TW201036966A - Fungicidal heterocyclic compounds - Google Patents
Fungicidal heterocyclic compounds Download PDFInfo
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- TW201036966A TW201036966A TW098141182A TW98141182A TW201036966A TW 201036966 A TW201036966 A TW 201036966A TW 098141182 A TW098141182 A TW 098141182A TW 98141182 A TW98141182 A TW 98141182A TW 201036966 A TW201036966 A TW 201036966A
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- 230000000855 fungicidal effect Effects 0.000 title claims 111
- 150000002391 heterocyclic compounds Chemical class 0.000 title claims 6
- 150000001875 compounds Chemical class 0.000 claims abstract 433
- 239000000203 mixture Substances 0.000 claims abstract 131
- 238000000034 method Methods 0.000 claims abstract 59
- 150000003839 salts Chemical class 0.000 claims abstract 43
- 201000010099 disease Diseases 0.000 claims abstract 24
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract 24
- 244000053095 fungal pathogen Species 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims 252
- -1 c2-c6-alkenyl group Chemical group 0.000 claims 237
- 239000000417 fungicide Substances 0.000 claims 179
- 125000003545 alkoxy group Chemical group 0.000 claims 176
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine group Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 157
- 125000001424 substituent group Chemical group 0.000 claims 122
- 101100258328 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) crc-2 gene Proteins 0.000 claims 96
- 125000004429 atom Chemical group 0.000 claims 94
- 125000004093 cyano group Chemical group *C#N 0.000 claims 92
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 79
- 125000005842 heteroatom Chemical group 0.000 claims 67
- 229910052799 carbon Inorganic materials 0.000 claims 66
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 63
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 63
- 229910052736 halogen Inorganic materials 0.000 claims 61
- 150000001721 carbon Chemical group 0.000 claims 59
- 150000002367 halogens Chemical class 0.000 claims 53
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 52
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims 52
- 125000004432 carbon atom Chemical group C* 0.000 claims 50
- 241000196324 Embryophyta Species 0.000 claims 49
- 238000002360 preparation method Methods 0.000 claims 47
- 125000001188 haloalkyl group Chemical group 0.000 claims 46
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 45
- 150000001412 amines Chemical class 0.000 claims 44
- 125000005843 halogen group Chemical group 0.000 claims 42
- COLOHWPRNRVWPI-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical group [CH2]C(F)(F)F COLOHWPRNRVWPI-UHFFFAOYSA-N 0.000 claims 41
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 38
- 125000004122 cyclic group Chemical group 0.000 claims 37
- 125000004438 haloalkoxy group Chemical group 0.000 claims 37
- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 35
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 33
- 239000002253 acid Substances 0.000 claims 33
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 33
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 31
- 239000011541 reaction mixture Substances 0.000 claims 31
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 30
- 241000233866 Fungi Species 0.000 claims 29
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 29
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 29
- 229910052757 nitrogen Inorganic materials 0.000 claims 29
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 28
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims 28
- 235000019439 ethyl acetate Nutrition 0.000 claims 28
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 27
- 125000003342 alkenyl group Chemical group 0.000 claims 27
- 125000000623 heterocyclic group Chemical group 0.000 claims 27
- 239000000243 solution Substances 0.000 claims 27
- 230000015572 biosynthetic process Effects 0.000 claims 26
