ES2575987T3 - Nuevos derivados de N-fenetilcarboxamida - Google Patents
Nuevos derivados de N-fenetilcarboxamida Download PDFInfo
- Publication number
- ES2575987T3 ES2575987T3 ES06830070.6T ES06830070T ES2575987T3 ES 2575987 T3 ES2575987 T3 ES 2575987T3 ES 06830070 T ES06830070 T ES 06830070T ES 2575987 T3 ES2575987 T3 ES 2575987T3
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- Prior art keywords
- halogen atoms
- group
- alkyl
- halogen
- atoms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- NOOOMJZHMKSKBF-UHFFFAOYSA-N n-(2-phenylethyl)formamide Chemical class O=CNCCC1=CC=CC=C1 NOOOMJZHMKSKBF-UHFFFAOYSA-N 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 abstract description 90
- -1 pentafluoro-λ6-sulfanyl group Chemical group 0.000 abstract description 43
- 150000001875 compounds Chemical class 0.000 abstract description 37
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 24
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 19
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 14
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 13
- 125000004414 alkyl thio group Chemical group 0.000 abstract description 9
- 125000004438 haloalkoxy group Chemical group 0.000 abstract description 8
- 150000003839 salts Chemical class 0.000 abstract description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 7
- 125000003282 alkyl amino group Chemical group 0.000 abstract description 5
- 125000003277 amino group Chemical group 0.000 abstract description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract description 5
- 229910052736 halogen Inorganic materials 0.000 abstract description 3
- 125000004429 atom Chemical group 0.000 abstract description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract description 2
- 150000002367 halogens Chemical class 0.000 abstract description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 11
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 3
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 3
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 3
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 3
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 abstract 3
- 125000005292 haloalkynyloxy group Chemical group 0.000 abstract 3
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 2
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 abstract 2
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000004647 alkyl sulfenyl group Chemical group 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005202 dialkylaminocarbonyloxy group Chemical group 0.000 abstract 2
- 125000005117 dialkylcarbamoyl group Chemical group 0.000 abstract 2
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 abstract 2
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 abstract 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000000676 alkoxyimino group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 239000002184 metal Chemical class 0.000 abstract 1
- 229910052752 metalloid Inorganic materials 0.000 abstract 1
- 150000002738 metalloids Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 30
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 26
- 239000000203 mixture Substances 0.000 description 25
- 201000010099 disease Diseases 0.000 description 15
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 15
- 102100038019 Corticotropin-releasing factor receptor 2 Human genes 0.000 description 13
- 101000878664 Homo sapiens Corticotropin-releasing factor receptor 2 Proteins 0.000 description 13
- 241000196324 Embryophyta Species 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
- 230000002401 inhibitory effect Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 230000000855 fungicidal effect Effects 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 5
- 235000013399 edible fruits Nutrition 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000029058 respiratory gaseous exchange Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 3
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 3
- 241000233866 Fungi Species 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 2
- 241000208838 Asteraceae Species 0.000 description 2
- 241000219193 Brassicaceae Species 0.000 description 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 description 2
- 241000871189 Chenopodiaceae Species 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 description 2
- 241000440444 Phakopsora Species 0.000 description 2
- 239000005821 Propamocarb Substances 0.000 description 2
- 235000004789 Rosa xanthina Nutrition 0.000 description 2
- 241000220222 Rosaceae Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241000208292 Solanaceae Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- 229960003887 dichlorophen Drugs 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 229960002125 enilconazole Drugs 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 244000053095 fungal pathogen Species 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BLCKKNLGFULNRC-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;nickel(2+) Chemical compound [Ni+2].CN(C)C([S-])=S.CN(C)C([S-])=S BLCKKNLGFULNRC-UHFFFAOYSA-L 0.000 description 2
- 231100001184 nonphytotoxic Toxicity 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 2
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 2
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 2
- NTADARNNAPPIBY-UHFFFAOYSA-N triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1=CC=NC2=CN=NN12 NTADARNNAPPIBY-UHFFFAOYSA-N 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 1
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 description 1
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical class CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 description 1
- VPWGKZJMAGHQMR-OVVQPSECSA-N (2e)-2-[2-[6-(3-chloro-2-methylphenoxy)-5-fluoropyrimidin-4-yl]oxyphenyl]-2-methoxyimino-n-methylacetamide Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=NC=NC(OC=2C(=C(Cl)C=CC=2)C)=C1F VPWGKZJMAGHQMR-OVVQPSECSA-N 0.000 description 1
- URDNHJIVMYZFRT-KGLIPLIRSA-N (2r,3r)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan-3-ol Chemical compound C([C@H]([C@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-KGLIPLIRSA-N 0.000 description 1
- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 description 1
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical compound CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 description 1
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 description 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 description 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 1
- WRGKWWRFSUGDPX-UHFFFAOYSA-N 1-(4-chlorophenyl)-2-(1,2,4-triazol-1-yl)cycloheptan-1-ol Chemical compound C=1C=C(Cl)C=CC=1C1(O)CCCCCC1N1C=NC=N1 WRGKWWRFSUGDPX-UHFFFAOYSA-N 0.000 description 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 description 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 1
- ULCWZQJLFZEXCS-UHFFFAOYSA-N 1-[[2-(2,4-dichlorophenyl)-5-(2,2,2-trifluoroethoxy)oxolan-2-yl]methyl]-1,2,4-triazole Chemical compound O1C(OCC(F)(F)F)CCC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 ULCWZQJLFZEXCS-UHFFFAOYSA-N 0.000 description 1
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 description 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 1
- OKRROXQXGNEUSS-UHFFFAOYSA-N 1h-imidazol-1-ium-1-carboxylate Chemical compound OC(=O)N1C=CN=C1 OKRROXQXGNEUSS-UHFFFAOYSA-N 0.000 description 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 description 1
