5-halogenopyrazole(thio)indanyl carboxamide of formula (I) in which Hal 1 represents chlorine or fluorine; Hal 2 represents chlorine, bromine, or fluorine; T represents an oxygen or sulfur atom; Q represents hydrogen, C 1 -C 6 -alkylsulfonyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -haloalkylsulfonyl, halo-C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl; X 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 -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; m represents 0, 1, 2 or 3; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 independently of one another represent hydrogen, halogen; nitro; cyano; hydroxyl; amino; sulfanyl, 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; 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; 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; C 1 -C 8 -arylalkylamino 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; provided that R 1 , R 5 and R 6 do not represent methyl at the same time when R 2 , R 3 and R 4 represent hydrogen at the same time; 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 ; 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 ; R 4 and R 5 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 ; 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 ; R 1 and R 3 or R 3 and R 5 can form with the carbons 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; 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 -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; 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 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 1 -C 16 -alkyl; 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. 1-Methyl-3-dihalogenomethyl-5-halogenopyrazole(thio)indanyl carboxamide of formula (I) according to claim 1 , wherein Hal 1 represents chlorine or fluorine; Hal 2 represents chlorine, bromine, or fluorine; T represents an oxygen or sulfur 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; X represents fluorine, chlorine, iodine, methyl, cyclopropyl, or trifluoromethyl; m represents 0, 1 or 2; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 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; 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 u

Assignees

Inventors

Classifications

  • C07D231/14Primary

    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 · CPC title

  • Halogen atoms or nitro radicals · CPC title

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

  • A01N43/56Primary

    1,2-Diazoles; Hydrogenated 1,2-diazoles · CPC title

  • with condensed rings · CPC title

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What does patent US9375005B2 cover?
The present invention relates to novel 1-methyl-3-dihalogenomethyl-5-halogenopyrazole(thio)indanyl carboxamides, to processes for preparing these compounds, to compositions comprising these compounds, and to the use thereof as biologically active compounds, 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 C07D231/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 28 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).