- 239000007787 solid Substances 0.000 claims 26
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 25
- 150000002923 oximes Chemical group 0.000 claims 25
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 24
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 24
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 23
- 238000009472 formulation Methods 0.000 claims 23
- 239000007788 liquid Substances 0.000 claims 23
- 239000000460 chlorine Substances 0.000 claims 22
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims 22
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 22
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 22
- 125000004414 alkyl thio group Chemical group 0.000 claims 21
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims 21
- 238000006243 chemical reaction Methods 0.000 claims 21
- 239000003112 inhibitor Substances 0.000 claims 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 21
- 239000000047 product Substances 0.000 claims 21
- 239000002904 solvent Substances 0.000 claims 21
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 claims 20
- 206010036790 Productive cough Diseases 0.000 claims 20
- 125000003282 alkyl amino group Chemical group 0.000 claims 20
- 125000000304 alkynyl group Chemical group 0.000 claims 20
- 229940126214 compound 3 Drugs 0.000 claims 20
- 210000003802 sputum Anatomy 0.000 claims 20
- 208000024794 sputum Diseases 0.000 claims 20
- ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 claims 19
- ITOFPJRDSCGOSA-KZLRUDJFSA-N (2s)-2-[[(4r)-4-[(3r,5r,8r,9s,10s,13r,14s,17r)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H](CC[C@]13C)[C@@H]2[C@@H]3CC[C@@H]1[C@H](C)CCC(=O)N[C@H](C(O)=O)CC1=CNC2=CC=CC=C12 ITOFPJRDSCGOSA-KZLRUDJFSA-N 0.000 claims 19
- 125000003118 aryl group Chemical group 0.000 claims 19
- 229940126142 compound 16 Drugs 0.000 claims 19
- 229940125782 compound 2 Drugs 0.000 claims 19
- 229940125810 compound 20 Drugs 0.000 claims 19
- 230000012010 growth Effects 0.000 claims 19
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 18
- PYRKKGOKRMZEIT-UHFFFAOYSA-N 2-[6-(2-cyclopropylethoxy)-9-(2-hydroxy-2-methylpropyl)-1h-phenanthro[9,10-d]imidazol-2-yl]-5-fluorobenzene-1,3-dicarbonitrile Chemical compound C1=C2C3=CC(CC(C)(O)C)=CC=C3C=3NC(C=4C(=CC(F)=CC=4C#N)C#N)=NC=3C2=CC=C1OCCC1CC1 PYRKKGOKRMZEIT-UHFFFAOYSA-N 0.000 claims 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 18
- LJOOWESTVASNOG-UFJKPHDISA-N [(1s,3r,4ar,7s,8s,8as)-3-hydroxy-8-[2-[(4r)-4-hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl] (2s)-2-methylbutanoate Chemical compound C([C@H]1[C@@H](C)C=C[C@H]2C[C@@H](O)C[C@@H]([C@H]12)OC(=O)[C@@H](C)CC)CC1C[C@@H](O)CC(=O)O1 LJOOWESTVASNOG-UFJKPHDISA-N 0.000 claims 18
- 239000003795 chemical substances by application Substances 0.000 claims 18
- 229940127204 compound 29 Drugs 0.000 claims 18
- 125000004663 dialkyl amino group Chemical group 0.000 claims 18
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 18
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 18
- DYGBNAYFDZEYBA-UHFFFAOYSA-N n-(cyclopropylmethyl)-2-[4-(4-methoxybenzoyl)piperidin-1-yl]-n-[(4-oxo-1,5,7,8-tetrahydropyrano[4,3-d]pyrimidin-2-yl)methyl]acetamide Chemical compound C1=CC(OC)=CC=C1C(=O)C1CCN(CC(=O)N(CC2CC2)CC=2NC(=O)C=3COCCC=3N=2)CC1 DYGBNAYFDZEYBA-UHFFFAOYSA-N 0.000 claims 18
- 125000001624 naphthyl group Chemical group 0.000 claims 18
- 229920006395 saturated elastomer Polymers 0.000 claims 18
- 125000004434 sulfur atom Chemical group 0.000 claims 18
- UDQTXCHQKHIQMH-KYGLGHNPSA-N (3ar,5s,6s,7r,7ar)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3ah-pyrano[3,2-d][1,3]thiazole-6,7-diol Chemical compound S1C(NCC)=N[C@H]2[C@@H]1O[C@H](C(F)F)[C@@H](O)[C@@H]2O UDQTXCHQKHIQMH-KYGLGHNPSA-N 0.000 claims 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 17
- 229940125936 compound 42 Drugs 0.000 claims 17
- 239000003085 diluting agent Substances 0.000 claims 17
- 229910052739 hydrogen Inorganic materials 0.000 claims 17
- 230000002829 reductive effect Effects 0.000 claims 17