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 description 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 description 1
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 description 1
- NCDBYAPSWOPDRN-UHFFFAOYSA-N 2-[dichloro(fluoro)methyl]sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)F)C(=O)C2=C1 NCDBYAPSWOPDRN-UHFFFAOYSA-N 0.000 description 1
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- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 239000004560 ultra-low volume (ULV) liquid Substances 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 description 1
- 229960004740 voriconazole Drugs 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004565 water dispersible tablet Substances 0.000 description 1
- 239000004553 water soluble powder for seed treatment Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
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- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D327/06—Six-membered rings
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract
Un compuesto de fórmula general (I) de fórmula general (I)**Fórmula** en la que: - n es 1, 2, 3, 4 o 5; - p es 1, 2, 3, 4 o 5; - Xa es un átomo de halógeno, un grupo nitro, un grupo ciano, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-λ6-sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carbamoílo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino) alquilo C1-C6, un alquilo C1-C8, un halogenoalquilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquenilo C2-C8, un alquinilo C2-C8, un alquilamino C1-C8, un dialquilamino C1-C8, un alcoxi C1-C8, un halogenoalcoxi C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfanilo C1-C8, un halogenoalquilsulfanilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alqueniloxi C2-C8, un halogenoalqueniloxi C2-C8 que tiene de 1 a 5 átomos de halógeno, un alquiniloxi C3-C8, un halogenoalquiniloxi C3-C8 que tiene de 1 a 5 átomos de halógeno, un cicloalquilo C3-C8, un halogenocicloalquilo C3-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarbonilo C1-C8, un halogenoalquilcarbonilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarbamoílo C1-C8, un dialquilcarbamoílo C1-C8, un Nalquiloxicarbamoílo C1-C8, un alcoxicarbamoílo C1-C8, un N-alquil C1-C8 alcoxicarbamoílo C1-C8, un alcoxicarbonilo C1-C8, un halogenoalcoxicarbonilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarboniloxi C1-C8, un halogenoalquilcarboniloxi C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarbonilamino C1-C8, un halogenoalquilcarbonilamino C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilaminocarboniloxi C1-C8, un dialquilaminocarboniloxi C1-C8, un alquiloxicarboniloxi C1-C8, un alquilsulfenilo C1-C8, un halogenoalquilsulfenilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfinilo C1-C8, un halogenoalquilsulfinilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfonilo C1-C8, un halogenoalquilsulfonilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un (alcoxiimino C1-C6) alquilo C1-C6, un (alqueniloxiimino C1-C6) alquilo C1-C6, un (alquiniloxiimino C1-C6) alquilo C1-C6 o un (benciloxiimino) alquilo C1-C6; - X es igual o diferente y es un átomo de hidrógeno, un átomo de halógeno, un grupo nitro, un grupo ciano, un grupo amino, un grupo sulfanilo, un grupo pentafluoro-λ 6-sulfanilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carbamoílo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino) alquilo C1-C6, un alquilo C1-C8, un halogenoalquilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquenilo C2- C8, un alquinilo C2-C8, un alquilamino C1-C8, un dialquilamino C1-C8, un alcoxi C1-C8, un halogenoalcoxi C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfanilo C1-C8, un halogenoalquilsulfanilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alqueniloxi C2-C8, un halogenoalqueniloxi C2-C8 que tiene de 1 a 5 átomos de halógeno, un alquiniloxi C3-C8, un halogenoalquiniloxi C3-C8 que tiene de 1 a 5 átomos de halógeno, un cicloalquilo C3-C8, un halogenocicloalquilo C3-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarbonilo C1- C8, un halogenoalquilcarbonilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarbamoílo C1-C8, un dialquilcarbamoílo C1-C8, un N-alquiloxicarbamoílo C1-C8, un alcoxicarbamoílo C1-C8, un N-alquil C1-C8 alcoxicarbamoílo C1-C8, un alcoxicarbonilo C1-C8, un halogenoalcoxicarbonilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilcarboniloxi C1-C8, un halogenoalquilcarboniloxi C1-C3 que tiene de 1 a 5 átomos de halógeno, un alquilcarbonilamino C1-C8, un halogenoalquilcarbonilamino C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilaminocarboniloxi C1-C8, un dialquilaminocarboniloxi C1-C8, un alquiloxicarboniloxi C1-C8, un alquilsulfenilo C1-C8, un halogenoalquilsulfenilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfinilo C1-C8, un halogenoalquilsulfinilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfonilo C1-C8, un halogenoalquilsulfonilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un (alcoxiimino C1-C6) alquilo C1-C6, un (alqueniloxiimino C1-C6) alquilo C1-C6, un (alquiniloxiimino C1-C6) alquilo C1-C6 o un (benciloxiimino) alquilo C1-C6; - R1 es un átomo de hidrógeno, un alquilo C1-C6, o un cicloalquilo C3-C7; - Het representa heterociclo de 5, 6 o 7 miembros con uno, dos o tres heteroátomos que pueden ser iguales o diferentes; estando unido Het mediante un átomo de carbono; - Ya es un sustituyente en orto y es un átomo de halógeno, un grupo ciano, un grupo sulfanilo, un grupo pentafluoro-λ 6-sulfanilo, un grupo formilo, un alquilo C1-C8, un halogenoalquilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquenilo C2-C8, un alquinilo C2-C8, un alcoxi C1-C8, un halogenoalcoxi C1-C8 que tiene de 1 a 5 átomos de halógeno, un alquilsulfanilo C1-C8, un halogenoalquilsulfanilo C1-C8 que tiene de 1 a 5 átomos de halógeno, un alqueniloxi C2-C8, un halogenoalqueniloxi C2-C8 que tiene de 1 a 5 átomos de halógeno, un alquiniloxi C3-C8, un halogenoalquiniloxi C3-C8 que tiene de 1 a 5 átomos de halógeno, un cicloalquilo C3-C8 o un halogenocicloalquilo C3-C8 que tiene de 1 a 5 átomos de halógeno; y - Y es un átomo de hidrógeno, un átomo de halógeno, un grupo amino, un alquilamino C1-C8, un dialquilamino C1-C8, un alquilo C1-C6 o un halogenoalquilo C1-C6; así como sus sales, N-óxidos, complejos metálicos, complejos metaloides e isómeros ópticamente activos; con la condición de que el compuesto de fórmula general (I) es diferente de: - 5-cloro-N-[2-(2-fluorofenil)etil]-1-metil-1H-pirazol-4-carboxamida; - 5-cloro-N-[2-(2,4-diclorofenil)etil]-1-metil-1H-pirazol-4-carboxamida y - 1-metil-5 N-[2-(2,3,4-tribromo-5-metoxifenil)etil]-L-prolinamida.
Description
en la que:
R28
-puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo amino, un grupo ciano, un alquilamino C1-C4, un di(alquil C1-C4)amino, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno o un fenilo opcionalmente sustituido con un átomo de halógeno o un alquilo C1-C4; y
-R29 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno.
* Het representa un heterociclo de fórmula general (Het-11)
10 en la que:
R30
-puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo amino, un grupo ciano, un alquilamino C1-C4, un di(alquil C1-C4)amino, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno; y
-R31 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos 15 de halógeno.
