http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2371356-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0bf0928b608797b70bbc2b91c7e52e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 |
| filingDate | 2006-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2011-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_649291624c1e72f213cb72c41d93b57f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3be12cfa40b9da46f0fa3dee4efd4ed http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e225ad158b4122d2ceda16687a2ec5ce http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c397cdf66877f3c3eaaa3b1b3c48745c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c50bc9d70ef8e2f49882e01a88e07f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e19d1ef58f6990f08f11054f1a5a978 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b886855c041ea8b5396705b45aef54a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_796bbef6f2281c9736161e18cd83b8b6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa8ea2282a3156d7c24799b50e7476f5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_460d16680d0bc385ede1de3bf33fc69e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e565ca17b6c4ed9c4ebf16b406433a6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec153ce9cd41c27c66d3fd4250b8b2b5 |
| publicationDate | 2011-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2371356-T3 |
| titleOfInvention | N-TIO-ANTRANILAMIDE COMPOUNDS AND ITS USE AS PESTICIDES. |
| abstract | N-Thio-anthranilamide compounds of formula I wherein R 1 is hydrogen; or C1-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, or C3-C8 cycloalkyl, each of which is substituted or unsubstituted with 1 to 5 independent groups selected from halogen, cyano, nitro, hydroxy, alkoxy C1-C10, C1-C10 alkylthio, C1-C10 alkylsulfinyl, C1-C10 alkylsulfonyl, C2-C10 alkoxycarbonyl, C1-C10 alkylamino, di (C1-C10 alkyl) amino and C3-C8 cycloalkylamino; or C1-C10 alkylcarbonyl, C1-C10 alkoxycarbonyl C1-C10 alkylaminocarbonyl, di (C1-C10 alkyl) aminocarbonyl; A is A1 where it indicates the binding site; R2 and R3 each independently are R6, or R2 and R3 together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3 to 8-membered ring containing 1 to 4 heteroatoms selected from oxygen, nitrogen , sulfur, whose ring may be fused with one or two rings of 5 to 6 saturated, partially unsaturated or unsaturated members that may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, where all the previous rings are substituted or not substituted by any combination of 1 to 6 R8 groups; G is oxygen or sulfur; R6 is C1-C20 alkyl, C2-C20 alkenyl, C2-C20 alkynyl, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, C3-C8 cycloalkynyl, phenyl, naphthyl, biphenyl, or a 3- to 8-membered saturated ring system, partially unsaturated or unsaturated containing 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, where all these groups are substituted or unsubstituted by a combination of 1 to 6 R8 groups; R8 is R9; or two R8 groups together with the atoms to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system that may contain from 1 to 4 heteroatoms / heterogroups selected from oxygen, nitrogen, sulfur, SO and SO2, and whose ring system is substituted or unsubstituted with any combination of 1 to 6 R9 groups. R9 