RU2554349C9 - N-(1,2,5-оксадиазол-3-ил)бензамиды и их применение в качестве гербицидов - Google Patents

Info

Publication number

RU2554349C9

RU2554349C9 RU2012111125/04A RU2012111125A RU2554349C9 RU 2554349 C9 RU2554349 C9 RU 2554349C9 RU 2012111125/04 A RU2012111125/04 A RU 2012111125/04A RU 2012111125 A RU2012111125 A RU 2012111125A RU 2554349 C9 RU2554349 C9 RU 2554349C9

Authority

RU

Russia

Prior art keywords

carbon atoms

alkyl

halogen

group

ome

Prior art date

2009-09-25

Links

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• 239000004009 herbicide Substances 0.000 title claims description 23
• RHLSTBAZUYRNTK-UHFFFAOYSA-N n-(1,2,5-oxadiazol-3-yl)benzamide Chemical class C=1C=CC=CC=1C(=O)NC=1C=NON=1 RHLSTBAZUYRNTK-UHFFFAOYSA-N 0.000 title abstract description 8
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 553
• -1 cyano, nitro, methylsulphenyl Chemical group 0.000 claims abstract description 492
• 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 296
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 158
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 46
• 150000002367 halogens Chemical class 0.000 claims abstract description 46
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 42
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 24
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 23
• 238000002360 preparation method Methods 0.000 claims abstract description 22
• 125000003342 alkenyl group Chemical group 0.000 claims abstract description 20
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 20
• 239000001257 hydrogen Substances 0.000 claims abstract description 20
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 18
• 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 16
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims abstract description 16
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 16
• 150000002431 hydrogen Chemical class 0.000 claims abstract description 14
• 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 13
• 125000003545 alkoxy group Chemical group 0.000 claims abstract description 12
• 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 12
• 125000003884 phenylalkyl group Chemical group 0.000 claims abstract description 10
• 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims abstract description 8
• 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 7
• 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims abstract description 6
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
• 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 claims abstract description 5
• 125000003226 pyrazolyl group Chemical group 0.000 claims abstract description 5
• 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 claims abstract description 3
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• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 5
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 5
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 5
• 125000001305 1,2,4-triazol-3-yl group Chemical group [H]N1N=C([*])N=C1[H] 0.000 claims description 3
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• 125000001506 1,2,3-triazol-5-yl group Chemical group [H]N1N=NC([H])=C1[*] 0.000 claims description 2
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• 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 23
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• 125000001607 1,2,3-triazol-1-yl group Chemical group [*]N1N=NC([H])=C1[H] 0.000 description 12
• VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 12
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
• 125000000896 monocarboxylic acid group Chemical group 0.000 description 12
• PAQZWJGSJMLPMG-UHFFFAOYSA-N 2,4,6-tripropyl-1,3,5,2$l^{5},4$l^{5},6$l^{5}-trioxatriphosphinane 2,4,6-trioxide Chemical compound CCCP1(=O)OP(=O)(CCC)OP(=O)(CCC)O1 PAQZWJGSJMLPMG-UHFFFAOYSA-N 0.000 description 11
• SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 description 11
• 239000011734 sodium Substances 0.000 description 11
• 229910052708 sodium Inorganic materials 0.000 description 11
• 239000000243 solution Substances 0.000 description 11
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