RU98107574A - PIRAZIN-2-ONE DERIVATIVES, THEIR APPLICATION AND INTERMEDIATE COMPOUNDS FOR THEIR PRODUCTION - Google Patents
PIRAZIN-2-ONE DERIVATIVES, THEIR APPLICATION AND INTERMEDIATE COMPOUNDS FOR THEIR PRODUCTIONInfo
- Publication number
- RU98107574A RU98107574A RU98107574/04A RU98107574A RU98107574A RU 98107574 A RU98107574 A RU 98107574A RU 98107574/04 A RU98107574/04 A RU 98107574/04A RU 98107574 A RU98107574 A RU 98107574A RU 98107574 A RU98107574 A RU 98107574A
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- Prior art keywords
- alkyl
- compounds
- hydrogen
- carbonyl
- alkoxy
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims 40
- 125000000217 alkyl group Chemical group 0.000 claims 64
- 229910052739 hydrogen Inorganic materials 0.000 claims 25
- 239000001257 hydrogen Substances 0.000 claims 25
- 125000003545 alkoxy group Chemical group 0.000 claims 21
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 18
- -1 chlorosulfonyl Chemical group 0.000 claims 13
- 150000002431 hydrogen Chemical group 0.000 claims 13
- 125000000304 alkynyl group Chemical group 0.000 claims 10
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- 239000001301 oxygen Substances 0.000 claims 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 125000001188 haloalkyl group Chemical group 0.000 claims 5
- 201000002674 obstructive nephropathy Diseases 0.000 claims 5
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 125000000262 haloalkenyl group Chemical group 0.000 claims 4
- 229910052736 halogen Chemical group 0.000 claims 4
- 150000002367 halogens Chemical group 0.000 claims 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 3
- 239000000460 chlorine Chemical group 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 3
- 125000000232 haloalkynyl group Chemical group 0.000 claims 3
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 239000011593 sulfur Substances 0.000 claims 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 claims 2
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims 2
- 125000004849 alkoxymethyl group Chemical group 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 230000002363 herbicidal Effects 0.000 claims 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 1
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000003302 alkenyloxy group Chemical group 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 claims 1
- 0 Cc1c(*)cc(*)c2c1CC(*)*2 Chemical compound Cc1c(*)cc(*)c2c1CC(*)*2 0.000 description 1
Claims (37)
в которой R1 обозначает водород или C1 - C3 алкил; R2 обозначает C1 - C3 галогеналкил; R3 обозначает C1 - C6 алкил, необязательно замещенный одним или несколькими атомами галогена; C3 - C6 алкенил или C3 - C6 алкинил; и Q обозначает необязательно замещенный фенил.1. Compounds of the formula:
in which R 1 denotes hydrogen or C 1 - C 3 alkyl; R 2 is C 1 -C 3 haloalkyl; R 3 is C 1 -C 6 alkyl optionally substituted with one or more halogen atoms; C 3 - C 6 alkenyl or C 3 - C 6 alkynyl; and Q is optionally substituted phenyl.
