BRPI0316993B1 - derivados de 5-(acilamino)pirazol pesticidas - Google Patents

Info

Publication number

BRPI0316993B1

BRPI0316993B1 BRPI0316993A BR0316993A BRPI0316993B1 BR PI0316993 B1 BRPI0316993 B1 BR PI0316993B1 BR PI0316993 A BRPI0316993 A BR PI0316993A BR 0316993 A BR0316993 A BR 0316993A BR PI0316993 B1 BRPI0316993 B1 BR PI0316993B1

Authority

BR

Brazil

Prior art keywords

alkyl

haloalkyl

compound

substituted

group

Prior art date

2002-12-03

Links

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• 239000000575 pesticide Substances 0.000 title abstract description 10
• 125000004442 acylamino group Chemical group 0.000 title abstract description 3
• 150000003217 pyrazoles Chemical class 0.000 title 1
• 239000000203 mixture Substances 0.000 claims abstract description 90
• 150000003839 salts Chemical class 0.000 claims abstract description 39
• 238000000034 method Methods 0.000 claims abstract description 37
• 241000607479 Yersinia pestis Species 0.000 claims abstract description 35
• 150000001875 compounds Chemical class 0.000 claims description 157
• -1 (C2 -C6) - haloalkyl Chemical group 0.000 claims description 61
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 50
• 229910052736 halogen Inorganic materials 0.000 claims description 36
• 150000002367 halogens Chemical class 0.000 claims description 36
• 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims description 31
• XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 23
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 23
• 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 20
• 125000001188 haloalkyl group Chemical group 0.000 claims description 19
• 229910052717 sulfur Inorganic materials 0.000 claims description 19
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 18
• 229910052760 oxygen Inorganic materials 0.000 claims description 17
• 125000000217 alkyl group Chemical group 0.000 claims description 16
• 125000001424 substituent group Chemical group 0.000 claims description 15
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
• 229910052757 nitrogen Inorganic materials 0.000 claims description 13
• 125000005842 heteroatom Chemical group 0.000 claims description 12
• 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 11
• 238000002360 preparation method Methods 0.000 claims description 11
• 229920006395 saturated elastomer Polymers 0.000 claims description 11
• 239000004094 surface-active agent Substances 0.000 claims description 11
• 229910052721 tungsten Inorganic materials 0.000 claims description 11
• 125000000623 heterocyclic group Chemical group 0.000 claims description 10
• 229910052739 hydrogen Inorganic materials 0.000 claims description 10
• 239000001257 hydrogen Substances 0.000 claims description 10
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 9
• 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 9
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 8
• 230000000361 pesticidal effect Effects 0.000 claims description 8
• 229910052799 carbon Inorganic materials 0.000 claims description 7
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
• 125000006536 (C1-C2)alkoxy group Chemical group 0.000 claims description 6
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 6
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• 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 6
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 6
• 125000003342 alkenyl group Chemical group 0.000 claims description 6
• 125000003545 alkoxy group Chemical group 0.000 claims description 6
• 239000003085 diluting agent Substances 0.000 claims description 6
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
• 125000004076 pyridyl group Chemical group 0.000 claims description 6
• 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims description 5
• 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 5
• 125000003118 aryl group Chemical group 0.000 claims description 5
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
• 125000006413 ring segment Chemical group 0.000 claims description 5
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