RU2656101C2 - Производные 1-(замещенный бензоил)-5-фтор-4-имино-3-метил-3,4-дигидропиримидин-2(1h)-она - Google Patents

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Publication number

RU2656101C2

RU2656101C2 RU2015131110A RU2015131110A RU2656101C2 RU 2656101 C2 RU2656101 C2 RU 2656101C2 RU 2015131110 A RU2015131110 A RU 2015131110A RU 2015131110 A RU2015131110 A RU 2015131110A RU 2656101 C2 RU2656101 C2 RU 2656101C2

Authority

RU

Russia

Prior art keywords

plant

compounds

compound

plants

compound according

Prior art date

2012-12-28

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• -1 1-(substituted benzoyl)-5-fluoro-4-imino-3-methyl-3,4-dihydropyrimidin-2(1h)-one Chemical class 0.000 title description 127
• 150000001875 compounds Chemical class 0.000 claims abstract description 123
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• 208000031888 Mycoses Diseases 0.000 claims abstract description 28
• 230000000855 fungicidal effect Effects 0.000 claims abstract description 20
• 206010017533 Fungal infection Diseases 0.000 claims abstract description 16
• 238000000034 method Methods 0.000 claims abstract description 16
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 15
• 150000003839 salts Chemical class 0.000 claims abstract description 15
• 239000002689 soil Substances 0.000 claims abstract description 13
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 10
• 241001360088 Zymoseptoria tritici Species 0.000 claims abstract description 10
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 7
• 241000530549 Cercospora beticola Species 0.000 claims abstract description 4
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• 241000228452 Venturia inaequalis Species 0.000 claims abstract description 4
• 241001065113 Cercosporidium Species 0.000 claims abstract description 3
• CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims abstract description 3
• 241001281801 Mycosphaerella arachidis Species 0.000 claims abstract description 3
• XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims abstract description 3
• 241000196324 Embryophyta Species 0.000 claims description 60
• 150000002367 halogens Chemical class 0.000 claims description 6
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• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
• 229910052801 chlorine Inorganic materials 0.000 claims description 4
• 150000004677 hydrates Chemical class 0.000 claims description 4
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
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• ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 4
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• 235000015112 vegetable and seed oil Nutrition 0.000 description 4
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• ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 3
• LJLWZAAOVUNDHM-UHFFFAOYSA-N 4-amino-5-fluoro-1-(4-methoxyphenyl)sulfonylpyrimidin-2-one Chemical compound C1=CC(OC)=CC=C1S(=O)(=O)N1C(=O)NC(=N)C(F)=C1 LJLWZAAOVUNDHM-UHFFFAOYSA-N 0.000 description 3
• MGBHNKWOVQDGIB-UHFFFAOYSA-N 5-fluoro-4-imino-1-(4-methoxyphenyl)sulfonyl-3-methylpyrimidin-2-one Chemical compound C1=CC(OC)=CC=C1S(=O)(=O)N1C(=O)N(C)C(=N)C(F)=C1 MGBHNKWOVQDGIB-UHFFFAOYSA-N 0.000 description 3
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
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• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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