Pesticidally active pyrrole derivatives

US11459318B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11459318-B2
Application numberUS-201816754050-A
CountryUS
Kind codeB2
Filing dateOct 4, 2018
Priority dateOct 6, 2017
Publication dateOct 4, 2022
Grant dateOct 4, 2022

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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.

Compounds of formula (I) as defined herein, to processes for preparing them, to pesticidal, in particular insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising them and to methods of using them to combat and control pests such as insect, acarine, mollusc and nematode pests.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound of formula (I), wherein R 1 is selected from H, C 1 -C 6 -alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —C 0 -C 3 -alkyl-C 3 -C 7 cycloalkyl, —C(═O)—C 1 -C 6 -alkyl, —C(═O)—O—C 1 -C 6 -alkyl, —C(═O)—N—(C 1 -C 6 -alkyl) 2 , —(C 0 -C 3 )-alkyl-aryl and —(C 0 -C 3 )-alkyl-heteroaryl, wherein each of C 1 -C 6 -alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —C 0 -C 3 -alkyl-C 3 -C 7 cycloalkyl, —C(═O)—C 1 -C 6 -alkyl, —C(═O)—O—C 1 -C 6 -alkyl, —C(═O)—N—(C 1 -C 6 -alkyl) 2 , —(C 0 -C 3 )-alkyl-aryl and —(C 0 -C 3 )-alkyl-heteroaryl is unsubstituted or substituted with 1 to 7 substituents independently selected from halogen, cyano, C 1 -C 6 -alkoxy and —C(═O)—O—C 1 -C 6 -alkyl; Q is selected from H, hydroxy, —C(═O)H, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —C 0 -C 3 -alkyl-C 3 -C 7 cycloalkyl, —C 0 -C 3 -alkyl-C 3 -C 7 heterocycloalkyl, —C 0 -C 3 -alkyl-aryl, —C 0 -C 3 -alkyl-heteroaryl, —NH—(C 1 -C 6 -alkyl), —N—(C 1 -C 6 -alkyl) 2 and —C(═O)N—(C 1 -C 6 -alkyl) 2 , wherein each of C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —C 0 -C 3 -alkyl-C 3 -C 7 cycloalkyl, —C 0 -C 3 -alkyl-C 3 -C 7 heterocycloalkyl, —C 0 -C 3 -alkyl-aryl, —C 0 -C 3 -alkyl-heteroaryl, —NH—(C 1 -C 6 -alkyl), —N—(C 1 -C 6 -alkyl) 2 and —C(═O)N—(C 1 -C 6 -alkyl) 2 is unsubstituted or substituted with 1 to 7 substituents independently selected from halogen, hydroxyl, nitro, amino, cyano, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkoxycarbonyl, —C(═O)OH, C 1 -C 6 -alkylcarbamoyl, —C(═O)NH 2 , —C(═S)NH 2 , C 3 -C 6 -cycloalkylcarbamoyl and phenyl; W is O or S; L is selected from wherein indicates the bond to the group T is selected from wherein indicates the bond to the L group; R 2 is H, Cl or Br; R 3 is selected from Cl, Br and CN; Z 1 is selected from H, C 1 -C 6 -alkyl and C 3 -C 6 -cycloalkyl wherein C 1 -C 6 -alkyl and C 3 -C 6 -cycloalkyl is unsubstituted or substituted with 1 to 9 substituents independently selected from halogen, cyano and C 1 -C 6 -alkoxy; Z 2 and Z 4 are independently selected from H, halogen, cyano, nitro, C 1 -C 6 -alkyl, —C(═S)—NH 2 , —C(═S)—NH(C 1 -C 6 -alkyl), —C(═S)—N(C 1 -C 6 -alkyl) 2 , C 3 -C 7 heterocycloalkyl, C 3 -C 6 -cycloalkyl, —S—C 1 -C 6 -alkyl, —S—C 3 -C 5 -cycloalkyl, —SO—C 1 -C 6 -alkyl, —SO—C 3 -C 5 -cycloalkyl, —SO 2 —C 1 -C 6 -alkyl, —SO 2 —C 3 -C 5 -cycloalkyl, —SO 2 —O—C 1 -C 6 -alkyl, —SO 2 —O—C 3 -C 5 -cycloalkyl, —C 0 -C 3 -alkyl-aryl, —C 0 -C 3 -alkyl-heteroaryl, wherein each of —C(═S)—NH(C 1 -C 6 -alkyl), —C(═S)—N(C 1 -C 6 -alkyl) 2 , C 1 -C 6 -alkyl, C 3 -C 7 heterocycloalkyl, C 3 -C 6 -cycloalkyl, —S—C 1 -C 6 -alkyl, —S—C 3 -C 5 -cycloalkyl, —SO—C 1 -C 6 -alkyl, —SO—C 3 -C 5 -cycloalkyl, —SO 2 —C 1 -C 6 -alkyl, —SO 2 —C 3 -C 5 -cycloalkyl, —SO 2 —O—C 1 -C 6 -alkyl, —SO 2 —O—C 3 -C 5 -cycloalkyl, —C 0 -C 3 -alkyl-aryl and —C 0 -C 3 -alkyl-heteroaryl is unsubstituted or substituted with 1 to 9 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkoxycarbonyl and hydroxycarbonyl; Z 3 is selected from H and halogen; or an agrochemically acceptable salt thereof. 