TW201408646A - ５－鹵基吡唑氫茚基羧醯胺類 - Google Patents

Info

Publication number

TW201408646A

TW201408646A TW102116310A TW102116310A TW201408646A TW 201408646 A TW201408646 A TW 201408646A TW 102116310 A TW102116310 A TW 102116310A TW 102116310 A TW102116310 A TW 102116310A TW 201408646 A TW201408646 A TW 201408646A

Authority

TW

Taiwan

Prior art keywords

group

alkyl

cycloalkyl

optionally substituted

different

Prior art date

2012-05-09

Links

• Espacenet
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• DZGMFITYAJIDHR-UHFFFAOYSA-N 2,3-dihydro-1h-indene-1-carboxamide Chemical class C1=CC=C2C(C(=O)N)CCC2=C1 DZGMFITYAJIDHR-UHFFFAOYSA-N 0.000 title 1
• -1 indanyl carboxamides Chemical class 0.000 claims abstract description 137
• 239000000203 mixture Substances 0.000 claims abstract description 129
• 150000001875 compounds Chemical class 0.000 claims abstract description 108
• 238000000034 method Methods 0.000 claims abstract description 77
• 230000008569 process Effects 0.000 claims abstract description 30
• 125000005843 halogen group Chemical group 0.000 claims description 89
• 108090000623 proteins and genes Proteins 0.000 claims description 85
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 82
• 229910052799 carbon Inorganic materials 0.000 claims description 70
• 239000004480 active ingredient Substances 0.000 claims description 69
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 68
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 68
• 239000000460 chlorine Substances 0.000 claims description 65
• 229910052801 chlorine Inorganic materials 0.000 claims description 65
• 239000001257 hydrogen Substances 0.000 claims description 58
• 229910052739 hydrogen Inorganic materials 0.000 claims description 58
• 239000004009 herbicide Substances 0.000 claims description 57
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 55
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 54
• 239000011737 fluorine Substances 0.000 claims description 54
• 229910052731 fluorine Inorganic materials 0.000 claims description 54
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 51
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 38
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 37
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 36
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 34
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 34
• 241000233866 Fungi Species 0.000 claims description 33
• 150000002431 hydrogen Chemical group 0.000 claims description 33
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 32
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 29
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 29
• 229910052794 bromium Inorganic materials 0.000 claims description 29
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 28
• 239000002253 acid Substances 0.000 claims description 23
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 23
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 19
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 18
• 230000003032 phytopathogenic effect Effects 0.000 claims description 18
• 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 16
• 125000000217 alkyl group Chemical group 0.000 claims description 16
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
• 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 15
• 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 15
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• 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 12
• 125000003118 aryl group Chemical group 0.000 claims description 12
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 12
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
• 125000001424 substituent group Chemical group 0.000 claims description 12
• 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 11
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 11
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• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 11
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• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 9
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• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
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• 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 6
• 125000006711 (C2-C12) alkynyl group Chemical group 0.000 claims description 6
• MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 6
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• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
• 229920006395 saturated elastomer Polymers 0.000 claims description 5
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
• 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 4
• 239000007822 coupling agent Substances 0.000 claims description 4
• 239000011593 sulfur Substances 0.000 claims description 4
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 3
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
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• 125000001769 aryl amino group Chemical group 0.000 claims description 3
• 239000003899 bactericide agent Substances 0.000 claims description 3
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
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• 125000000623 heterocyclic group Chemical group 0.000 claims description 3
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• 125000004001 thioalkyl group Chemical group 0.000 claims description 3
• 125000003396 thiol group Chemical group [H]S* 0.000 claims description 3
• 230000000895 acaricidal effect Effects 0.000 claims description 2
• 239000000642 acaricide Substances 0.000 claims description 2
• 125000003545 alkoxy group Chemical group 0.000 claims description 2
• 125000005164 aryl thioalkyl group Chemical group 0.000 claims description 2
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• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
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• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 8
• 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 claims 1
• 125000000879 imine group Chemical group 0.000 claims 1
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