is R10, R11, -C (= G) R10, -C (= NOR10) R10, -C (= NNR10 2) R10, -C (= G) OR10, - C (= G) NR10 2, -OC (= G) R10, -OC (= G) OR10, -NR10C (= G) R10, -N [C (= G) R10] 2, -NR10C (= G) OR10, -C (= G) NR10- NR10 2, -C (= G) NR10-NR10 [C (= G) R10], -NR10- C (= G) NR10 2, -NR10-NR10C (= G) R10, -NR10-N [C (= G) R10] 2, -N [(C = G) R10] -NR10 2, - NR10-NR10 [(C = G) GR10], - NR10 [(C = G) NR10 2, -NR10 [C = NR10 ] R10, - NR10 (C = NR10) NR10 2, -O-NR10 2, -O-NR10 (C = G) R10, -SO2NR10 2, -NR10SO2R10, -SO2OR10, -OSO2R10, -OR10, -NR10 2, -SR10, -SiR10 3, -PR10 2, -P (= G) R10, -SOR10, - SO2R10, -PG2R10 2, -PG3R10 2, or two R9 groups together are (= G), (= N-R10) , (= CR10 2), (= CHR10), or (= CH2); E06764009 R10 is C1-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, C3-C8 cycloalkyl, C4-C8 cycloalkenyl, C3-C8 cycloalkyl-C1-C4 alkyl, C4-C8 cycloalkenyl-C1-C4 alkyl, C3 cycloalkyl - C8 - C2 - C4 alkenyl, C4 - C8 cycloalkenyl C2 - C4 alkenyl, C1 - C10 alkyl - C3 - C8 cycloalkyl, C2 - C10 alkenyl - C3 - C8 alkynyl, C2 - C10 alkynyl - C3 - C8 alkyl - C10 - C4 - C8 cycloalkenyl, C2 - C10 alkenyl C4 - C8 cycloalkenyl, C2 - C10 alkynyl C4 - C8 cycloalkenyl, a 3 to 8 membered saturated, partially unsaturated or unsaturated ring system containing 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein the above groups are substituted or unsubstituted with any combination of 1 to 6 R11 groups; R11 is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl, C1-C10 alkylcarbonyl, C1-C10 alkoxy, C2-C10 alkenyloxy, C2-C10 alkynyloxy, C1-C10 haloalkoxy, C3-C10 haloalkyloxy , C3-C8 cycloalkoxy, C4-C8 cycloalkenyloxy, C3-C8 halocycloalkoxy, C4-C8 halocycloalkoxy, C3-C8-C1-C4 alkoxy, C4-C8-C1-C4 alkoxy, C3-C2-C4-alkenyl cycloalkyl , C4-C8 cycloalkenyl C2-C4 alkenyloxy, C1-C10 alkyl-C3-C8 cycloalkoxy, C1-C10 alkenyl, C3-C8 alkynyl, C1-C10 alkynyl C3-C8 alkyl, C1-C10 alkyl-C3-C8 alkyl , C1-C10 alkenyl-C3-C8 cycloalkenyloxy, C1-C4 alkoxy-C1-C10 alkoxy, C1-C4 alkoxy-C2-C10 alkoxy, mono or di (C1-C10 alkyl) carbamoyl, mono or di (C1-C10 haloalkyl) ) carbamoyl, mono or di (C3-C8 cycloalkyl) carbamoyl, C1-C10 alkoxycarbonyl, C3-C8 cycloalkoxycarbonyl, C1-C10 alkylcarbonyloxy, cycloalkylcarb C3-C8 onyloxy, C1-C10 haloalkoxycarbonyl, C1-C10 haloalkylcarbonyloxy, C1-C10 alkanoid, C1-C10 haloalkamido, C2-C10 alkenamide, C3-C8 cycloalkylidene, C3-C8 cycloalkyl-C1-C4 alkyl-C1-C10 alkylthio, C2-C10 alkenylthio, C2-C10 alkynylthio, C1-C10 haloalkylthio, C2-C10 haloalkylthio, C2-C10 haloalkylthio, C3-C8 cycloalkylthio, C3-C8 cycloalkylthio, C8-C8-C8-cycloalkyl-cycloalkyl C1-C4 alkylthio, C4-C8 cycloalkenyl C1-C4 alkylthio, C3-C8 cycloalkyl C2-C4 alkenylthio, C4-C8 cycloalkenyl C2-C4 alkynyl, C1-C10 alkyl-C3-C8 alkenylthio, C1-C10 alkenyl C3-C8 cycloalkylthio, C1-C10 alkynyl-C3-C8-cycloalkylthio, C1-C10-alkyl-C3-C8-cycloalkenylthio, C3-C8-alkenyl, C1-C10-cycloalkenylthio, C2-C10-alkylsulfinyl, C2-C10 alkylsulfin C1-C10 haloalkylsulfinyl, C2-C10 haloalkenylsulfinyl, haloa C2-C10 alkylsulfinyl, C3-C8 cycloalkylsulfinyl C3-C8 cycloalkenylsulfinyl C3-C8, halocycloalkylsulfinyl C3-C8, C3-C8-cycloalkyl-C1-C4-alkylsulfinyl C-C4-C4-cycloalkenyl-C4-C4-C3-C4-cycloalkenyl groups - C2-C4 alkenylsulfinyl, C4-C8 cycloalkenyl C2-C4 alkylsulfinyl C1-C10 alkyl-C3-C8 cycloalkylsulfinyl, C3-C8 