где X обозначает водород или галоген;
Y обозначает галоген, нитро, циано или трифторметил;
Z1 обозначает кислород, серу, NH или метилен;
Z2 обозначает кислород или серу;
n равен 0 или 1;
B обозначает водород, галоген, нитро, циано, хлорсульфонил, -OR10, -SR10, -SO2OR10, -N(R10)R11, -SO2N(R11)R12, -NR11(COR13), -NR11(SO2R14), -N(SO2R14)(SO2R15), -N(SO2R14)(COR13), -NR11(COOR13), -COOR13, -CON(R11)R12, -CSN(R11)R12, -COR16, -CR17=CR18CHO, -CR17=CR18COOR10, -CR17= CR18CON(R11)R12, -CH2CHWCOOR13 или -CH2CHWCON(R11)R12;
R4 обозначает водород или C1 - C3 алкил;
R5 обозначает водород, C1 - C6 алкил, C1 - C6 галогеналкил, C3 - C6 алкенил, C3 - C6 галогеналкенил, C3 - C6 алкинил, C3 - C6 галогеналкинил, циано C1 - C6 алкил, C2 - C8 алкоксиалкил, C3 - C8 алкоксиалкоксиалкил, карбокси C1 - C6 алкил, (C1 - C6 алкокси) карбонил C1 - C6 алкил, {(C1 - C4 алкокси) C1 - C4 алкокси} карбонил C1 - C6 алкил, (C3 - C8 циклоалкокси) карбонил C1 - C6 алкил, CH2CON(R11)R12, -CH2COON(R11)R12, -CH(C1 - C4 алкил) CON(R11)R12, -CH(C1 - C4 алкил) COON(R11)R12, C2 - C8 алкилтиоалкил, C1 - C6 алкилсульфонил, C1 - C6 галогеналкилсульфонил, (C1 - C8 алкил) карбонил, (C1 - C8 алкокси) карбонил или гидрокси C1 - C6 алкил;
R6 обозначает C1 - C6 алкил, C1 - C6 галогеналкил, формил, циано, карбоксил, гидрокси C1 - C6 алкил, C1 - C6 алкокси C1 - C6 алкил, C1 - C6 алкокси C1 - C6 алкокси C1 - C6 алкил, (C1 - C6 алкил) карбонилокси C1 - C6 алкил, (C1 - C6 галогеналкил) карбонилокси C1 - C6 алкил, (C1 - C6 алкокси) карбонил или (C1 - C6 алкил) карбонил;
R7 обозначает водород или C1 - C3 алкил; и
R8 обозначает C1 - C6 алкил, C1 - C6 галогеналкил, гидрокси C1 - C6, алкил, C2 - C8 алкоксиалкил, C3 - C10 алкоксиалкоксиалкил, (C1 - C5 алкил) карбонилокси C1 - C6 алкил, (C1 - C6 галогеналкил) карбонилокси C1 - C6 алкил, карбоксил, карбокси C1 - C6 алкил, (C1 - C8 алкокси) карбонил, (C1 - C6 галогеналкокси) карбонил, (C3 - C10 циклоалкокси) карбонил, (C3 - C8 алкенилокси) карбонил, (C3 - C8 алкинилокси) карбонил, аминокарбонил, (C1 - C6 алкил) аминокарбонил, ди (C1 - C6 алкил)аминокарбонил, (C1 - C6 алкил) аминокарбонилокси C1 - C6 алкил или ди (C1 - C6 алкил)аминокарбонилокси C1 - C6 алкил;
где W обозначает водород, хлор или бром;
R10 обозначает водород, C1 - C6 алкил, C1 - C6 галогеналкил, C3 - C8 циклоалкил, C3 - C6 алкенил, C3 - C6 галогеналкенил, C3 - C6 алкинил, C3 - C6 галогеналкинил, циано C1 - C6алкил, C2 - C8 алкоксиалкил, C2 - C8 алкилтиоалкил, карбокси C1 - C6алкил, (C1 - C6 алкокси) карбонил C1 - C6 алкил, { (C1 - C4 алкокси) C1 - C4 алкокси} карбонил C1 - C6 алкил, (C3 - C8 циклоалкокси) карбонил C1 - C6 алкил, -CH2CON(R11)R12, -CH2COON(R11)R12, -CH(C1 - C4 алкил) CON(R11)R12 или -CH(C1 - C4 алкил) COON(R11)R12;