- 239000000126 substance Substances 0.000 claims 17
- 229910052717 sulfur Inorganic materials 0.000 claims 17
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 claims 16
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims 16
- 229940125904 compound 1 Drugs 0.000 claims 16
- 125000000232 haloalkynyl group Chemical group 0.000 claims 16
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 16
- 239000004094 surface-active agent Substances 0.000 claims 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 15
- 230000009471 action Effects 0.000 claims 15
- 239000004480 active ingredient Substances 0.000 claims 15
- 229910052794 bromium Inorganic materials 0.000 claims 15
- 230000002538 fungal effect Effects 0.000 claims 15
- 239000007789 gas Substances 0.000 claims 15
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- 235000019198 oils Nutrition 0.000 claims 15
- 239000005864 Sulphur Substances 0.000 claims 14
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 14
- 238000006467 substitution reaction Methods 0.000 claims 14
- 150000003573 thiols Chemical class 0.000 claims 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 13
- 230000005764 inhibitory process Effects 0.000 claims 13
- 150000002576 ketones Chemical class 0.000 claims 13
- 238000003786 synthesis reaction Methods 0.000 claims 13
- 241000894006 Bacteria Species 0.000 claims 12
- 125000003302 alkenyloxy group Chemical group 0.000 claims 12
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 12
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 12
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 12
- 230000008569 process Effects 0.000 claims 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 12
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 11
- AIKKULXCBHRFOS-UHFFFAOYSA-N Formothion Chemical compound COP(=S)(OC)SCC(=O)N(C)C=O AIKKULXCBHRFOS-UHFFFAOYSA-N 0.000 claims 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 11
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 11
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 11
- 150000001336 alkenes Chemical class 0.000 claims 11
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 11
- 239000003153 chemical reaction reagent Substances 0.000 claims 11
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- 239000012044 organic layer Substances 0.000 claims 11
- 229910052760 oxygen Inorganic materials 0.000 claims 11
- 244000052769 pathogen Species 0.000 claims 11
- 239000004575 stone Substances 0.000 claims 11
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 11
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical class NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 claims 10
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims 10
- 101150041968 CDC13 gene Proteins 0.000 claims 10
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims 10
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 10
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 claims 10
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 10
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 10
- 125000005133 alkynyloxy group Chemical group 0.000 claims 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 10
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- 239000001301 oxygen Substances 0.000 claims 10
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- QSLPNSWXUQHVLP-UHFFFAOYSA-N $l^{1}-sulfanylmethane Chemical compound [S]C QSLPNSWXUQHVLP-UHFFFAOYSA-N 0.000 claims 9
- 241000237858 Gastropoda Species 0.000 claims 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims 9
- 125000006242 amine protecting group Chemical group 0.000 claims 9
- 125000003277 amino group Chemical group 0.000 claims 9
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 9
- 125000000262 haloalkenyl group Chemical group 0.000 claims 9
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 9
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 9
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 9