* Het representa un heterociclo de fórmula general (Het-12)
en la que:
-R32 puede ser un átomo de halógeno, un grupo ciano, un grupo nitro, un alquilo C1-C4, un halogenoalquilo C1
20 C4 que tiene de 1 a 5 átomos de halógeno, un cicloalquilo C3-C6, un alcoxi C1-C4, un halogenoalcoxi C1-C4 que tiene de 1 a 5 átomos de halógeno, un alquiltio C1-C4, un halogenoalquiltio C1-C4 que tiene de 1 a 5 átomos de halógeno, un grupo aminocarbonilo o un aminocarbonil-alquilo C1-C4; -R33 puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo nitro, un alquilo C1-C4, un alcoxi C1-C4 o un alquiltio C1-C4; y
25 -R34 puede ser un átomo de hidrógeno, un fenilo, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un hidroxialquilo C1-C4, un alquenilo C2-C6, un cicloalquilo C3-C6, un alquiltio C1-C4 alquilo C1-C4, un halogenoalquiltio C1-C4 alquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un alcoxi C1-C4 alquilo C1-C4 o un halogenoalcoxi C1-C4 alquilo C1-C4 que tiene de 1 a 5 átomos de halógeno.
* Het representa un heterociclo de fórmula general (Het-13)
en la que:
-R35 puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo nitro, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un cicloalquilo C3-C6, un alcoxi C1-C4, un halogenoalcoxi C1-C4 que tiene de 1 a 5 átomos de halógeno, un alquiltio C1-C4, un halogenoalquiltio C1
C4 que tiene de 1 a 5 átomos de halógeno, un aminocarbonilo o un aminocarbonil-alquilo C1-C4;
-R36 puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un alquilo C1-C4, un alcoxi C1-C4, un halogenoalcoxi C1-C4 que tiene de 1 a 5 átomos de halógeno o un alquiltio C1-C4; y
-R37 puede ser un átomo de hidrógeno, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos
5 de halógeno, un hidroxialquilo C1-C4, un alquenilo C2-C6, un cicloalquilo C3-C6, un alquiltio C1-C4 alquilo C1-C4, un halogenoalquiltio C1-C4 alquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un alcoxi C1-C4 alquilo C1-C4, un halogenoalcoxi C1-C4 alquilo C1-C4 que tiene de 1 a 5 átomos de halógeno o un fenilo opcionalmente sustituido con un átomo de halógeno, un alquilo C1-C4, un alcoxialquilo C1-C4 o un grupo nitro; con la condición de que R35 y R36 no sean ambos un átomo de hidrógeno.
10 * Het representa un heterociclo de fórmula general (Het-14)
en la que:
-R38 puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo nitro, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un cicloalquilo C3-C6, un alcoxi C1-C4, 15 un halogenoalcoxi C1-C4 que tiene de 1 a 5 átomos de halógeno, un alquiltio C1-C4, un halogenoalquiltio C1-
C4 que tiene de 1 a 5 átomos de halógeno, un aminocarbonilo, o un aminocarbonil-alquilo C1-C4;
-R39 puede ser un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un alquilo C1-C4, un alcoxi C1-C4, un alquiltio C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno;
-R40 puede ser un átomo de hidrógeno, un fenilo, un bencilo, un alquilo C1-C4, un halogenoalquilo C1-C4 que
20 tiene de 1 a 5 átomos de halógeno, un hidroxialquilo C1-C4, un alquenilo C2-C6, un cicloalquilo C3-C6, un alquiltio C1-C4 alquilo C1-C4, un halogenoalquiltio C1-C4 alquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un alcoxi C1-C4 alquilo C1-C4, un halogenoalcoxi C1-C4 alquilo C1-C4 que tiene de 1 a 5 átomos de halógeno; con la condición de que R39 y R40 no sean ambos un átomo de hidrógeno.
* Het representa un heterociclo de fórmula general (Het-15)
25
en la que:
-R41 puede ser un átomo de hidrógeno, un átomo de halógeno, un alquilo C-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno; y -R42 puede ser un átomo de halógeno, un alquilo C-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos 30 de halógeno.
* Het representa un heterociclo de fórmula general (Het-16)
en la que R43 y R44 pueden ser iguales o diferentes y pueden ser un átomo de hidrógeno, un átomo de halógeno, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, un fenilo opcionalmente sustituido con un átomo de halógeno o un alquilo C1-C4, o un heterociclilo opcionalmente sustituido con un átomo de halógeno o un alquilo C1-C4; con la condición de que R43 y R44 no sean ambos un átomo de hidrógeno.
* Het representa un heterociclo de fórmula general (Het-17)
en la que
-R44 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, y
-R45 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno.
* Het representa un heterociclo de fórmula general (Het-18)
en la que R46 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno.
* Het representa un heterociclo de fórmula general (Het-19)
en la que:
-R48 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno; y
-R49 puede ser un átomo de hidrógeno, un alquilo C1-C4, un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno, o un fenilo opcionalmente sustituido con un átomo de halógeno o un alquilo C1-C4.
* Het representa un heterociclo de fórmula general (Het-20)
20 en la que R50 puede ser un átomo de halógeno, un alquilo C1-C4 o un halogenoalquilo C1-C4 que tiene de 1 a 5 átomos de halógeno.
De acuerdo con la presente invención, "Het" del compuesto de fórmula general (I) puede ser un heterociclo de anillo de seis miembros. Algunos ejemplos específicos los de compuestos de la presente invención donde Het es un heterociclo de seis miembros incluyen:
25 * Het representa un heterociclo de fórmula general (Het-21)
en la que: -R51 puede ser un átomo de halógeno, un grupo hidroxi, un grupo ciano, un alquilo C1-C4, un halogenoalquilo
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proporcionar un compuesto de fórmula general (Ia).
El compuesto de acuerdo con la presente invención se puede preparar de acuerdo con los procedimientos generales de preparación descritos anteriormente. No obstante, se ha de entender que, en base a su conocimiento general y a las publicaciones disponibles, el experto será capaz de adaptar este procedimiento de acuerdo con las especificaciones de cada uno de los compuestos que se desea sintetizar.
En base a su conocimiento general y a las publicaciones disponibles, el experto también será capaz de preparar el compuesto intermedio de fórmula (V) de acuerdo con la presente invención.
