MX2007014138A - Compuestos con estructura de 1-(imidazolin-2-il)amino-1,2- difenile tano para combatir plagas animales. - Google Patents

Info

Publication number

MX2007014138A

MX2007014138A MX2007014138A MX2007014138A MX2007014138A MX 2007014138 A MX2007014138 A MX 2007014138A MX 2007014138 A MX2007014138 A MX 2007014138A MX 2007014138 A MX2007014138 A MX 2007014138A MX 2007014138 A MX2007014138 A MX 2007014138A

Authority

MX

Mexico

Prior art keywords

alkyl

radicals

compounds

formula

alkylthio

Prior art date

2005-05-24

Links

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• Global Dossier
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• 241000607479 Yersinia pestis Species 0.000 title claims abstract description 64
• 241001465754 Metazoa Species 0.000 title claims abstract description 46
• FJQSHBIFQJVWAR-UHFFFAOYSA-N n-(1,2-diphenylethyl)-4,5-dihydro-1h-imidazol-2-amine Chemical class C=1C=CC=CC=1CC(C=1C=CC=CC=1)NC1=NCCN1 FJQSHBIFQJVWAR-UHFFFAOYSA-N 0.000 title abstract 2
• -1 1-(imidazolin-2-yl)amino-1 ,2- diphenylethane compound Chemical class 0.000 claims abstract description 294
• 150000001875 compounds Chemical class 0.000 claims abstract description 152
• 239000000203 mixture Substances 0.000 claims abstract description 82
• 238000000034 method Methods 0.000 claims abstract description 39
• 150000003839 salts Chemical class 0.000 claims abstract description 29
• 239000000463 material Substances 0.000 claims abstract description 20
• 206010061217 Infestation Diseases 0.000 claims abstract description 12
• 125000000217 alkyl group Chemical group 0.000 claims description 42
• 241000238631 Hexapoda Species 0.000 claims description 40
• 241000244206 Nematoda Species 0.000 claims description 32
• 125000004432 carbon atom Chemical group C* 0.000 claims description 31
• 239000001257 hydrogen Substances 0.000 claims description 30
• 229910052739 hydrogen Inorganic materials 0.000 claims description 30
• 229910052736 halogen Inorganic materials 0.000 claims description 25
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 22
• 239000002689 soil Substances 0.000 claims description 21
• 241000239223 Arachnida Species 0.000 claims description 18
• 239000000575 pesticide Substances 0.000 claims description 18
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
• 150000002367 halogens Chemical class 0.000 claims description 16
• 239000007787 solid Substances 0.000 claims description 15
• 125000003342 alkenyl group Chemical group 0.000 claims description 14
• 150000002431 hydrogen Chemical group 0.000 claims description 14
• 125000000304 alkynyl group Chemical group 0.000 claims description 13
• 230000000361 pesticidal effect Effects 0.000 claims description 13
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
• 125000003545 alkoxy group Chemical group 0.000 claims description 12
• 229910052717 sulfur Inorganic materials 0.000 claims description 12
• 235000013305 food Nutrition 0.000 claims description 11
• 241001124076 Aphididae Species 0.000 claims description 10
• 229910052799 carbon Inorganic materials 0.000 claims description 10
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
• 125000004434 sulfur atom Chemical group 0.000 claims description 9
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
• 239000007788 liquid Substances 0.000 claims description 8
• 239000004094 surface-active agent Substances 0.000 claims description 8
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 7
• 239000011593 sulfur Substances 0.000 claims description 7
• DYXWASYPBSFSKL-UHFFFAOYSA-N 1-(4,5-dihydro-1h-imidazol-2-yl)-1,2-diphenylethanamine Chemical compound N=1CCNC=1C(C=1C=CC=CC=1)(N)CC1=CC=CC=C1 DYXWASYPBSFSKL-UHFFFAOYSA-N 0.000 claims description 6
• 125000003302 alkenyloxy group Chemical group 0.000 claims description 6
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 5
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
• 125000005133 alkynyloxy group Chemical group 0.000 claims description 5
• 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims description 5
• 125000005842 heteroatom Chemical group 0.000 claims description 5
• 229910052740 iodine Inorganic materials 0.000 claims description 5
• 229920006395 saturated elastomer Polymers 0.000 claims description 5
• 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 4
• 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 4
• 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 4
• 229910003827 NRaRb Inorganic materials 0.000 claims description 4
• 230000009418 agronomic effect Effects 0.000 claims description 4
• 125000001188 haloalkyl group Chemical group 0.000 claims description 4
• 125000005843 halogen group Chemical group 0.000 claims description 4
• 125000000623 heterocyclic group Chemical group 0.000 claims description 4
• 125000002950 monocyclic group Chemical group 0.000 claims description 4
• 229910052757 nitrogen Inorganic materials 0.000 claims description 4
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
• 238000009331 sowing Methods 0.000 claims description 4
• 125000005109 alkynylthio group Chemical group 0.000 claims description 3
• 125000004429 atom Chemical group 0.000 claims description 3
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
• 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 3
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
• 229910052760 oxygen Inorganic materials 0.000 claims description 3
• 239000001301 oxygen Substances 0.000 claims description 3
• 125000006799 (C2-C6) alkenylamino group Chemical group 0.000 claims description 2
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
• 125000005137 alkenylsulfonyl group Chemical group 0.000 claims description 2
• 125000005139 alkynylsulfonyl group Chemical group 0.000 claims description 2
• 238000009395 breeding Methods 0.000 claims description 2
• 230000001488 breeding effect Effects 0.000 claims description 2
• 230000035784 germination Effects 0.000 claims description 2
• 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 description 2
• 125000001624 naphthyl group Chemical group 0.000 claims description 2
• 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 4
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
• ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
• 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 2
• 125000006728 (C1-C6) alkynyl group Chemical group 0.000 claims 1
• 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 1
• DTGGNTMERRTPLR-UHFFFAOYSA-N 1,2-diphenylethanamine Chemical compound C=1C=CC=CC=1C(N)CC1=CC=CC=C1 DTGGNTMERRTPLR-UHFFFAOYSA-N 0.000 claims 1
• 229910006069 SO3H Inorganic materials 0.000 claims 1
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
• 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
• 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 1
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
• MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 1
• 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
• 230000001747 exhibiting effect Effects 0.000 claims 1
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
• 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
• 241000196324 Embryophyta Species 0.000 description 39
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
• 150000003254 radicals Chemical class 0.000 description 25
• 238000009472 formulation Methods 0.000 description 22
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• 239000003921 oil Substances 0.000 description 19
• 241000255925 Diptera Species 0.000 description 18
• 239000008187 granular material Substances 0.000 description 18
• 239000000843 powder Substances 0.000 description 18
• 241000894007 species Species 0.000 description 13
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
• 239000000243 solution Substances 0.000 description 12
• 239000003795 chemical substances by application Substances 0.000 description 11
• 239000006185 dispersion Substances 0.000 description 11
• 239000000047 product Substances 0.000 description 11
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
• 239000000839 emulsion Substances 0.000 description 10
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
• 241000257303 Hymenoptera Species 0.000 description 9
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
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