Microbiocidal heterobicyclic derivatives

US9896454B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9896454-B2
Application numberUS-201515122740-A
CountryUS
Kind codeB2
Filing dateFeb 26, 2015
Priority dateMar 4, 2014
Publication dateFeb 20, 2018
Grant dateFeb 20, 2018

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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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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Compounds of the formula (I), wherein Y—X, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , A 1 , A 2 , A 3 , Ra and n areas defined in claim 1 . Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling infestation of plants, harvested food crops, seeds or non-living materials by phytopathogenic microorganisms, in particular fungi.

First claim

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The invention claimed is: 1. A compound of formula I: wherein each of A 1 , A 2 , and A 3 independently represents a nitrogen atom or CR 7 ; Y—X represents a radical selected from G1, G2, G3 and G4: R 1 and R 2 are each independently selected from hydrogen, halogen, cyano, C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, C 2 -C 6 alkenyl, and C 2 -C 6 alkynyl, in which the alkyl, cycloalkyl, alkenyl and alkynyl groups may be optionally substituted with 1 to 3 substituents independently selected from halogen, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio and phenoxy; or R 1 and R 2 together with the carbon atom to which they are attached represent a C 3 -C 10 cycloalkyl group (which may be optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy and phenoxy); R 3 and R 4 are each independently selected from hydrogen, halogen, hydroxyl, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 7 cycloalkyl, C 2 -C 6 alkenyl, and C 2 -C 6 alkynyl, in which the alkyl, alkoxy, cycloalkyl, alkenyl and alkynyl groups may be optionally substituted with 1 to 3 substituents independently selected from halogen, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio and phenoxy; or R 3 and R 4 together with the carbon atom to which they are attached represent C═O, C═CH 2 or C 3 -C 10 cycloalkyl (which may be optionally substituted with 1 to 3 substituents independently selected from the group consisting of a halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy and phenoxy); R 5 is hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or hydroxyl; R 6 is hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or hydroxyl; each R 7 independently represents hydrogen, cyano, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 3 -C 7 cycloalkyl, C 2 -C 6 alkynyl, or hydroxyl; each R 8 independently represents hydroxyl, halogen, cyano, amino, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 3 -C 7 cycloalkyl, C 2 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy, C 1 -C 6 alkylthio, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylcarbonyl, NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl) 2 , CO 2 H, CO 2 (C 1 -C 6 alkyl), C(O)N(C 1 -C 6 alkyl) 2 , C(O)NH(C 1 -C 6 alkyl), C(O)NH 2 , NH(C 1 -C 6 alkylcarbonyl), N(C 1 -C 6 alkylcarbonyl) 2 , aryl, heteroaryl, aryloxy or heteroaryloxy, in which the alkyl, cycloalkyl, alkenyl, alkynyl, and alkoxy groups may be optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, C 1 -C 6 alkoxy, hydroxyl, C 1 -C 6 alkylthio, C 1 -C 6 alkoxycarbonyl and phenoxy, and the aryl or heteroaryl groups may be optionally substituted with 1 to 5 substituents independently selected from the group consisting of halogen, C 1 -C 6 alkyl (which itself may be optionally substituted with 1 to 3 halogen atoms), C 1 -C 6 alkoxy, amino (which itself may be substituted with 1 or 2 groups independently selected from C 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl), nitro, cyano, hydroxyl, mercapto and C1-C 6 alkylthio; n is 0, 1, 2, 3 or 4; R a is hydrogen, C 1 -C 6 alkylcarbonyl or C 1 -C 6 alkyl, which may be optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio and phenoxy; or a salt or N-oxide thereof. 2. A compound according to claim 1 wherein one or more of A 1 , A 2 , and A 3 represents CR 7 . 3. A compound according to claim 1 wherein each R 7 independently represents hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkynyl, or hydroxyl. 4. A compound according to claim 1 wherein Y—X is G1, G2 or G4. 