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- VYBULKYOUJBBPW-UHFFFAOYSA-N 1-amino-3-iminothiourea Chemical compound NNC(=S)N=N VYBULKYOUJBBPW-UHFFFAOYSA-N 0.000 claims 8
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 8
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- 125000002837 carbocyclic group Chemical group 0.000 claims 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims 8
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 8
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- 125000000524 functional group Chemical group 0.000 claims 8
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- 125000001072 heteroaryl group Chemical group 0.000 claims 8
- 125000000842 isoxazolyl group Chemical group 0.000 claims 8
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- 239000002689 soil Substances 0.000 claims 8
- 238000012360 testing method Methods 0.000 claims 8
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- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 7
- 125000005577 anthracene group Chemical group 0.000 claims 7
- 125000002619 bicyclic group Chemical group 0.000 claims 7
- 239000003139 biocide Substances 0.000 claims 7
- 210000004027 cell Anatomy 0.000 claims 7
- 238000010168 coupling process Methods 0.000 claims 7
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- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims 7
- 238000011161 development Methods 0.000 claims 7
- 230000018109 developmental process Effects 0.000 claims 7
- 230000000694 effects Effects 0.000 claims 7
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 7
- 125000004995 haloalkylthio group Chemical group 0.000 claims 7
- 229910052740 iodine Inorganic materials 0.000 claims 7
- 230000002147 killing effect Effects 0.000 claims 7
- 229910052707 ruthenium Inorganic materials 0.000 claims 7
- 229910021653 sulphate ion Inorganic materials 0.000 claims 7
- 239000005730 Azoxystrobin Substances 0.000 claims 6
- 239000005944 Chlorpyrifos Substances 0.000 claims 6
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- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims 1
- 238000007790 scraping Methods 0.000 claims 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims 1
- 150000003335 secondary amines Chemical class 0.000 claims 1
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- 235000015170 shellfish Nutrition 0.000 claims 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 claims 1
- 229910021647 smectite Inorganic materials 0.000 claims 1
- 229910000029 sodium carbonate Inorganic materials 0.000 claims 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 claims 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims 1
- 229960001922 sodium perborate Drugs 0.000 claims 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 claims 1
- 108010025009 spectrin-like proteins Proteins 0.000 claims 1
- 238000001228 spectrum Methods 0.000 claims 1
- 238000013125 spirometry Methods 0.000 claims 1
- 210000003046 sporozoite Anatomy 0.000 claims 1
- 238000001694 spray drying Methods 0.000 claims 1
- 238000010561 standard procedure Methods 0.000 claims 1
- 230000001954 sterilising effect Effects 0.000 claims 1
- 238000004659 sterilization and disinfection Methods 0.000 claims 1
- 239000000021 stimulant Substances 0.000 claims 1
- 229960005322 streptomycin Drugs 0.000 claims 1
- 229910052712 strontium Inorganic materials 0.000 claims 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 150000003890 succinate salts Chemical class 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- 150000008163 sugars Chemical class 0.000 claims 1
- 150000004763 sulfides Chemical class 0.000 claims 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
- 150000003871 sulfonates Chemical class 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 229960005559 sulforaphane Drugs 0.000 claims 1
- 235000015487 sulforaphane Nutrition 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
- 150000003463 sulfur Chemical class 0.000 claims 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims 1