La presente invención también se refiere a una composición fungicida que comprende una cantidad eficaz de un principio activo de fórmula general (I). De ese modo, de acuerdo con la presente invención, se proporciona una composición fungicida que comprende, como principio activo, una cantidad eficaz de un compuesto de fórmula general (I) como se ha definido anteriormente y un soporte, vehículo o carga agrícolamente aceptable.
En la presente memoria descriptiva, el término "soporte" representa un material natural o sintético, orgánico o inorgánico con el que se combina el principio activo para hacerlo más fácil de aplicar, especialmente en las partes de la planta. De ese modo, este soporte es generalmente inerte y debería ser agrícolamente aceptable. El soporte puede ser un sólido o un líquido. Algunos ejemplos de soportes adecuados incluyen arcillas, silicatos naturales o sintéticos, sílice, resinas, ceras, fertilizantes sólidos, agua, alcoholes, en particular butanol, disolventes orgánicos, aceites minerales y de plantas y derivados de los mismos. También se pueden usar mezclas de tales soportes.
La composición también puede comprender componentes adicionales. En particular, la composición puede comprender además un tensioactivo. El tensioactivo puede ser un emulgente, un agente de dispersión o un agente humectante de tipo iónico o no iónico o una mezcla de tales tensioactivos. Se puede hacer mención, por ejemplo, a sales de ácidos poliacrílicos, sales de ácido lignosulfónico, sales de ácido fenolsulfónico o naftalenosulfónico, policondensados de óxido de etileno con alcoholes grasos o con ácidos grasos o con aminas grasas, fenoles sustituidos (en particular alquilfenoles o arilfenoles), sales de ésteres del ácido sulfosuccínico, derivados de taurina (en particular tauratos de alquilo), ésteres fosfóricos de alcoholes o fenoles polioxietilados, ésteres de ácidos grasos de polioles, y derivados de los compuestos anteriores que contienen funcionalidades sulfato, sulfonato y fosfato. La presencia de al menos un tensioactivo es generalmente esencial cuando el principio activo y/o el soporte inerte son insolubles en agua y cuando el agente vector para la aplicación es agua. Preferentemente, el contenido de tensioactivo puede estar comprendido entre un 5 % y 40 % en peso de la composición.
Opcionalmente, también se pueden incluir componentes adicionales, por ejemplo coloides protectores, adhesivos, espesantes, agentes tixotrópicos, agentes de penetración, estabilizadores, agentes secuestrantes. Más generalmente, se pueden combinar los materiales activos con cualquier aditivo sólido o líquido, que cumpla con las técnicas de formulación habituales.
En general, la composición de acuerdo con la invención puede contener de un 0,05 a un 99 % (en peso) de principio activo, preferentemente de un 10 a un 70 % en peso.
Las composiciones de acuerdo con la presente invención se pueden usar en diversas formas tales como dispensador de aerosol, suspensión de cápsula, concentrado de nebulización en frío, polvo humedecible, concentrado emulsionable, emulsión de aceite en agua, emulsión de agua en aceite, gránulo encapsulado, gránulo fino, concentrado fluido para tratamiento de semillas, gas (a presión), producto generador de gas, gránulo, concentrado de nebulización en caliente, macrogránulo, microgránulo, polvo dispersable en aceite, concentrado fluido miscible en aceite, líquido miscible en aceite, pasta, barrita para plantas, polvo para tratamiento de semillas en seco, semilla revestida con un pesticida, concentrado soluble, polvo soluble, solución para tratamiento de semillas, concentrado en suspensión (concentrado fluido), líquido de ultra bajo volumen (ulv), suspensión de ultra bajo volumen (ulv), gránulos o comprimidos dispersables en agua, polvo dispersable en agua para tratamiento en suspensión, gránulos o comprimidos solubles en agua, polvo soluble en agua para el tratamiento de semillas, y polvo humectable.
Estas composiciones incluyen no solo composiciones que están listas para aplicarse a la planta o semilla que se trata por medio de un dispositivo adecuado, tal como un dispositivo de pulverización o espolvoreado, sino también composiciones comerciales concentradas que se deben diluir antes de la aplicación al cultivo.
Los compuestos de la invención también se pueden mezclar con uno o más insecticidas, fungicidas, bactericidas, acaricias o feromonas atractoras u otros compuestos con actividad biológica. Las mezclas obtenidas de ese modo tienen un espectro ampliado de actividad. Las mezclas con otros fungicidas son particularmente ventajosas. Algunos ejemplos de acompañantes de mezcla de fungicidas apropiados se pueden seleccionar entre las siguientes listas:
1) un compuesto capaz de inhibir la síntesis de ácidos nucleicos tal como benalaxilo, benalaxilo-M, bupirimato, ciralaxilo, clozilacón, dimetirimol, etirimol, furalaxilo, himexazol, mefenoxam, metalaxilo, metalaxilo-M, ofurace, oxadixilo y ácido oxolínico; 2) un compuesto capaz de inhibir la mitosis y la división celular tal como benomilo, carbendazim, dietofencarb, etaboxam, fuberidazol, pencicurón, tiabendazol tiofanato-metilo, zoxamida;