2. The compound or salt according to claim 1 , wherein T is wherein indicates the bond to the L group; R 3 is selected from Cl, Br and CN. 3. The compound or salt according to claim 1 , wherein T is wherein indicates the bond to the L group; R 2 is H, Cl or Br. 4. The compound or salt according to claim 1 , wherein T is wherein indicates the bond to the L group; R 2 is H, Cl or Br. 5. The compound or salt according to claim 1 , wherein L is wherein indicates the bond to the group 6. A compound or salt according to claim 1 , wherein L is wherein indicates the bond to the group 7. The compound or salt according to claim 1 , wherein R 1 is selected from H and C 1 -C 6 -alkyl. 8. The compound or salt according to claim 1 , wherein Q is C 3 -C 6 -cycloalkyl which is unsubstituted or substituted with 1 to 3 substituents independently selected from halogen and cyano. 9. The compound or salt according to claim 1 , wherein Z 1 is C 1 -C 6 -alkyl wherein C 1 -C 6 -alkyl is unsubstituted or substituted with 1 to 7 halogen substituents; Z 2 is selected from C 1 -C 6 -alkyl which is substituted with 1 to 7 halogen substituents; Z 3 is H or bromo; Z 4 is selected from H, halogen, nitro, cyano, methyl, trifluoromethyl and —C(═S)—NH 2 . 10. The compound or salt according to claim 1 , wherein Z 1 is selected from methyl, —CH 2 CN, —CH 2 F and —CH 2 —O—CH 3 ; Z 2 is selected from —CF(CF 3 )(CF 3 ); Z 3 is H or bromo; Z 4 is selected from H, halogen, nitro, cyano, methyl, trifluoromethyl and —C(═S)—NH 2 . 11. A pesticidal composition, which comprises at least one compound according to claim 1 , or an agrochemically acceptable salt or N-oxide thereof, as active ingredient and at least one auxiliary. 12. The composition according to claim 11 , which further comprises one or more additional insecticidally, acaricidally, nematicidally and/or fungicidally active agents. 13. A method for controlling insect, acarine, mollusc, and nematode pests, which comprises applying a composition according to claim 11 to the pests or their environment with the proviso that treating human or animal bodies by surgery or therapy and/or diagnostic methods practiced on human or animal bodies are excluded. 14. A method for the protection of plant propagation material from attack by insect, acarine, mollusc, and nematode pests, which comprises treating the propaga

Assignees

Inventors

Classifications

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof · CPC title

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

  • C07D401/14Primary

    containing three or more hetero rings · CPC title

  • C07D413/04Primary

    directly linked by a ring-member-to-ring-member bond · CPC title

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What does patent US11459318B2 cover?
Compounds of formula (I) as defined herein, to processes for preparing them, to pesticidal, in particular insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising them and to methods of using them to combat and control pests such as insect, acarine, mollusc and nematode pests.
Who is the assignee on this patent?
Syngenta Participations Ag
What technology area does this patent fall under?
Primary CPC classification C07D401/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 04 2022 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).