- 239000001117 sulphuric acid Substances 0.000 claims 1
- 235000011149 sulphuric acid Nutrition 0.000 claims 1
- 239000013589 supplement Substances 0.000 claims 1
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- 239000004546 suspension concentrate Substances 0.000 claims 1
- 239000004548 suspo-emulsion Substances 0.000 claims 1
- 230000009885 systemic effect Effects 0.000 claims 1
- 239000003760 tallow Substances 0.000 claims 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 claims 1
- 229960002722 terbinafine Drugs 0.000 claims 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 claims 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 claims 1
- POOSGDOYLQNASK-UHFFFAOYSA-N tetracosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC POOSGDOYLQNASK-UHFFFAOYSA-N 0.000 claims 1
- 125000000383 tetramethylene group Chemical class [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 claims 1
- 150000003535 tetraterpenes Chemical class 0.000 claims 1
- 235000009657 tetraterpenes Nutrition 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- 125000004001 thioalkyl group Chemical group 0.000 claims 1
- 229940071127 thioglycolate Drugs 0.000 claims 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 claims 1
- 229960000790 thymol Drugs 0.000 claims 1
- 238000003971 tillage Methods 0.000 claims 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims 1
- 239000004408 titanium dioxide Substances 0.000 claims 1
- 231100000331 toxic Toxicity 0.000 claims 1
- 230000002588 toxic effect Effects 0.000 claims 1
- 108700012359 toxins Proteins 0.000 claims 1
- 238000012549 training Methods 0.000 claims 1
- 230000026683 transduction Effects 0.000 claims 1
- 238000010361 transduction Methods 0.000 claims 1
- 229960002622 triacetin Drugs 0.000 claims 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 claims 1
- 230000004102 tricarboxylic acid cycle Effects 0.000 claims 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 claims 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims 1
- GTSMGKYOGFOSAR-UHFFFAOYSA-N tridecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCCS(O)(=O)=O GTSMGKYOGFOSAR-UHFFFAOYSA-N 0.000 claims 1
- 229940087291 tridecyl alcohol Drugs 0.000 claims 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- RYYVLZVUVIJVGH-UHFFFAOYSA-N trimethylxanthine Natural products CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 claims 1
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- JOPDZQBPOWAEHC-UHFFFAOYSA-H tristrontium;diphosphate Chemical compound [Sr+2].[Sr+2].[Sr+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O JOPDZQBPOWAEHC-UHFFFAOYSA-H 0.000 claims 1
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- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims 1
- 239000010937 tungsten Substances 0.000 claims 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11913708P | 2008-12-02 | 2008-12-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201036966A true TW201036966A (en) | 2010-10-16 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW098141182A TW201036966A (en) | 2008-12-02 | 2009-12-02 | Fungicidal heterocyclic compounds |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8618137B2 (enExample) |
| EP (1) | EP2358709B1 (enExample) |
| JP (1) | JP5592894B2 (enExample) |
| KR (1) | KR101716514B1 (enExample) |
| CN (1) | CN102227423B (enExample) |
| AR (1) | AR074411A1 (enExample) |
| AU (1) | AU2009322486A1 (enExample) |
| BR (1) | BRPI0914405B8 (enExample) |
| CL (1) | CL2011001272A1 (enExample) |
| ES (1) | ES2452299T3 (enExample) |
| IL (1) | IL212186A0 (enExample) |
| MX (1) | MX2011005598A (enExample) |
| PL (1) | PL2358709T3 (enExample) |
| TW (1) | TW201036966A (enExample) |
| UY (1) | UY32285A (enExample) |
| WO (1) | WO2010065579A2 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| MX2012007200A (es) | 2009-12-21 | 2012-07-10 | Bayer Cropscience Ag | Bis(difluorometil)pirazoles como fungicidas. |