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3) un compuesto capaz de inhibir la respiración, por ejemplo como inhibidor de la respiración de CI tal como diflumetorim; como inhibidor de la respiración de CII tal como boscalid, carboxina, fenfuram, flutolanilo, furametpir, furmeciclox, mepronilo, oxicarboxina, pentiopirad, tifluzamida; como inhibidor de la respiración de CIII tal como amisulbrom, azoxistrobina, ciazofamid, dimoxistrobina, enestrobina, famoxadona, fenamidona, fluoxastrobina, kresoxim-metilo, metominostrobina, orisastrobina, picoxistrobina, piraclostrobina, trifloxistrobina; 4) un compuesto capaz de actuar como un desacoplador tal como dinocap, fluazinam, meptildinocap; 5) un compuesto capaz de inhibir la producción de ATP tal como acetato de fentina, cloruro de fentina, hidróxido de fentina, siltiofam; 6) un compuesto capaz de inhibir la biosíntesis de AA y de proteínas tal como andoprim, blasticidina-S, ciprodinilo, kasugamicina, hidrato de clorhidrato de kasugamicina, mepanipirim, pirimetanilo; 7) un compuesto capaz de inhibir la transducción de señal tal como fenpiclonilo, fludioxonilo, quinoxifen; 8) un compuesto capaz de inhibir la síntesis de lípidos y de membranas tal como bifenilo, clozolinato, edifenfós, etridiazol, iodocarb, iprobenfós, iprodiona, isoprotiolano, procimidona, propamocarb, clorhidrato de propamocarb, pirazofós, tolclofós-metilo, vinclozolina; 9) un compuesto capaz de inhibir la biosíntesis de ergosterol tal como aldimorf, azaconazol, bitertanol, bromuconazol, ciproconazol, diclobutrazol, difenoconazol, diniconazol, diniconazol-M, dodemorf, acetato de dodemorf, epoxiconazol, etaconazol, fenarimol, fenbuconazol, fenhexamid, fenpropidina, fenpropimorf, fluquinconazol, flurprimidol, flusilazol, flutriafol, furconazol, furconazol-cis, hexaconazol, imazalilo, sulfato de imazalilo, imibenconazol, ipconazol, metconazol, miclobutanilo, naftifina, nuarimol, oxpoconazol, paclobutrazol, pefurazoato, penconazol, procloraz, propiconazol, protioconazol, piributicarb, pirifenox, simeconazol, espiroxamina, tebuconazol, terbinafina, tetraconazol, triadimefón, triadimenol, tridemorf, triflumizol, triforina, triticonazol, uniconazol, viniconazol, voriconazol; 10) un compuesto capaz de inhibir la síntesis de la pared celular tal como bentiavalicarb, bialafós, dimetomorf, flumorf, iprovalicarb, mandipropamid, polioxinas, polioxorim, validamicina A; 11) un compuesto capaz de inhibir biosíntesis de melanina tal como carpropamid, diclocimet, fenoxanilo, ftalida, piroquilona, triciclazol; 12) un compuesto capaz de inducir la defensa del hospedador tal como acibenzolar-S-metilo, probenazol, tiadinilo; 13) un compuesto capaz de tener una acción en múltiples sitios tal como mezcla de burdeos, captafol, captán, clorotalonilo, naftenato de cobre, óxido de cobre, oxicloruro de cobre, preparaciones de cobre tales como hidróxido de cobre, sulfato de cobre, diclofluanid, ditianona, dodina, base libre de dodina, ferbam, fluorofolpet, folpet, guazatina, acetato de guazatina, iminoctadina, albesilato de iminoctadina, triacetato de iminoctadina, mancobre, mancozeb, maneb, metiram, metiram cinc, oxina-cobre, propineb, azufre y preparaciones de azufre incluyendo polisulfuro de calcio, tiram, tolilfluanid, zineb, ziram; 14) un compuesto seleccionado entre la siguiente lista: (2E)-2-(2-{[6-(3-cloro-2-metilfenoxi)-5-fluoropirimidin-4il]oxi}fenil)-2-(metoxiimino)-N-metilacetamida, (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2fenilvinil]oxi}fenil)etilideno]amino}oxi)metil]fenil}-2-(metoxiimino)-N-metilacetamida, 1-(4-clorofenil)-2-(1H-1,2,4triazol-1-il)cicloheptanol, 1H-imidazol-1-carboxilato de 1-[(4-metoxifenoxi)metil]-2,2-dimetilpropilo, 2,3,5,6tetracloro-4-(metilsulfonil)piridina, 2-butoxi-6-yodo-3-propil-4H-cromen-4-ona, 2-cloro-N-(1,1,3-trimetil-2,3-dihidro1H-inden-4-il)nicotinamida, 2-fenilfenol y sales, 3,4,5-tricloropiridin-2,6-dicarbonitrilo, 3,4-dicloro-N-(2cianofenil)isotiazol-5-carboxamida, 3-[5-(4-clorofenil)-2,3-dimetilisoxazolidin-3-il]piridina, 5-cloro-6-(2,4,6trifluorofenil)-N-[(1R)-1,2,2-trimetilpropil][1.2.4]triazolo[1,5-a]pirimidin-7-amina, 5-cloro-7-(4-metilpiperidin-1-il)-6(2,4,6-trifluorofenil)[1.2.4]triazolo[1,5-a]pirimidina, 5-cloro-N-[(1R)-1,2-dimetilpropil]-6-(2,4,6trifluorofenil)[1.2.4]triazolo[1,5-a]pirimidin-7-amina, sulfato de 8-hidroxiquinolina, bentiazol, betoxazina, capsimicina, carvona, quinometionato, cufraneb, ciflufenamid, cimoxanilo, dazomet, debacarb, diclorofeno, diclomezina, diclorano, difenzoquat, metilsulfato de difenzoquat, difenilamina, ferimzona, flumetover, fluopicolida, fluoroimida, flusulfamida, fosetil-aluminio, fosetil-calcio, fosetil-sodio, hexaclorobenceno, irumamicina, isotianilo, metasulfocarb, (2E)-2-{2-[({ciclopropil[(4-metoxifenil)imino]metil}tio)metil]fenil}-3-metoxiacrilato de metilo, 1-(2,2dimetil-2,3-dihidro-1H-inden-1-il)-1H-imidazol-5-carboxilato de metilo, isotiocianato de metilo, metrafenona, mildiomicina, N-(3',4'-dicloro-5-fluorobifenil-2-il)-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida, N-(3-etil-3,5,5trimetilciclohexil)-3-(formilamino)-2-hidroxibenzamida, N-(4-cloro-2-nitrofenil)-N-etil-4-metilbencenosulfonamida, N-(4-clorobencil)-3-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]propanamida, N-[(4-clorofenil)(ciano)metil]-3-[3-metoxi-4(prop-2-in-1-iloxi)fenil]propanamida, N-[(5-bromo-3-cloropiridin-2-il)metil]-2,4-dicloronicotinamida, N-[1-(5-bromo3-cloropiridin-2-il)etil]-2,4-dicloronicotinamida, N-[1-(5-bromo-3-cloropiridin-2-il)etil]-2-fluoro-4-yodonicotinamida, N-[2-(4-{[3-(4-clorofenil)prop-2-in-1-il]oxi}-3-metoxifenil)etil]-N-(metilsulfonil)valinamida, N-{(Z)[(ciclopropilmetoxi)imino][6-(difluorometoxi)-2,3-difluorofenil]metil}-2-fenilacetamida, N-{2-[1,1'-bi(ciclopropil)-2il]fenil}-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida, N-{2-[3-cloro-5-(trifluorometil)piridin-2-il]etil}-2(trifluorometil)benzamida, natamicina, N-etil-N-metil-N'-{2-metil-5-(trifluorometil)-4-[3(trimetilsilil)propoxi]fenil}imidoformamida, N-etil-N-metil-N'-{2-metil-5-(difluorometil)-4-[3(trimetilsilil)propoxi]fenil}imidoformamida, dimetilditiocarbamato de níquel, nitrotal-isopropilo, 1H-imidazol-1carbotioato de O-{1-[(4-metoxifenoxi)metil]-2,2-dimetilpropilo}, octilinona, oxamocarb, oxifentiina, pentaclorofenol y sales, ácido fosforoso y sus sales, piperalina, fosetilato de propamocarb, propanosina-sodio, proquinazid, piribencarb, pirrolnitrina, quintozeno, tecloftalam, tecnazeno, triazóxido, triclamida, valifenal, zarilamid.
