http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-045678-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_315ae544538aaeac6d1f4eed6754e4bb |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-79 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C05G3-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-79 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-04 |
| filingDate | 2004-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2005-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-045678-A1 |
| titleOfInvention | SUBSTITUTED CYCLIC DERIVATIVES |
| abstract | Compound of formula (1) and compositions comprising an insecticidally effective amount of at least a second compound, with at least one insecticidally compatible vehicle; together with the methods for controlling the insects comprising applying said compositions to a place where the insects are present or expected to be present Claim 1: A compound of formula (1), wherein -R and R4 are independently selected from hydrogen, halogen, hydroxy, C1-6 alkyl, C3-6 cycloalkyl, C2-5 alkenyl, C2-5 alkynyl, C1-3 haloalkyl, C1-3 alkoxy, C1-3 haloalkoxy, C1-3 alkylthio, C1-3 haloalkyl, alkylsulfonyl C1-3, C1-3 haloalkylsulfonyl, cyano, nitro; optionally substituted amino where the optional substituent is selected from C1-4 alkyl, C1-3 alkylcarbonyl and C1-3 alkoxycarbonyl; optionally substituted imidazolyl, optionally substituted imidazolinyl, optionally substituted oxazolinyl, optionally substituted oxazolyl, optionally substituted oxadiazolyl, optionally substituted thiazolyl, optionally substituted pyrazolyl, optionally substituted triazolyl, optionally substituted furanyl, optionally substituted diohydlanido, optionally substituted dioxolanyl, optionally substituted dioxolanyl (= E) -G, and -C (R10) -Q-R11, where E is selected from O, S, NR12, and NOR12, where R12 is hydrogen, C1-4 alkyl, C1-4 haloalkyl, aryl and arylalkyl C1-4; G is selected from hydrogen, C1-3 alkyl, C1-3 haloalkyl, C1-3 alkoxy, C1-3 alkylamino and C1-3 dialkylamino; J is selected from O, S, and NR12, where R12 is as previously described; R10 and R11 are independently selected from hydrogen, C1-4 alkyl and C1-4 haloalkyl, and R10 and R11 can be taken together with -K (CHR12) e-, where e is an integer from 2 to 4; K is selected from O, S, and NR12, where R12 is as previously described; -R1 and R3 are independently selected from hydrogen, halogen and C1-3 alkyl; -L is selected from CH2, O, S and NR16 where R16 is selected from hydrogen, C1-3 alkyl, C1-3 alkoxy C1-3 alkyl, C1-3 arylalkyl, C2-4 alkenyl C1-3 alkyl, C2 haloalkenyl 4 C1-3 alkyl, C1-3 dialkyl phosphonate, C1-3 alkylcarbonyl, halo (C1-C3) C1-3 alkylcarbonyl, C1-3 alkoxy C1-3 alkylcarbonyl, arylcarbonyl and C1-3 alkylsulfonyl; -M is selected from O, S, CH2O * and (CH2) f where the asterisk denotes attached to L, and f is an integer selected from 1, 2 and 3, provided that L and M are not simultaneously O or S; -R13 is hydrogen; -R14 and R15 are independently selected from halogen; -a is an integer selected from 0 or 1; and when a is 1, -A is O, CH2, OCH2, CH2O, OCH = CH, C (= O), S (O) g, -CH = CH-, -OC (= O) -, -OC (= O) NH-, -NHC (= O) -, -NHSO2-, and -N = CH-, NR16 or N (oxide) R16 where R16 is as described previously, and g is an integer selected from 0, 1 or 2; -b is an integer selected from 0, 1, 2, 3 or 4; -R5 and R6 are