| WO2011134969A1 (de) | 2010-04-28 | 2011-11-03 | Bayer Cropscience Ag | Ketoheteroarylpiperidin und -piperazin derivate als fungizide |
| JP2013528169A (ja) | 2010-05-27 | 2013-07-08 | バイエル・クロップサイエンス・アーゲー | 殺菌剤としてのピリジニルカルボン酸誘導体 |
| US20120122928A1 (en) | 2010-08-11 | 2012-05-17 | Bayer Cropscience Ag | Heteroarylpiperidine and -Piperazine Derivatives as Fungicides |
| EP2423210A1 (de) | 2010-08-25 | 2012-02-29 | Bayer CropScience AG | Heteroarylpiperidin- und -piperazinderivate als Fungizide |
| US8759527B2 (en) | 2010-08-25 | 2014-06-24 | Bayer Cropscience Ag | Heteroarylpiperidine and -piperazine derivatives as fungicides |
| CA2815716C (en) * | 2010-10-27 | 2019-06-11 | Bayer Intellectual Property Gmbh | Heteroaryl piperidine and heteroaryl piperazine derivatives as fungicides |
| MX2013006936A (es) * | 2010-12-17 | 2013-07-22 | Du Pont | Ambas azociclicas fungicidas. |
| KR101848116B1 (ko) * | 2011-02-01 | 2018-04-11 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 살진균제로서의 헤테로아릴 피페리딘 및 헤테로아릴 피페라진 유도체 |
| JP5959646B2 (ja) | 2011-09-15 | 2016-08-02 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 殺菌剤としてのピペリジンピラゾール類 |
| BR112014016101B1 (pt) * | 2011-12-27 | 2020-03-10 | Bayer Intellectual Property Gmbh | Compostos derivados da heteroarilpiperidina e heteroarilpiperazina, método e composição para controlar microorganismos indesejados, suas utilizações e semente tratada |
| EP2809668B1 (en) | 2012-02-02 | 2017-04-12 | Actelion Pharmaceuticals Ltd. | 4-(benzoimidazol-2-yl)-thiazole compounds and related aza derivatives |
| BR122019010638B1 (pt) | 2012-02-27 | 2020-12-29 | Bayer Intellectual Property Gmbh | combinação, método para controle de fungos fitopatogênicos prejudiciais e uso da referida combinação |
| KR20150022876A (ko) * | 2012-06-22 | 2015-03-04 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 살진균제 복소환 화합물 |
| WO2014033164A1 (en) | 2012-08-30 | 2014-03-06 | Bayer Cropscience Ag | Procedure for the decarboxylation of 3,5-bis(haloalkyl)-pyrazole-4-carboxylic acid derivatives |
| EP2801575A1 (en) | 2013-05-07 | 2014-11-12 | Bayer CropScience AG | Heteroaryldihydropyridine derivatives as fungicides |
| WO2014206896A1 (en) | 2013-06-24 | 2014-12-31 | Bayer Cropscience Ag | Piperidinecarboxylic acid derivatives as fungicides |
| CN105658649B (zh) | 2013-07-22 | 2019-03-22 | 爱杜西亚药品有限公司 | 1-(哌嗪-1-基)-2-([1,2,4]三唑-1-基)-乙酮衍生物 |
| TWI646095B (zh) | 2013-08-28 | 2019-01-01 | 拜耳作物科學股份有限公司 | 作為殺真菌劑之雜芳基哌啶及－哌的丙二酸酯衍生物 |
| AR099789A1 (es) | 2014-03-24 | 2016-08-17 | Actelion Pharmaceuticals Ltd | Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina |
| BR112016021869A2 (pt) | 2014-03-24 | 2017-10-24 | Bayer Cropscience Ag | derivados de fenilpiperidinacarboxamida como fungicidas |
| MX382659B (es) * | 2014-05-28 | 2025-03-11 | Bayer Cropscience Ag | Proceso para la preparación de derivados de tiazol. |
| EP3181552B1 (en) * | 2014-08-13 | 2020-10-21 | Nippon Soda Co., Ltd. | Diaryl imidazole compound and pest control agent |
| WO2016024350A1 (ja) | 2014-08-13 | 2016-02-18 | 株式会社エス・ディー・エス バイオテック | 縮合１１員環化合物及びそれらを含有する農園芸用殺菌剤 |
| AR103399A1 (es) | 2015-01-15 | 2017-05-10 | Actelion Pharmaceuticals Ltd | Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3 |
| PE20171100A1 (es) | 2015-01-15 | 2017-08-07 | Idorsia Pharmaceuticals Ltd | Derivados de hidroxialquil-piperazina como moduladores del receptor cxcr3 |
| WO2016202761A1 (en) | 2015-06-17 | 2016-12-22 | Bayer Cropscience Aktiengesellschaft | Active compound combinations |
| CN110015977B (zh) * | 2015-12-25 | 2020-09-15 | 沈阳中化农药化工研发有限公司 | 一种丙二腈肟醚类化合物及其用途 |
| CN108601353B (zh) | 2016-02-08 | 2024-04-05 | 高文作物保护公司 | 杀菌性组合物 |
| EP3415496B1 (en) | 2016-02-08 | 2021-07-21 | Gowan Company, L.L.C. | Process for preparing 1,2-benzenedimethanol compound |
| TW201838974A (zh) | 2017-04-19 | 2018-11-01 | 印度商Ｐｉ工業公司 | 具殺菌性質之雜環化合物 |
| WO2019048988A1 (en) | 2017-09-08 | 2019-03-14 | Pi Industries Ltd. | Novel fungidal heterocyclic compounds |
| MX2020002449A (es) * | 2017-09-08 | 2020-11-06 | Pi Industries Ltd | Nuevos compuestos heterociclicos fungicidas. |