La composición de acuerdo con la invención que comprende una mezcla de un compuesto de fórmula (I) con un compuesto bactericida también puede ser particularmente ventajosa. Algunos ejemplos de acompañantes de mezcla de bactericidas adecuados se puede seleccionar en la siguiente lista: bronopol, diclorofeno, nitrapirina, dimetilditiocarbamato de níquel, kasugamicina, octilinona, ácido furanocarboxílico, oxitetraciclina, probenazol,
5 estreptomicina, tecloftalam, sulfato de cobre y otras preparaciones de cobre.
Las composiciones fungicidas de la presente invención se pueden usar para controlar de forma curativa o preventiva los hongos fitopatógenos de los cultivos. De ese modo, de acuerdo con un aspecto adicional de la presente invención, se proporciona un procedimiento para controlar de forma curativa o preventiva los hongos fitopatógenos de cultivos caracterizado porque se aplica una composición fungicida como se ha indicado anteriormente en el
10 presente documento a la semilla, la planta y/o a la fruta de la planta o al suelo en el que crece la planta o en el que se desea que crezca.
La composición que se usa frente a hongos fitopatógenos de cultivos comprende una cantidad eficaz y no fitotóxica de un principio activo de fórmula general (I).
La expresión "cantidad eficaz y no fitotóxica" significa una cantidad de una composición de acuerdo con la invención
15 que es suficiente para controlar o destruir los hongos presentes o que puedan aparecer en los cultivos, y que no supone ningún síntoma apreciable de fitotoxicidad para dichos cultivos. Tal cantidad puede variar dentro de un amplio intervalo dependiendo de los hongos que se van a controlar, el tipo de cultivo, las condiciones climáticas y los compuestos incluidos en la composición fungicida de acuerdo con la invención.
Esta cantidad se puede determinar mediante ensayos de campo sistemáticos, que están dentro de las capacidades 20 del experto en la materia.
El procedimiento de tratamiento de acuerdo con la presente invención es útil para tratar material de propagación tal como tubérculos o rizomas, pero también semillas, plantones o trasplante de plantones y plantas o trasplante de plantas. Este procedimiento de tratamiento también puede ser útil para tratar raíces. El procedimiento de tratamiento de acuerdo con la presente invención también puede ser útil para tratar las partes de superficie de la planta tales
25 como troncos, tallos o pedúnculos, hojas, flores y frutos de la correspondiente planta.
Entre las plantas que se pueden proteger mediante el procedimiento de acuerdo con la presente invención, se puede hacer mención a algodón; lino; parra; cultivos de frutas u hortalizas tales como Rosaceae sp. (por ejemplo frutas con pipas, tales como manzanas y peras, pero también frutas con hueso, tales como albaricoques, almendras y melocotones), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp.,
30 Oleaceae sp., Actinidaceae sp. Lauraceae sp., Musaceae sp. (por ejemplo árboles y plantaciones de plátanos), Rubiaceae sp., Theaceae sp., Sterculiceae sp., Rutaceae sp. (por ejemplo limones, naranjas y pomelo); Solanaceae sp. (por ejemplo tomates), Liliaceae sp., Asteraceae sp. (por ejemplo lechugas), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Papiliorraceae sp. (por ejemplo guisantes), Rosaceae sp. (por ejemplo fresas); cultivos principales tales como Graminae sp. (por ejemplo maíz, césped, cereales tales como trigo, arroz,
35 cebada y triticale), Asteraceae sp. (por ejemplo girasol), Cruciferae sp. (por ejemplo colza), Fabacae sp. (por ejemplo cacahuetes), Papilionaceae sp. (por ejemplo soja), Solanaceae sp. (por ejemplo patatas), Chenopodiaceae sp. (por ejemplo remolachas); cultivos de horticultura y forestales; así como homólogos genéticamente modificados de estos cultivos.
Entre las enfermedades de plantas o cultivos que se pueden controlar mediante el procedimiento de acuerdo con la 40 presente invención, se puede hacer mención a:
Enfermedades del mildiú pulverulento, tales como:
enfermedades producidas por Blumeria, causadas, por ejemplo, por Blumeria graminis; enfermedades producidas por Podosphaera, causadas, por ejemplo, por Podosphaera leucotricha; enfermedades producidas por Sphaerotheca, causadas, por ejemplo, por Sphaerotheca fuliginea;
45 enfermedades producidas por Uncinula, causadas, por ejemplo, por Uncinula necator;
Enfermedades de la roya, tales como:
enfermedades producidas por Gymnosporangium, causadas, por ejemplo, por Gymnosporangium sabinae; enfermedades producidas por Hemileia, causadas, por ejemplo, por Hemileia vastatrix; enfermedades producidas por Phakopsora, causadas, por ejemplo, por Phakopsora pachyrhizi o Phakopsora
50 meibomiae; enfermedades producidas por Puccinia, causadas, por ejemplo, por Puccinia recondita; enfermedades producidas por Uromyces, causadas, por ejemplo, por Uromyces appendiculatus;
