Heteroarylpiperidine and -piperazine derivatives as fungicides

US9770027B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9770027-B2
Application numberUS-201514821898-A
CountryUS
Kind codeB2
Filing dateAug 10, 2015
Priority dateAug 25, 2010
Publication dateSep 26, 2017
Grant dateSep 26, 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.

Heteroarylpiperidine and -piperazine derivatives of the formula (I) in which the symbols A, X, Y, L 1 , L 2 , G, Q, p, R 1 , R 2 and R 10 are each as defined in the description, and salts, metal complexes and N-oxides of the compounds of the formula (I), and the use thereof for controlling phytopathogenic harmful fungi and processes for preparing compounds of the formula (I).

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound of the formula (XIIIa) or a salt, metal complex, or N-oxide thereof wherein X is carbon, R 2 is hydrogen, p is 0, G is where the bond identified by “v” is bonded directly to X and where the bond identified by “w” is bonded directly to the isoxazol(in)e ring, R G1 is hydrogen, R 5 is hydrogen, L 2 is a direct bond, R 1 is phenyl which is substituted at least once by a substituent Z 4 and may otherwise be unsubstituted or substituted, where the substituents are each independently selected from Z 4 and from Z 1-2 , Z 1-2 is hydrogen, halogen, cyano, hydroxyl, —SH, nitro, —C(═O)H, —C(═O)NR 3 R 4 , —NR 3 R 4 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 3 -C 8 -cycloalkenyl, C 3 -C 8 -halocycloalkenyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 3 -C 8 -cycloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 3 -C 8 -cycloalkoxycarbonyl, C 3 -C 8 -cycloalkylaminocarbonyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 3 -C 8 -cycloalkoxy, C 3 -C 8 -halocycloalkoxy, C 2 -C 6 -alkenyloxy, C 2 -C 6 -haloalkenyloxy, C 2 -C 6 -alkynyloxy, C 2 -C 6 -haloalkynyloxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkoxy, C 1 -C 6 -alkylcarbonyloxy, C 1 -C 6 -haloalkylcarbonyloxy, C 3 -C 8 -cycloalkylcarbonyloxy, C 1 -C 6 -alkylcarbonyl-C 1 -C 4 -alkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 3 -C 6 -cycloalkylthio, C 1 -C 6 -alkylsulphonyl, C 1 -C 6 -haloalkylsulphonyl, C 3 -C 8 -cycloalkylsulphonyl, C 1 -C 6 -alkylsulphonylamino, C 1 -C 6 -haloalkylsulphonylamino, tri(C 1 -C 4 -alkyl)silyl, or -L 3 Z 3 , Z 4 is —C(═O)OH, —C(═O)NH 2 , —C(═S)NR 3 R 4 , cyano-C 1 -C 6 -alkyl, C 2 -C 6 -alkenylcarbonyloxy, C 2 -C 6 -alkynylthio, C 2 -C 6 -alkenylamino, C 2 -C 6 -alkynylamino, C 1 -C 6 -haloalkylamino, C 1 -C 6 -alkoxyamino, C 1 -C 6 -haloalkoxyamino, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -haloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonylamino, C 1 -C 6 -alkylcarbonyl(C 1 -C 6 -alkyl)amino, C 1 -C 6 -haloalkylcarbonyl(C 1 -C 6 -alkyl)amino, C 1 -C 6 -alkoxycarbonyl(C 1 -C 6 alkyl)amino, —NR 3 SO 2 Z 3 , C 2 -C 6 -alkenylthio, C 1 -C 6 -haloalkoxycarbonyl, C 1 -C 6 -alkoxy-C 1 -C 4 -alkylcarbonyl, —SF 5 , C 1 -C 6 -haloalkoxycarbonylamino, —NHC(═O)H, C 1 -C 6 -alkoxy(C 1 -C 4 -alkyl)aminocarbonyl, C 1 -C 6 -alkoxycarbonyl-C 1 -C 6 -alkoxy, —C(═NOR 7 )R 8 , —N═C(R 9 ) 2 , di(C 1 -C 6 -alkyl)aminocarbonylamino, di(C 1 -C 6 -alkyl)aminosulphonyl, di(C 1 -C 6 -haloalkyl)amino, C 1 -C 6 -alkylaminosulphonyl, C 1 -C 6 -alkylaminocarbonylamino, tri(C 1 -C 4 -alkyl)silyloxy, C 