| CN111196805A (zh) * | 2018-11-17 | 2020-05-26 | 曲阜德禄生物科技有限公司 | 哌啶基噻唑甲酰胺类化合物合成方法与用途 |
| CN109516962A (zh) * | 2018-12-13 | 2019-03-26 | 天津雅奥泰克科技有限公司 | 一种合成2,6-二氟苯基-1-(4,5-二氢异恶唑)-3-乙基酮的新方法 |
| CN112189663B (zh) * | 2019-07-08 | 2022-03-22 | 沈阳中化农药化工研发有限公司 | 一种杀真菌、细菌组合物和应用 |
| CN112189661B (zh) * | 2019-07-08 | 2022-03-29 | 沈阳中化农药化工研发有限公司 | 杀真菌、细菌组合物及应用 |
| CN112189665B (zh) * | 2019-07-08 | 2022-03-22 | 沈阳中化农药化工研发有限公司 | 一种杀真菌细菌组合物和应用 |
| CN111662280B (zh) * | 2020-07-17 | 2023-03-03 | 南开大学 | 一种哌啶基四氢苯并噻唑肟醚类衍生物及应用 |
| CN112812035B (zh) * | 2021-02-01 | 2022-07-12 | 闽江学院 | 一种氟代乙醛-氧-芳基肟类化合物及其合成方法 |
| CN116199683A (zh) * | 2021-11-30 | 2023-06-02 | 江苏中旗科技股份有限公司 | 一种含有噁二唑结构的化合物及其制备方法和应用以及一种杀菌剂 |
| EP4578854A4 (en) * | 2022-08-26 | 2025-12-03 | Jiangsu Flag Chem Ind Co Ltd | COMPOUND CONTAINING A CHAIN-FORMED CARBOXYLIC ACID AMIDE STRUCTURE, ITS PREPARATION PROCESS, ITS USE AND BACTERICIDAL ACTION |
| EP4509511A1 (en) | 2023-08-17 | 2025-02-19 | Bayer Aktiengesellschaft | Substituted spiro-isoxazolinyl lactams, salts thereof and their use as herbicidally active substances |
| WO2025098238A1 (zh) * | 2023-11-07 | 2025-05-15 | 江苏中旗科技股份有限公司 | 含哌嗪环结构的化合物及其制备方法和应用、一种杀菌剂 |
| CN118878474B (zh) * | 2024-07-01 | 2025-10-28 | 盐城工学院 | 一种合成2,6-二氟苯基-1-(4,5-二氢异恶唑)-3-乙基酮的方法 |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2891855A (en) | 1954-08-16 | 1959-06-23 | Geigy Ag J R | Compositions and methods for influencing the growth of plants |
| US3235361A (en) | 1962-10-29 | 1966-02-15 | Du Pont | Method for the control of undesirable vegetation |
| US3060084A (en) | 1961-06-09 | 1962-10-23 | Du Pont | Improved homogeneous, readily dispersed, pesticidal concentrate |
| US3299566A (en) | 1964-06-01 | 1967-01-24 | Olin Mathieson | Water soluble film containing agricultural chemicals |
| US3309192A (en) | 1964-12-02 | 1967-03-14 | Du Pont | Method of controlling seedling weed grasses |
| US4144050A (en) | 1969-02-05 | 1979-03-13 | Hoechst Aktiengesellschaft | Micro granules for pesticides and process for their manufacture |
| US3920442A (en) | 1972-09-18 | 1975-11-18 | Du Pont | Water-dispersible pesticide aggregates |
| US4172714A (en) | 1976-12-20 | 1979-10-30 | E. I. Du Pont De Nemours And Company | Dry compactible, swellable herbicidal compositions and pellets produced therefrom |
| GB2095558B (en) | 1981-03-30 | 1984-10-24 | Avon Packers Ltd | Formulation of agricultural chemicals |
| DE3246493A1 (de) | 1982-12-16 | 1984-06-20 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von wasserdispergierbaren granulaten |
| US4584014A (en) | 1984-07-02 | 1986-04-22 | Rohm And Haas Company | Ethylideneaminooxyacetic acids and esters |
| DE3537762A1 (de) | 1984-12-20 | 1986-07-03 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von pyridin-carbonsaeure-n-tert.-alkylamiden |
| US5180587A (en) | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
| ES2166919T3 (es) | 1989-08-30 | 2002-05-01 | Kynoch Agrochemicals Proprieta | Preparacion de un dispositivo dosificador. |
| JPH05504964A (ja) | 1990-03-12 | 1993-07-29 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 熱―活性化結合剤からの水分散性又は水溶性有害生物防除剤顆粒 |
| EP0480679B1 (en) | 1990-10-11 | 1996-09-18 | Sumitomo Chemical Company Limited | Pesticidal composition |
| PL174704B1 (pl) | 1993-05-12 | 1998-09-30 | Du Pont | Nowe 4(3H)-chinazolinony i środek grzybobójczy do zwalczania mączniaka pszenicy |
| GB9416364D0 (en) | 1994-08-12 | 1994-10-05 | Fine Organics Ltd | Preparation of thioamides |
| ES2167586T3 (es) | 1995-07-05 | 2002-05-16 | Du Pont | Pirimidinonas fungicidas. |
| AU716248B2 (en) | 1996-03-11 | 2000-02-24 | Novartis Ag | Pyrimidin-4-one derivatives as pesticide |
| GB9719411D0 (en) | 1997-09-12 | 1997-11-12 | Ciba Geigy Ag | New Pesticides |
| AU1596101A (en) * | 1999-11-12 | 2001-06-06 | Merck & Co., Inc. | Aliphatic amine substituted piperidyl diaryl pyrrole derivatives as antiprotozoal agents |
| DE10136065A1 (de) | 2001-07-25 | 2003-02-13 | Bayer Cropscience Ag | Pyrazolylcarboxanilide |