Enfermedades producidas por oomicetos, tales como:
enfermedades producidas por Bremia, causadas, por ejemplo, por Bremia lactucae; 55 enfermedades producidas por Peronospora, causadas, por ejemplo, por Peronospora pisi o P. brassicae;
Tabla A
- Compuesto
- R1 X1 X2 X3 X4 Xa Y1 Y2 Ya (M+1)
- A-1
- H H Cl H H Cl H H Br 378
- A-2
- H H Cl H H Cl H H Me 314
Tabla B
- Compuesto
- R1 X1 X2 X3 x4 xa Q Ya Y1 Y2 (M+1)
- B-1
- H H CF3 H Cl Cl S Me H H 400
Tabla C
- Compuesto
- R1 X1 X2 X3 X4 Xa Ya Y1 Y2 (M+1)
- C-1
- H H Cl H H Cl Me H H 298
Tabla D
- Compuesto
- R1 X1 X2 X3 X4 Xa Ya Y1 (M+1)
(continuación)
- Compuesto
- R1 X1 X2 X3 X4 Xa Ya Y1 (M+1)
- D-1
- H H H Me H Me CF3 Me 343
- D-2
- H H Me H H Me CF3 Me 343
- D-3
- H H H OMe H OMe CF3 Me 375
- D-4
- H H H H Cl Cl CF3 Me 383
- D-5
- H H H H H OMe CF3 Me 349
- D-6
- H H H H H Me CF3 Me 329
- D-7
- H H H H H Cl CF3 Me 349
- D-8
- H H Cl H H Cl Me NH2 330
- D-9
- H H Cl H H Cl CF3 Me 383
- D-10
- H H CF3 H Cl Cl CF3 Me 451
- D-11
- H OMe H H H OMe CF3 Me 375
- D-12
- H H Cl H H Cl CRF2 Me 365
Tabla E
- Compuesto
- R1 X1 X2 X3 X4 Xa Ya Y1 Y2 Y3 (M+1)
- E-1
- H H H Me H Me Cl H H H 289
- E-2
- H H H H H Me Cl H H H 275
- E-3
- H H Cl H H Cl Cl H H H 328
- E-4
- H H H H Cl Cl Cl H H H 329
- E-5
- H OMe H H H OMe Cl H H H 321
- E-6
- H H H H H OMe Cl H H H 291
- E-7
- H H H OMe H OMe Cl H H H 321
- E-8
- H H CF3 H Cl Cl Cl H H H 397
- E-9
- H H Me H H Me Cl H H H 289
- E-10
- H H H H H Cl Cl H H H 295
Tabla F
- Compuesto
- R1 X1 X2 X3 X4 Xa Ya Y1 Y2 Y3 (M+1)
- F-1
- H H Cl H H Cl CF3 H Me H 365
Tabla G
- Compuesto
- R1 X1 X2 X3 X4 Xa Ya Y1 Y2 (M+1)
- G-1
- H H Cl H H Cl CRF2 H Me 348
- G-2
- H H H H H Cl CRF2 H Me 314
- G-3
- H OMe H H H OMe CRF2 H Me 340
- G-4
- H H H H H OMe CRF2 H Me 310
- G-5
- H H Me H H Me CRF2 H Me 308
- G-6
- H H H H Cl Cl CRF2 H Me 348
- G-7
- H H H OMe H OMe CRF2 H Me 340
- G-8
- H H F H H F CRF2 H Me 316
- G-9
- H H H Me H Me CRF2 H Me 308
- G-10
- H H H Br H OMe CRF2 H Me 388
- G-11
- H H CF3 H Cl Cl CRF2 H Me 416
- G-12
- H H H H H Me CRF2 H Me 294
- G-13
- H OMe H H Br H CF3 H Me 406
- G-14
- H H H H H Me CF3 H Me 312
- G-15
- H H CF3 H H Cl CF3 H Me 400
- G-16
- H H H H H OMe CF3 H Me 328
- G-17
- H H H Me H Me CF3 H Me 326
- G-18
- H H H OMe H OMe CF3 H Me 358
- G-19
- H OMe H H H OMe CF3 H Me 358
- G-20
- H H F H H F CF3 H Me 334
- G-21
- H H H H Cl Cl CF3 H Me 366
Claims (1)
-
imagen1 imagen2 imagen3
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05356203 | 2005-11-22 | ||
| EP05356203A EP1787981A1 (en) | 2005-11-22 | 2005-11-22 | New N-phenethylcarboxamide derivatives |
| PCT/EP2006/068723 WO2007060166A1 (en) | 2005-11-22 | 2006-11-21 | New n-phenethylcarboxamide derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2575987T3 true ES2575987T3 (es) | 2016-07-04 |
Family
ID=35676257
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES06830070.6T Active ES2575987T3 (es) | 2005-11-22 | 2006-11-21 | Nuevos derivados de N-fenetilcarboxamida |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9440946B2 (es) |
| EP (2) | EP1787981A1 (es) |
| JP (1) | JP5363815B2 (es) |
| ES (1) | ES2575987T3 (es) |
| PL (1) | PL1954674T3 (es) |
| PT (1) | PT1954674E (es) |
| WO (1) | WO2007060166A1 (es) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI435863B (zh) | 2006-03-20 | 2014-05-01 | Nihon Nohyaku Co Ltd | N-2-(雜)芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑 |
| US20110207771A1 (en) * | 2006-06-08 | 2011-08-25 | Syngenta Crop Protection, Inc. | N-(l-alkyl-2-phenylethyl)-carboxamide derivatives and use thereof as fungicides |
| CL2008001647A1 (es) | 2007-06-08 | 2008-10-10 | Syngenta Participations Ag | Compuestos derivados de feniletil-amida de acido-1h-pirazol-4-carboxilico; compuestos derivados de (feniletil)amina; metodo para controlar o prevenir la infestacion de plantas por parte de microorganismos fitopatogenos; y composicion para el control |
| US10793515B2 (en) | 2008-03-19 | 2020-10-06 | Aurimmed Pharma, Inc. | Compounds advantageous in the treatment of central nervous system diseases and disorders |
| WO2009117515A2 (en) | 2008-03-19 | 2009-09-24 | Aurimmed Pharma, Inc. | Novel compounds advantageous in the treatment of central nervous system diseases and disorders |
| US9212155B2 (en) | 2008-03-19 | 2015-12-15 | Aurimmed Pharma, Inc. | Compounds advantageous in the treatment of central nervous system diseases and disorders |
| US20210130285A1 (en) | 2008-03-19 | 2021-05-06 | Aurimmed Pharma, Inc. | Novel compounds advantageous in the treatment of central nervous system diseases and disorders |
| GB0807139D0 (en) * | 2008-04-18 | 2008-05-21 | Syngenta Participations Ag | Novel microbiocides |