1 -C 6 -haloalkylsulphonyloxy, C 1 -C 6 -alkylsulphonyloxy, tri(C 1 -C 4 -alkyl)silyl-C 2 -C 4 -alkynyloxy, tri(C 1 -C 4 -alkyl)silyl-C 2 -C 4 -alkynyl or -L 4 Z 3 , L 3 is a direct bond, L 4 is —OCH 2 C≡C— or —C(═O)O— Z 3 is a phenyl radical, naphthalenyl or a 5- or 6-membered heteroaryl radical which may contain up to two substituents, where the substituents are each independently selected from the following list: substituents on carbon: halogen, cyano, nitro, hydroxyl, amino, —SH, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 1 -C 4 -haloalkyl, C 2 -C 4 -haloalkenyl, C 2 -C 4 -haloalkynyl, C 2 -C 4 -alkoxyalkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -haloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy, C 2 -C 6 -alkenyloxy, C 2 -C 6 -alkynyloxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkylthio, C 1 -C 4 -alkylsulphonyl, C 1 -C 4 -haloalkylsulphonyl or C 1 -C 4 -alkylamino, di(C 1 -C 4 -alkyl)amino, substituents on nitrogen: C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -haloalkenyl, C 2 -C 6 -haloalkynyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, phenyl, benzyl, C 1 -C 4 -haloalkylsulphonyl, C 1 -C 6 -alkoxycarbonyl, C 1 -C 6 -haloalkoxycarbonyl, phenylsulphonyl, C 1 -C 4 -alkylsulphonyl, —C(═O)H, or C 1 -C 3 -alkylcarbonyl, R 3 and R 4 are the same or different and are each independently hydrogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -haloalkyl, C 3 -C 8 -cycloalkyl, benzyl or phenyl, R 7 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, benzyl or Z 3 , R 8 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, C 3 -C 8 -cycloalkyl, C 1 -C 4 -alkyl-C 3 -C 8 -cycloalkyl, C 1 -C 4 -haloalkyl-C 3 -C 8 -cycloalkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -haloalkoxy-C 1 -C 4 -alkyl, benzyl or phenyl, and R 9 is the same or different and is independently C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -haloalkyl, C 3 -C 8 -cycloalkyl, benzyl or phenyl. 2. A compound according to claim 1 , wherein p is 0; X is carbon; R 2 is H; G is R G1 is H; R 5 is H; L 2 is a direct bond; and R 1 is 2-chloro-6-[(methylsulfonyl)oxy]phenyl.

Assignees

Inventors

Classifications

  • 1,3-Thiazoles; Hydrogenated 1,3-thiazoles · CPC title

  • containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof · CPC title

  • Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur (containing organo-phosphorus compounds A01N57/00) · CPC title

  • C07D417/14Primary

    containing three or more hetero rings · CPC title

  • A01N43/80Primary

    five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2 · CPC title

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What does patent US9770027B2 cover?
Heteroarylpiperidine and -piperazine derivatives of the formula (I) in which the symbols A, X, Y, L 1 , L 2 , G, Q, p, R 1 , R 2 and R 10 are each as defined in the description, and salts, metal complexes and N-oxides of the compounds of the formula (I), and the use thereof for controlling phytopathogenic harmful fungi and processes for preparing compounds of the fo…
Who is the assignee on this patent?
Bayer Cropscience Ag
What technology area does this patent fall under?
Primary CPC classification C07D417/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 26 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).