UA81281C2 - Avermectin derivatives, pesticide composition and method of pest control - Google Patents

Info

Publication number

UA81281C2

UA81281C2 UAA200507209A UA2005007209A UA81281C2 UA 81281 C2 UA81281 C2 UA 81281C2 UA A200507209 A UAA200507209 A UA A200507209A UA 2005007209 A UA2005007209 A UA 2005007209A UA 81281 C2 UA81281 C2 UA 81281C2

Authority

UA

Ukraine

Prior art keywords

alkyl

heterocyclyl

aryl

formula

group

Prior art date

2002-12-20

Links

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• Global Dossier
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• 239000000203 mixture Substances 0.000 title claims abstract description 91
• 239000000575 pesticide Substances 0.000 title claims abstract description 5
• 238000000034 method Methods 0.000 title claims description 34
• 241000607479 Yersinia pestis Species 0.000 title claims description 22
• RRZXIRBKKLTSOM-XPNPUAGNSA-N avermectin B1a Chemical class C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 RRZXIRBKKLTSOM-XPNPUAGNSA-N 0.000 title claims description 11
• 150000001875 compounds Chemical class 0.000 claims abstract description 342
• 125000001424 substituent group Chemical group 0.000 claims abstract description 131
• 125000003118 aryl group Chemical group 0.000 claims abstract description 40
• 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 40
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 33
• 150000002367 halogens Chemical class 0.000 claims abstract description 31
• 150000003839 salts Chemical group 0.000 claims abstract description 23
• 125000005844 heterocyclyloxy group Chemical group 0.000 claims abstract description 22
• 125000004104 aryloxy group Chemical group 0.000 claims abstract description 18
• 125000005110 aryl thio group Chemical group 0.000 claims abstract description 13
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims abstract description 11
• -1 - heterocyclyl Chemical group 0.000 claims description 89
• 150000002772 monosaccharides Chemical class 0.000 claims description 65
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
• 229910052739 hydrogen Inorganic materials 0.000 claims description 16
• 238000006467 substitution reaction Methods 0.000 claims description 15
• 229910052799 carbon Inorganic materials 0.000 claims description 10
• 239000012535 impurity Substances 0.000 claims description 9
• 125000000217 alkyl group Chemical group 0.000 claims description 8
• 125000002947 alkylene group Chemical group 0.000 claims description 7
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
• 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 4
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
• IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical class O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 claims description 4
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• 125000000304 alkynyl group Chemical group 0.000 claims description 4
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• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 9
• 229910052794 bromium Inorganic materials 0.000 description 9
• 239000000460 chlorine Substances 0.000 description 9
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