independently selected from hydrogen, halogen, C1-4 alkyl, C3-6 alkyl, C1-4 haloalkyl, or aryl; -B is a cyclic bridge group of structure (2), where Q and T are independently selected from, -CRa-, -N-, and -N (oxide) -; and U is - (CRaRb) j-, where Ra and Rb in Q, T and U are independently selected from hydrogen, hydroxy, C1-4 alkyl, C1-4 haloalkyl, C1-4 alkoxy, alkylcarbonyloxy, C1-4 alkylsulfonyl C1-4 alkyl phosphinate and C1-4 alkyl phosphonate; and j is an integer selected from 1 or 2; -c is an integer selected from 0, 1, 2, 3 or 4 and when c is 1 or more, R7 and R8 are independently selected from hydrogen, C1-4 alkyl, C1-4 haloalkyl or C1-4 alkoxy or aryl ; d is an integer selected from 0 or 1; and when d is 1, D is selected from O, CH = CH, S (O) g, HC = N, C (= O), OC (= O), C (= O) O, C (= O) NH, NR16, N (oxide) R16 and NR16C (= O), where R16 and g are as previously described; R9 is selected from C1-8 alkyl, C1-6 haloalkyl, C1-4 alkylthio, C1-4 alkoxy, C1-3 arylalkyl, C1-3 arylalkoxy, C2-6 alkenyl, C2-6 haloalkenyl, C2-6 alkynyl, cycloalkyl C3-7, C4-10 cycloalkylalkyl, C1-3 alkylamino, di (C1-3 alkyl) amino, C1-3 arylalkyl, and phenylamino, where the phenyl is optionally substituted with one or more cyano, halogen, C1-3 alkyl , C1-3 alkoxy, C1-3 haloalkyl, C1-3 haloalkoxy C1-3-S (O) g, where g is previously described, pentahalotio, trialkyl C1-3silyl, and NR16 where R16 is as previously defined; and the formula (3), where h is an integer selected from 0 or 1; A1 is selected from N, C and C =; V, W, X, Y and Z are independently selected from O, S, N, N =, C, C = or C (= O); provided that when V, W, X, Y and Z are selected from N, C or C =, then R17 to R21, inclusive, are independently selected from hydrogen, halogen, C1-6 alkyl, C2-4 alkenyl, C2 alkynyl -4, C1-6 haloalkyl, C1-6 hydroxyalkyl, C3-6 cycloalkyl, C2-4 haloalkenyl, C2-4 haloalkynyl, C1-6 alkoxy, C1-6 alkoxy C1-6 alkyl, C2-4 alkenyloxy, C2-4 alkyloxy , C1-6 haloalkoxy, C2-4 haloalkenyloxy, C2-4 haloalkyloxy, C1-6 alkylthio, pentahalotio, C1-6 alkylsulfinyl, C1-6 alkylsulfonyl, C1-6 haloalkyl, C1-6 haloalkylsulfinyl, C1-6 haloalkylsulfonyl, cyano, nitro, NRcRd, where Rc and Rd are independently selected from hydrogen, C1-6 alkyl, C1-6 haloalkyl C1-6 alkoxy, C1-6 alkylcarbonyl, C1-6 alkoxycarbonyl, and where Rc and Rd can be taken together to form a saturated or unsaturated 5 or 6-membered ring containing carbon ,, O, N or S; C1-6 alkylcarbonyl, C1-6 alkylcarbonyloxy, C1-6 alkoxycarbonyl, C1-6 alkoxycarbonyloxy, C1-6 alkoxycarbonyloxy, C1-6 alkoxycarbonyloxy, C1-6 alkylaminocarbonyl, C1-6 alkylaminocarbonyloxy, di (C1- alkyl 6) phosphinoyl, aryl, aryloxy, and arylalkoxy, when h is 1; and A1, W and Y are C = and V, X and Z are CR17 and R18 or R18 and R19 can be taken together with -CR22 = CR23CR24 = CR25-, -OCR22R23CH2-, -CH2CR22R23O-, -OCR22R23O-, -OCR22R23CR24R25O -, - OCR22R23CH = CH-, -OCR22R23CH2CH2-, -OCR22 = N-, -N = CR22O-, -ON = CR22-, -ONR22C (= O) -, -CH2-NR22C (= O) -, -C3H6 -, -C2H4 (C = O) -, -SCR22 = N-, -OCR22R23C (= O) -, -CR22 = CR23NR24-, -CR22 = NNR23u-, -N = NNR22-, and -N = CR22N = N -, to form a fused ring, where R22 to R25, inclusive, are independently selected from hydrogen, halogen, C1-3 alkyl, C1-3 haloalkyl and aryl; and the agriculturally acceptable salts thereof. |
| priorityDate | 2003-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 39.