Halogen-substituted compounds
US-10047076-B2 · Aug 14, 2018 · US
US11459318B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11459318-B2 |
| Application number | US-201816754050-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 4, 2018 |
| Priority date | Oct 6, 2017 |
| Publication date | Oct 4, 2022 |
| Grant date | Oct 4, 2022 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
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.
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
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
containing three or more hetero rings · CPC title
directly linked by a ring-member-to-ring-member bond · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.