| GB0807140D0 (en) * | 2008-04-18 | 2008-05-21 | Syngenta Participations Ag | Novel microbiocides |
| GB0807138D0 (en) * | 2008-04-18 | 2008-05-21 | Syngenta Participations Ag | Novel microbiocides |
| CA2731200A1 (en) | 2008-08-01 | 2010-02-04 | Bayer Cropscience Ag | Fungicidal n-(2-phenoxyethyl)carboxamide derivatives and their aza, thia and sila analogues |
| AU2009324187B2 (en) * | 2008-12-05 | 2014-07-31 | Syngenta Crop Protection Ag | Novel pyrazole-4 -N-alkoxycarboxamides as microbiocides |
| EP2218717A1 (en) * | 2009-02-17 | 2010-08-18 | Bayer CropScience AG | Fungicidal N-((HET)Arylethyl)thiocarboxamide derivatives |
| JP2010270031A (ja) * | 2009-05-20 | 2010-12-02 | Sumitomo Chemical Co Ltd | アミド化合物とその植物病害防除用途 |
| SG176983A1 (en) | 2009-07-08 | 2012-02-28 | Dermira Canada Inc | Tofa analogs useful in treating dermatological disorders or conditions |
| ES2470148T3 (es) | 2010-05-28 | 2014-06-23 | Syngenta Participations Ag | Derivados de pirazolocarboxamida y su uso como microbiocidas |
| WO2011151369A1 (en) | 2010-06-03 | 2011-12-08 | Bayer Cropscience Ag | N-[(het)arylethyl)] pyrazole(thio)carboxamides and their heterosubstituted analogues |
| BR112014012589A2 (pt) * | 2011-11-25 | 2017-06-20 | Bayer Intelectual Property Gmbh | utilização de aril- e hetaril-carboxamidas como endoparasiticidas |
| WO2014034750A1 (ja) * | 2012-08-30 | 2014-03-06 | 国立大学法人 東京大学 | 内部寄生虫防除剤 |
| EP2730570A1 (de) | 2012-11-13 | 2014-05-14 | Bayer CropScience AG | Pyridyloxyalkylcarboxamide und deren Verwendung als Endoparasitizide und Nematizide |
| TR201816541T4 (tr) * | 2013-06-26 | 2018-11-21 | Syngenta Participations Ag | Bir pirazol-karboksamidin stereoselektif hazırlanmasına yönelik proses. |
| WO2016066580A2 (en) * | 2014-10-29 | 2016-05-06 | Bayer Cropscience Aktiengesellschaft | N-substituted phenethylcarboxamides as fungicides |
| WO2016066639A1 (en) * | 2014-10-29 | 2016-05-06 | Bayer Cropscience Aktiengesellschaft | N-(2-substituted 2-phenylethyl)carboxamides and n-(2-substituted 2-phenylethyl)-thiocarboxamides as fungicides |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2052612T3 (es) | 1987-01-30 | 1994-07-16 | Ciba Geigy Ag | Agentes microbicidas. |
| GB8714920D0 (en) | 1987-06-25 | 1987-07-29 | Shell Int Research | Thiazole derivatives |
| JPH09176125A (ja) * | 1995-05-31 | 1997-07-08 | Nissan Chem Ind Ltd | 5−ピラゾールカルボン酸アミド誘導体および植物病害防除剤 |
| JP4689042B2 (ja) * | 1998-11-04 | 2011-05-25 | 明治製菓株式会社 | ピコリン酸アミド誘導体、それを有効成分として含有する有害生物防除剤 |
| WO2001054506A1 (en) * | 2000-01-28 | 2001-08-02 | Akkadix Corporation | Methods for killing nematodes and nematode eggs using bis-amino-1,2,4-thiadiazoles |
| JP4517454B2 (ja) * | 2000-06-01 | 2010-08-04 | 宇部興産株式会社 | 4−(1−フルオロエチル)チアゾール−5−カルボン酸アミド誘導体及び農園芸用の有害生物防除剤 |
| JP4378855B2 (ja) | 2000-06-05 | 2009-12-09 | 宇部興産株式会社 | 5−(1−フルオロエチル)−1−メチルピラゾール−4−カルボン酸アミド誘導体及び農園芸用の有害生物防除剤 |
| JP4378854B2 (ja) * | 2000-06-05 | 2009-12-09 | 宇部興産株式会社 | 3−(1−フルオロエチル)−1−メチルピラゾール−4−カルボン酸アミド誘導体及び農園芸用の有害生物防除剤 |
| JP4423752B2 (ja) * | 2000-06-07 | 2010-03-03 | 宇部興産株式会社 | 5−(1−フルオロエチル)−3−メチルイソオキサゾール−4−カルボン酸誘導体及び農園芸用の有害生物防除剤 |
| US6995162B2 (en) * | 2001-01-12 | 2006-02-07 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| ATE455104T1 (de) * | 2001-11-01 | 2010-01-15 | Icagen Inc | Pyrazolamide zur anwendung in der behandlung von schmerz |
| AU2003266316B2 (en) * | 2002-08-12 | 2007-10-25 | Bayer S.A.S. | Novel 2-pyridylethylbenzamide derivative |
| EP1449841A1 (en) * | 2003-02-19 | 2004-08-25 | Bayer CropScience SA | New fungicidal compounds |
| JP2007277096A (ja) * | 2004-07-15 | 2007-10-25 | Astellas Pharma Inc | フェネチルニコチンアミド誘導体含有医薬 |
| US7786040B2 (en) | 2005-02-24 | 2010-08-31 | Nihon Nohyaku Co., Ltd. | 4-cyclopropyl-1,2,3,-thiadiazole compound, agrohorticultural plant disease controlling agent and method of using the same |
-
2005
- 2005-11-22 EP EP05356203A patent/EP1787981A1/en not_active Withdrawn
-
2006
- 2006-11-21 PT PT06830070T patent/PT1954674E/pt unknown
- 2006-11-21 EP EP06830070.6A patent/EP1954674B1/en not_active Not-in-force
- 2006-11-21 WO PCT/EP2006/068723 patent/WO2007060166A1/en not_active Ceased
- 2006-11-21 PL PL06830070.6T patent/PL1954674T3/pl unknown
- 2006-11-21 JP JP2008541734A patent/JP5363815B2/ja not_active Expired - Fee Related
- 2006-11-21 ES ES06830070.6T patent/ES2575987T3/es active Active
- 2006-11-21 US US12/085,378 patent/US9440946B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20090170924A1 (en) | 2009-07-02 |
| JP2009516722A (ja) | 2009-04-23 |
| EP1954674A1 (en) | 2008-08-13 |
| PT1954674E (pt) | 2016-06-20 |
| PL1954674T3 (pl) | 2016-09-30 |
| EP1787981A1 (en) | 2007-05-23 |
| US9440946B2 (en) | 2016-09-13 |
| WO2007060166A1 (en) | 2007-05-31 |
| EP1954674B1 (en) | 2016-03-16 |
| JP5363815B2 (ja) | 2013-12-11 |
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