TWI720023B - 作為殺害蟲劑之2-(雜)芳基-取代之稠合雜環衍生物 - Google Patents

Info

Publication number

TWI720023B

TWI720023B TW105130960A TW105130960A TWI720023B TW I720023 B TWI720023 B TW I720023B TW 105130960 A TW105130960 A TW 105130960A TW 105130960 A TW105130960 A TW 105130960A TW I720023 B TWI720023 B TW I720023B

Authority

TW

Taiwan

Prior art keywords

alkyl

spp

alkoxy

group

cycloalkyl

Prior art date

2015-09-28

Links

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• 125000000623 heterocyclic group Chemical group 0.000 title claims description 16
• 239000000575 pesticide Substances 0.000 title description 14
• 150000001875 compounds Chemical class 0.000 claims abstract description 258
• 238000000034 method Methods 0.000 claims abstract description 101
• 241001465754 Metazoa Species 0.000 claims abstract description 53
• 238000002360 preparation method Methods 0.000 claims abstract description 53
• 241000607479 Yersinia pestis Species 0.000 claims abstract description 38
• -1 cyano, carboxy Chemical group 0.000 claims description 135
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 130
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 114
• 125000001424 substituent group Chemical group 0.000 claims description 72
• 125000005843 halogen group Chemical group 0.000 claims description 62
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 43
• 239000000460 chlorine Substances 0.000 claims description 36
• 229910052801 chlorine Inorganic materials 0.000 claims description 36
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 34
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 34
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 33
• 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 claims description 33
• 239000001257 hydrogen Substances 0.000 claims description 33
• 229910052739 hydrogen Inorganic materials 0.000 claims description 33
• 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 33
• UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 33
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 32
• 125000001072 heteroaryl group Chemical group 0.000 claims description 30
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 27
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 26
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 26
• 125000003282 alkyl amino group Chemical group 0.000 claims description 26
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 26
• 229910052794 bromium Inorganic materials 0.000 claims description 26
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 25
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 24
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 24
• 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims description 23
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 21
• 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims description 21
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 21
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 20
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 20
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 19
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 19
• 125000005159 cyanoalkoxy group Chemical group 0.000 claims description 19
• 229910052757 nitrogen Inorganic materials 0.000 claims description 19
• 229920006395 saturated elastomer Polymers 0.000 claims description 18
• 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 17
• 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 17
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 17
• 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 17
• 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 16
• 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 16
• 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 16
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 16
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 16
• 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims description 16
• 239000011737 fluorine Substances 0.000 claims description 16
• 229910052731 fluorine Inorganic materials 0.000 claims description 16
• ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 16
• 125000005103 alkyl silyl group Chemical group 0.000 claims description 15
• 125000003118 aryl group Chemical class 0.000 claims description 15
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
• 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 14
• 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 14
• 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 14
• 125000000232 haloalkynyl group Chemical group 0.000 claims description 14
• 125000005842 heteroatom Chemical group 0.000 claims description 14
• 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 13
• 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims description 13
• 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims description 13
• 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims description 13
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 13
• 150000001335 aliphatic alkanes Chemical group 0.000 claims description 13
• 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 13
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 13
• 125000000262 haloalkenyl group Chemical group 0.000 claims description 13
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 13
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 13
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 13
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 13
• 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims description 12
• 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 12
• 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 12
• 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 12
• 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 12
• 125000004414 alkyl thio group Chemical group 0.000 claims description 12
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 12
• 125000004966 cyanoalkyl group Chemical group 0.000 claims description 12
• 125000004122 cyclic group Chemical group 0.000 claims description 12
• 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 12
• 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 claims description 12
• 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims description 12
• 125000004995 haloalkylthio group Chemical group 0.000 claims description 12
• 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 12
• 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 claims description 11
• 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 11
• 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 11
• 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims description 11
• 239000003905 agrochemical Substances 0.000 claims description 11
• 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 11
• 150000001412 amines Chemical class 0.000 claims description 11
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 11
• 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 10
• 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 claims description 10
• 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 10
• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 10
• 125000004758 (C1-C4) alkoxyimino group Chemical group 0.000 claims description 9
• 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 9
• 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims description 9
• 125000005089 alkenylaminocarbonyl group Chemical group 0.000 claims description 9
• 229910052799 carbon Inorganic materials 0.000 claims description 9
• 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 9
• 229910052717 sulfur Inorganic materials 0.000 claims description 9
• 239000004606 Fillers/Extenders Substances 0.000 claims description 8
• 125000002619 bicyclic group Chemical group 0.000 claims description 8
• CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 claims description 8
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
• 125000004691 alkyl thio carbonyl group Chemical group 0.000 claims description 7
• 125000004432 carbon atom Chemical group C* 0.000 claims description 7
• 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 7
• 239000007983 Tris buffer Substances 0.000 claims description 6
• LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 claims description 6
• 125000003277 amino group Chemical group 0.000 claims description 6
• 229910052760 oxygen Inorganic materials 0.000 claims description 6
• 238000006467 substitution reaction Methods 0.000 claims description 5
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
• MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 claims description 5
• 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 4
• 125000002947 alkylene group Chemical group 0.000 claims description 3
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
• 125000006001 difluoroethyl group Chemical group 0.000 claims description 3
• 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 3
• 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 3
• 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 3
• 239000004094 surface-active agent Substances 0.000 claims description 3
• 125000006337 tetrafluoro ethyl group Chemical group 0.000 claims description 3
• 150000001924 cycloalkanes Chemical group 0.000 claims description 2
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
• 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims 1
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• 239000002904 solvent Substances 0.000 description 54
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 48
• 238000006243 chemical reaction Methods 0.000 description 43
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