http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2022322-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bfacf7468cc8f61c5c219de3b28a5130 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97b5e5614b24fc989fbe6766987baa88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4c0a8c5984fd72dca38eac243e2de068 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f999d69c3e82dd22b7b8e93f1e0818d7 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N55-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-10 |
| filingDate | 1990-07-25^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c7f1c8d802e333d8b2f98431ccc8413 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_195078757c94bfcbef68bc941bc89105 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e43edcb790a77eea0434dbd12c4e7aa4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f11d6ac4c9f05a2896a31404e4f3f22 |
| publicationDate | 1991-01-28^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-2022322-A1 |
| titleOfInvention | Naphthyridine derivatives |
| abstract | Abstract Substituted naphthyridines of the formula (1): (1) wherein one of A, B, E, or D is N, and the others are CRl; R1 and R2 are independently H or halo. X is O, S, SO, SO2, NR3, or CR4R5, where R3 is H, (C1-C4) alkyl, or (C1-C4) acyl, and R4 and R5 are in-dependently H, (C1-C4) acyl, (C1-C4) alkyl, (C2-C4) alk-enyl or -alkynyl, CN, or OH, or R4 and R5 combine to form a carbocyclic ring containing four to six carbon atoms; Y is nil, Z being bonded directly to X, or Y is an alkyl chain one to six carbon atoms long, option-ally including a carbocyclic ring, and optionally includ-ing a hetero atom selected from O, S, SO, SO2, NR3, or SiR19R20, where R19 and R20 are independently H, (C1-C4) alkyl, (C3-C4) branched alkyl, phenyl, or substituted phenyl, and optionally substituted with (C1-C4) alkyl, (C2-C4) alkenyl or -alkynyl, (C3-C7 ) branched alkyl, (C3-C7 ) cycloalkyl or -cycloalkenyl, halo, hydroxy, or acetyl, and Z is (a) a C1-C12 saturated or unsaturated hydro-carbon chain, straight chain or branched optionally in-cluding a hetero atom selected from O, S, SO, SO2, NR3, or SiR19R20, and optionally substituted with halo, halo (C1-C4) alkoxy, hydroxy, (C3-C8) cycloalkyl or cyclo-alkenyl, or (C1-C4) acyl; (b) (C3-C8) cycloalkyl or -cycloalkenyl, option-ally substituted with (C1-C4) alkyl, (C1-C4) alkoxy, halo (C1-C4) alkyl, halo (C1-C4) alkoxy, halo, hydroxy, or (C1-C4 ) acyl; (c) a phenyl group of the formula (2) (2) where R6 to R10 are independently H, halo, I, (C1-C10) alkyl, (C3-C8) alkenyl or -alkynyl, branched (C3-C6) alkyl, -alkenyl, or -alkynyl, (C3-C8) cycloalkyl or -cycloalkenyl, halo (C1-C7) alkyl, (C1-C7) alkoxy, (C1-C7) alkylthio, halo (C1-C7) alkoxy, phenoxy, substituted phenoxy, phenyl-thio, substituted phenylthio, phenyl, substituted phenyl, NO2, acetoxy, OH, CN, SiR11R12R13, OSiR11R12R13 NR14R15 S(O)R16, or SO2R17 where R11, R12, and R13 are independ-ently (C1-C4) alkyl, (C3-C4 ) branched alkyl, phenyl, or substituted phenyl, R1-4 and R1-5 are independently H, (C1-C4) alkyl, or (C1-C4) acyl, and R16 and R17 are phenyl, substituted phenyl, or (C1-C4 ) alkyl; (d) a furyl group of formula (3) (3) where R18 is H, halo, halomethyl, CN, NO2, (C1-C4) alkyl, (C3-C4 ) branched alkyl, phenyl, substituted phenyl, or (C1-C4) alkoxy; (e) a thienyl group of the formula (4) (4) where R18 is as defined in paragraph (d); (f) a group of formula (5) or (6) (6) (5) where R18 is as defined in paragraph (d), J is N or CH, and G is 0, NR19, or S, provided that if J is not N then G is NR19, where R19 is H, (C1-C4) alkyl, (C1-C4) acyl, phenylsulfonyl, or substituted phenylsulfonyl; (g) a group selected from optionally substituted naphthyl, dihydro-naphthyl, tetrahydronaphthyl, and decahydronaphthyl; optionally substituted pyridyl; optionally substituted indolyl; and 1,3-benzodioxolyl; or an acid addition salt or N-oxide of a compound of formula (1); are plant fungicides, miticides, and insecticides. |
| priorityDate | 1989-07-27^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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