5. A compound according to claim 1 wherein R 1 and R 2 are each independently selected from hydrogen, cyano, C 1 -C 6 alkyl, and C 3 -C 7 cycloalkyl, in which the alkyl and cycloalkyl groups may be optionally substituted with 1 to 3 substituents independently selected from halogen, C 1 -C 6 alkoxy, and C 1 -C 6 alkylthio; or R 1 and R 2 together with the carbon atom to which they are attached represent a C 3 -C 6 cycloalkyl group. 6. A compound according to claim 1 wherein R 3 and R 4 are each independently selected from hydrogen, halogen, hydroxyl, C 1 -C 6 alkyl, and C 1 -C 6 alkoxy, in which the alkyl and alkoxy groups may be optionally substituted with 1 to 3 substituents independently selected from halogen, C 1 -C 6 alkoxy, and C 1 -C 6 alkylthio; or R 3 and R 4 together with the carbon atom to which they are attached represent C═O, or C 3 -C 7 cycloalkyl, which may be optionally substituted with 1 to 3 substituents independently selected from halogen. 7. A compound according to claim 1 wherein R 5 is hydrogen, halogen, or C 1 -C 6 alkyl. 8. A compound according to claim 1 wherein R 6 is hydrogen, halogen, or C 1 -C 6 alkyl. 9. A compound according to claim 1 wherein each R 8 independently represents hydroxyl, halogen, cyano, amino, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 3 -C 7 cycloalkyl, C 2 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy, C 1 -C 6 alkylthio, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylcarbonyl, phenyl, heteroaryl (wherein heteroaryl is pyridyl, thiophenyl, thiazolyl, imidazolyl, or oxazolyl), phenoxy or heteroaryloxy (wherein heteroaryl is pyridyl, thiophenyl, thiazolyl, imidazolyl, or oxazolyl), in which the alkyl, cycloalkyl, alkenyl, alkynyl, and alkoxy groups may be optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, C 1 -C 6 alkoxy and, hydroxyl, and the phenyl, and heteroaryl groups may be optionally substituted with 1 to 5 substituents independently selected from the group consisting of halogen, C 1 -C 6 alkyl, which itself may be optionally substituted with 1 to 3 halogen atoms, or C 1 -C 6 alkoxy; n is 0, 1, 2, or 3. 10. A compound according to claim 1 wherein R a is hydrogen or C 1 -C 6 alkyl when Y—X is G2. 11. A compound according to claim 1 wherein two or more of A 1 , A 2 , and A 3 represent CR 7 ; each R 7 independently represents hydrogen, halogen, C 1 -C 6 alkyl, or hydroxyl; Y—X is G1; R 1 and R 2 are each independently selected from C 1 -C 6 alkyl, in which the alkyl group may be optionally substituted with 1 to 3 substituents independently selected from halogen, and C 1 -C 6 alkoxy; or R 1 and R 2 together with the carbon atom to which they are attached represent a C 3 -C 6 cycloalkyl group; R 3 and R 4 are each independently selected from hydrogen, halogen, and C 1 -C 6 alkyl; or R 3 and R 4 together with the carbon atom to which they are attached represent C═O, or cyclopropyl; R 5 is hydrogen, or halogen; R 6 is hydrogen, or C 1 -C 6 alkyl; each R 8 independently represents halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, phenyl, heteroaryl (wherein heteroaryl is pyridyl, thiophenyl or thiazolyl), phenoxy or heteroaryloxy (wherein heteroaryl is pyridyl, thiophenyl or thiazolyl), in which the alkyl and alkoxy groups may be optionally substituted with 1 to 3 substituents independently selected from the group consisting of halogen, and the phenyl, and heteroaryl groups may be optionally substituted with 1 or 2 substituents independently selected from the group consisting of halogen, or C 1 -C 3 alkyl (which itself may be optionally substituted with 1 to 3 halogen atoms); and n is 0, 1, or 2; or a salt or N-oxide thereof. 12. A composition c

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Inventors

Classifications

  • C07D487/04Primary

    Ortho-condensed systems · CPC title

  • having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system · CPC title

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What does patent US9896454B2 cover?
Compounds of the formula (I), wherein Y—X, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , A 1 , A 2 , A 3 , Ra and n areas defined in claim 1 . Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preven…
Who is the assignee on this patent?
Syngenta Participations Ag
What technology area does this patent fall under?
Primary CPC classification C07D487/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 20 2018 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).