alkenyl, C1-C10-cycloalkylsulfinyl C3-C10-cycloalkylsulfinyl, C3-C8-alkyl-C3-C10 alkyls - C3-C8 cycloalkenylsulfinyl, C1-C10 alkenyl-C3-C8 cycloalkenylsulfinyl, C1-C10 alkylsulfonyl, C2-C10 alkylsulfonyl, C2-C10 alkylsulfonyl, C2-C10-C10-C-alkylsulfonyl, C2-cyclo-C-C-alkylsulfonyl , C3-C8 cycloalkenylsulfonyl, C3-C8 halocycloalkylsulfonyl, C3-C8 halocycloalkenyl sulfonyl, C3-C8 cycloalkyl-C1-C4 alkylsulfonyl, C4-C8 alkylsulfonyl C1-C4, C3-C8 cycloalkyl C2-C4 alkenylsulfonyl C4-C8 cycloalkenyl C2-C4 alkylsulfonyl C3-C8 alkyl, C1-C10-cycloalkylsulfonyl C3-C8-alkynyl-C8-alkynyl C3-C8, C1-C10 alkyl-C3-C8 cycloalkenylsulfonyl, C1-C10 alkenyl C3-C8 cycloalkenylsulfonyl, amino (C1-C10) amino, C1-C10 alkylamino, C2-C10 alkylamino, C2-C10 alkylamino - C10 - C2-C10 alkenylamino, C1-C10 alkyl-C2-C10 alkylamino, C1-C10 haloalkylamino, C2-C10 haloalkylamino, C2-C10 haloalkylamino, C3-C8 cycloalkylamino, C3-C8 alkenyl halocycloalkylamino - C8, C3-C8 cycloalkyl-C1-C4 alkylamino, C4-C8 cycloalkenyl-C1-C4 alkylamino, C3-C8 cycloalkyl C2-C4 alkylamino, C2-C4 cycloalkenyl, C1-C10-alkylamino amino - C8, C1-C10 alkenyl - C3 cycloalkylamino - C8, C1-C10 alkynyl-C3-C8 cycloalkylamino, C1-C10 alkyl-C3-C8 cycloalkenylamino, C1-C10 alkenyl C3-C8 cycloalkenylamino, tri (C1-C10 alkyl) silyl, aryl, aryloxy, arylthio, arylamino, C1-C4 arylalkoxy, C3-C4 arylalkenyloxy, C1-C4 arylalkylthio, C2-C4 arylalkylthio, C1-C4 arylamino alkylamino, C3-C4 arylalkenylamino, trilylsilyl, where aryl is phenyl or biphenyl , or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system containing from 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein these aryl and these heterocyclic ring systems are substituted or unsubstituted with any combination of 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C1-C4 alkyl, C1-C4 holoalkyl, C3-C8 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio , C1-C4 haloalkylthio, di (C1-C4 alkyl) amino, C1-C4 alkylamino, C1-C4 haloalkylamino, formyl and C1-C4 alkylcarbonyl; Q1 and Q2 are each independently hydrogen, halogen, cyano, SCN, nitro, hydroxy, C1-C10 alkyl, C1-C10 haloalkyl, C2-C10 alkenyl, C2-C10 haloalkenyl, C2-C10 alkynyl, C3-C10 haloalkynyl, cycloalkyl C3-C8, C3-C8 halocycloalkyl, C1-C10 alkoxy, C1-C10 haloalkoxy, C1-C10 alkylthio, C1-C10 haloalkylthio C1-C10 alkylsulfinyl, C1-C10 haloalkylsulfinyl, C1-C10 alkylsulfonyl, C1-C10 haloalkylsulfonyl C1-C10, C1-C10 haloalkylsulfonyloxy, C1-C10 alkylamino, di (C1-C10 alkyl) amino, C3-C8 cycloalkylamino, C1-C10 alkoxycarbonyl, C1-C10 alkylaminocarbonyl, di (C1-C10 alkyl) aminocarbonyl, or trialkylsilyl (C1-C10, or Q1 and Q2 are each independently phenyl, benzyl or phenoxy, wherein each ring is substituted or unsubstituted with any combination of 1 to 3 independent substituents selected from the group of halogen, cyano, nitro, C1-C10 alkyl, haloa C1-C10 alkyl, C2-C10 alkenyl, C2-C10 haloalkenyl, C2-C10 alkynyl, C3-C10 haloalkynyl, C3-C8 cycloalkyl, C3-C8 halocycloalkyl, C1-C10 alkoxy, C1-C10 haloalkoxy, C1-C10 alkylthio alkyl, C1-C10 alkylsulfinyl, C1-C10 alkylsulfonyl, C1-C10 alkylamino, di (C1-C10 alkyl) amino, C3-C8 cycloalkylamino, C1-C10 alkyl-C3-C8 cycloalkylamino, alkylcarb |
| priorityDate | 2005-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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