N-hetarylmethyl pyrazolylcarboxamides

US9320276B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9320276-B2
Application numberUS-201113882718-A
CountryUS
Kind codeB2
Filing dateNov 2, 2011
Priority dateNov 2, 2010
Publication dateApr 26, 2016
Grant dateApr 26, 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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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to N-Hetarylmethyl pyrazolylcarboxamides derivatives or their thiocarboxamides derivatives, their process of preparation, their use as fungicide, particularly in the form of compositions. Formula (I), 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 (I) wherein T represents O or S; X 1 and X 2 which can be the same or different, represent a chlorine or a fluorine atom; Z 1 represents a hydrogen atom, substituted or non substituted C 1 -C 8 -alkyl; substituted or non substituted C 1 -C 8 -alkoxy; substituted or non substituted C 2 -C 8 -alkenyl; substituted or non substituted C 2 -C 8 -alkynyl; substituted or non substituted C 3 -C 7 -cycloalkyl; substituted or non substituted C 3 -C 7 -cycloalkyl-C 1 -C 8 -alkyl; substituted or non substituted 3-oxetanyl; or substituted or non substituted 3-thietanyl; Z 2 and Z 3 , which can be the same or different, represent a hydrogen atom; substituted or non substituted C 1 -C 8 -alkyl; substituted or non substituted C 2 -C 8 -alkenyl; substituted or non substituted C 2 -C 8 -alkynyl; cyano; isonitrile; nitro; a halogen atom; substituted or non substituted C 1 -C 8 -alkoxy; substituted or non substituted C 2 -C 8 -alkenyloxy; substituted or non substituted C 2 -C 8 -alkynyloxy; substituted or non substituted C 3 -C 7 -cycloalkyl; substituted or non substituted C 1 -C 8 -alkylsulfanyl; substituted or non substituted C 1 -C 8 -alkylsulfony; substituted or non substituted C 1 -C 8 -alkylsulfinyl; amino; substituted or non substituted C 1 -C 8 -alkylamino; substituted or non substituted di-C 1 -C 8 -alkylamino; substituted or non substituted C 1 -C 8 -alkoxycarbonyl; substituted or non substituted C 1 -C 8 -alkylcarbamoyl; substituted or non substituted di-C 1 -C 8 -alkylcarbamoyl; or substituted or non substituted N—C 1 -C 8 -alkyl-C-C 8 -alkoxy-carbamoyl; or Z 2 and Z 3 together with the carbon atom to which they are linked form a substituted or non substituted C 3 -C 7 cycloalkyl; or Z 3 and the substituent X vicinal to the point of attachment of the B group, together with the consecutive carbon atoms to which they are linked can form a substituted or non substituted 5-, 6- or 7-membered, partly saturated, carbo- or hetero-cycle comprising up to 3 heteroatoms and Z 2 is as herein described; B represents a saturated, partially saturated or unsaturated, monocyclic or fused bicyclic 4-, 5-, 6-, 7-, 8-, 9-, 10-membered ring comprising from 1 up to 4 heteroaroms selected in the list consisting of N, O, S, that can be substituted by up to 6 groups X which can be the same or different; with the provisio that B is not a 2-pyridyl ring , and that B is not a 1,3-benzodioxolyl ring when Z 1 represents a substituted or non substituted cyclopropyl group ;X represents a halogen atom; nitro; cyano; isonitricle; 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 5 halogen atoms; substituted or non-substituted C 2 -C 8 -alkenyl; C 2 -C 8 -halogenoalkenyl having 1 to 5 halogen atoms; substituted or non-substituted C 2 -C 8 -alkynyl; C 2 -C 8 -halogenoalkynyl having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkoxy; C 1 -C 8 -halogenoalkoxy having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylsulfanyl; C 1 -C 8 -halogenoalkylsulfanyl having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylsulfinyl; C 1 -C 8 -halogenoalkylsulfinyl having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylsulfonyl; C 1 -C 8 -halogenoalkylsulfonyl having 1 to 5 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 5 halogen atoms; substituted or non-substituted C 3 -C 8 -alkynyloxy; C 2 -C 8 -halogenoalkynyloxy having 1 to 5 halogen atoms; substituted or non-substituted C 3 -C 7 -cycloalkyl; C 3 -C 7 -halogenocycloalkyl having 1 to 5 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 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylcarbonyloxy; C 1 -C 8 -halogenoalkylcarbonyloxy having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkylcarbonylamino; C 1 -C 8 -halogenoalkyl-carbonylamino having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkoxycarbonyl; C 1 -C 8 -halogenoalkoxycarbonyl having 1 to 5 halogen atoms; substituted or non-substituted C 1 -C 8 -alkyloxycarbonyloxy; C 1 -C 8 -halogenoalkoxycarbonyloxy having 1 to 5 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; C 1 -C 8 -arylalkyl that can be substituted by up to 6 groups Q which can be the same or different; C 2 -C 8 -arylalkenyl that can be substituted by up to 6 groups Q which can be the same or different; C 2 -C 8 -arylalkynyl 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; C 1 -C 8 -arylalkyloxy that can be substituted by up to 6 groups Q which can be the same or different; C 1 -C 8 -arylalkylsulfanyl that can be substituted by up to 6 groups Q which can be the same or different; or C 1 -C 8 -arylalkylamino that can be substituted by up to 6 groups Q which can be the same or different; or two substituents X together with the consecutive carbon atoms to which they are linked can form a 5- or 6-membered saturated carbocycle which can be substituted by up to four groups Q which can be the same or different; or Z 3 and the substituent X vicinal to the point of attachment of the B group, together with the consecutive carbon atoms to which they are linked can form a substituted or non substituted 5-, 6- or 7-membered, partly saturated, carbo- or hetero-cycle comprising up to 3 heteroatoms and Z 2 is as herein described; Q independently represents a halogen atom; cyano; nitro; substituted or non-substituted C 1 -C 8 -alkyl; C 1 -C 8 -halogenoalkyl having 1 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 having 1 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 having 1 to 9 halogen atoms that can be the same or different; 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-s

Assignees

Inventors

Classifications

  • 1,2-Diazines; Hydrogenated 1,2-diazines · CPC title

  • five-membered rings with three ring hetero atoms · CPC title

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

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

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

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What does patent US9320276B2 cover?
The present invention relates to N-Hetarylmethyl pyrazolylcarboxamides derivatives or their thiocarboxamides derivatives, their process of preparation, their use as fungicide, particularly in the form of compositions. Formula (I), and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.
Who is the assignee on this patent?
Benting Jurgen, Cristau Pierre, Dahmen Peter, and 5 more
What technology area does this patent fall under?
Primary CPC classification C07D401/12. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 26 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).