| TW200724033A (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| TW200306155A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
| GB0230162D0 (en) | 2002-12-24 | 2003-02-05 | Metris Therapeutics Ltd | Compounds useful in inhibiting angiogenesis |
| FR2856685B1 (fr) | 2003-06-25 | 2005-09-23 | Merck Sante Sas | Derives de thiazolylpiperidine, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent |
| US20080004263A1 (en) | 2004-03-04 | 2008-01-03 | Santora Vincent J | Ligands of Follicle Stimulating Hormone Receptor and Methods of Use Thereof |
| US7713998B2 (en) | 2004-11-10 | 2010-05-11 | Ono Pharmaceutical Co., Ltd. | Nitrogenous heterocyclic compound and pharmaceutical use thereof |
| TW200738701A (en) * | 2005-07-26 | 2007-10-16 | Du Pont | Fungicidal carboxamides |
| EP1962605A2 (en) * | 2005-12-12 | 2008-09-03 | Merck & Co., Inc. | 2-arylthiazole derivatives as cxcr3 receptor modulators |
| WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
| WO2008069313A1 (ja) * | 2006-12-07 | 2008-06-12 | Japan Tobacco Inc. | ピロリジン化合物の製造方法 |
| WO2008091594A2 (en) | 2007-01-24 | 2008-07-31 | E. I. Du Pont De Nemours And Company | Fungicidal mixtures |
| JP5337711B2 (ja) | 2007-01-25 | 2013-11-06 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 殺菌性アミド |
| TWI428091B (zh) | 2007-10-23 | 2014-03-01 | Du Pont | 殺真菌劑混合物 |
| MX2010004491A (es) * | 2007-10-25 | 2010-06-21 | Astrazeneca Ab | Derivados de piridina y pirazina utiles en el tratamiento de trastornos proliferativos celulares. |
| JP5535941B2 (ja) | 2008-01-25 | 2014-07-02 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 殺菌性アミド |
| CN101970432B (zh) | 2008-01-25 | 2014-05-28 | 杜邦公司 | 杀真菌杂环化合物 |
| WO2010037479A1 (de) | 2008-10-01 | 2010-04-08 | Bayer Cropscience Ag | Heterocyclyl substituierte thiazole als pflanzenschutzmittel |
| MX2013006936A (es) * | 2010-12-17 | 2013-07-22 | Du Pont | Ambas azociclicas fungicidas. |
-
2009
- 2009-12-02 BR BRPI0914405A patent/BRPI0914405B8/pt not_active IP Right Cessation
- 2009-12-02 KR KR1020117015240A patent/KR101716514B1/ko not_active Expired - Fee Related
- 2009-12-02 TW TW098141182A patent/TW201036966A/zh unknown
- 2009-12-02 US US13/127,809 patent/US8618137B2/en active Active
- 2009-12-02 JP JP2011539643A patent/JP5592894B2/ja active Active
- 2009-12-02 EP EP09764158.3A patent/EP2358709B1/en active Active
- 2009-12-02 MX MX2011005598A patent/MX2011005598A/es active IP Right Grant
- 2009-12-02 WO PCT/US2009/066318 patent/WO2010065579A2/en not_active Ceased
- 2009-12-02 CN CN200980148160.8A patent/CN102227423B/zh not_active Expired - Fee Related
- 2009-12-02 AR ARP090104654A patent/AR074411A1/es active IP Right Grant
- 2009-12-02 ES ES09764158.3T patent/ES2452299T3/es active Active
- 2009-12-02 UY UY0001032285A patent/UY32285A/es not_active Application Discontinuation
- 2009-12-02 AU AU2009322486A patent/AU2009322486A1/en not_active Abandoned
- 2009-12-02 PL PL09764158T patent/PL2358709T3/pl unknown
-
2011
- 2011-04-06 IL IL212186A patent/IL212186A0/en unknown
- 2011-05-31 CL CL2011001272A patent/CL2011001272A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0914405B8 (pt) | 2022-12-06 |
| PL2358709T3 (pl) | 2014-06-30 |
| AU2009322486A1 (en) | 2010-06-10 |
| ES2452299T3 (es) | 2014-03-31 |
| US20110224258A1 (en) | 2011-09-15 |
| EP2358709B1 (en) | 2014-01-22 |
| UY32285A (es) | 2010-06-30 |
| AR074411A1 (es) | 2011-01-12 |
| CL2011001272A1 (es) | 2011-10-07 |
| US8618137B2 (en) | 2013-12-31 |
| WO2010065579A3 (en) | 2010-07-29 |
| BRPI0914405A2 (pt) | 2015-08-11 |
| BRPI0914405B1 (pt) | 2017-04-04 |
| WO2010065579A2 (en) | 2010-06-10 |
| IL212186A0 (en) | 2011-06-30 |
| CN102227423A (zh) | 2011-10-26 |
| CN102227423B (zh) | 2015-06-17 |
| EP2358709A2 (en) | 2011-08-24 |
| KR20110091798A (ko) | 2011-08-12 |
| KR101716514B1 (ko) | 2017-03-14 |
| MX2011005598A (es) | 2011-06-16 |
| JP2012510520A (ja) | 2012-05-10 |
| JP5592894B2 (ja) | 2014-09-17 |
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