R11 и R12 независимо друг от друга обозначают водород, C1 - C6 алкил, C1 - C6 галогеналкил, C3 - C6 алкенил, C3 - C6 алкинил, циано C1 - C6 алкил, C2 - C8 алкоксиалкил, C2 - C8 алкилтиоалкил, карбокси C1 - C6 алкил, (C1 - C6 алкокси) карбонил C1 - C6 алкил или {(C1 - C4 алкокси) C1 - C4 алкокси} карбонил C1 - C алкил, либо R11 и R12, вместе взятые, образуют тетраметилен, пентаметилен или этиленоксиэтилен;
R13 обозначает водород, C1 - C6 алкил, C1 - C6 галогеналкил или C3 - C8 циклоалкил;
R14 и R15 независимо друг от друга обозначают C1 - C6 алкил, C1 - C6 галогеналкил или фенил, необязательно замещенный метилом или нитро;
R16 обозначает водород, C1 - C6 алкил, C1 - C6 галогеналкил, C2 - C6 алкенил, C2 - C6 галогеналкенил, C2 - C6 алкинил, C2 - C6 галогеналкинил, C2 - C8 алкоксиалкил или гидрокси C1 - C6 алкил; и
R17 и R18 независимо друг от друга обозначают водород или C1 - C6 алкил.2. The compounds according to claim 1, in which Q represents the group [Q - 1], [Q - 2], [Q - 3], [Q - 4] or [Q - 5] of the formula:
where X is hydrogen or halogen;
Y is halogen, nitro, cyano or trifluoromethyl;
Z 1 is oxygen, sulfur, NH or methylene;
Z 2 is oxygen or sulfur;
n is 0 or 1;
B is hydrogen, halogen, nitro, cyano, chlorosulfonyl, -OR 10 , -SR 10 , -SO 2 OR 10 , -N (R 10 ) R 11 , -SO 2 N (R 11 ) R 12 , -NR 11 ( COR 13 ), -NR 11 (SO 2 R 14 ), -N (SO 2 R 14 ) (SO 2 R 15 ), -N (SO 2 R 14 ) (COR 13 ), -NR 11 (COOR 13 ), -COOR 13 , -CON (R 11 ) R 12 , -CSN (R 11 ) R 12 , -COR 16 , -CR 17 = CR 18 CHO, -CR 17 = CR 18 COOR 10 , -CR 17 = CR 18 CON (R 11 ) R 12 , -CH 2 CHWCOOR 13 or -CH 2 CHWCON (R 11 ) R 12 ;
R 4 is hydrogen or C 1 -C 3 alkyl;
R 5 is hydrogen, C 1 - C 6 alkyl, C 1 - C 6 haloalkyl, C 3 - C 6 alkenyl, C 3 - C 6 haloalkenyl, C 3 - C 6 alkynyl, C 3 - C 6 haloalkynyl, cyano C 1 - C 6 alkyl, C 2 - C 8 alkoxyalkyl, C 3 - C 8 alkoxyalkoxyalkyl, carboxy C 1 - C 6 alkyl, (C 1 - C 6 alkoxy) carbonyl C 1 - C 6 alkyl, {(C 1 - C 4 alkoxy) C 1 - C 4 alkoxy} carbonyl C 1 - C 6 alkyl, (C 3 - C 8 cycloalkoxy) carbonyl C 1 - C 6 alkyl, CH 2 CON (R 11 ) R 12 , -CH 2 COON (R 11 ) R 12 , -CH (C 1 - C 4 alkyl) CON (R 11 ) R 12 , -CH (C 1 - C 4 alkyl) COON (R 11 ) R 12 , C 2 - C 8 alkylthioalkyl, C 1 - C 6 alkylsulfonyl, C 1 - C 6 haloalkylsulfonyl, (C 1 - C 8 alkyl) carbonyl, (C 1 - C 8 alkoxy) carbonyl or hydroxy C 1 - C 6 alkyl;
R 6 is C 1 - C 6 alkyl, C 1 - C 6 haloalkyl, formyl, cyano, carboxyl, hydroxy C 1 - C 6 alkyl, C 1 - C 6 alkoxy C 1 - C 6 alkyl, C 1 - C 6 alkoxy C 1 - C 6 alkoxy C 1 - C 6 alkyl, (C 1 - C 6 alkyl) carbonyloxy C 1 - C 6 alkyl, (C 1 - C 6 haloalkyl) carbonyloxy C 1 - C 6 alkyl, (C 1 - C 6 alkoxy) carbonyl or (C 1 - C 6 alkyl) carbonyl;
R 7 is hydrogen or C 1 -C 3 alkyl; and
R 8 is C 1 - C 6 alkyl, C 1 - C 6 haloalkyl, hydroxy C 1 - C 6 , alkyl, C 2 - C 8 alkoxyalkyl, C 3 - C 10 alkoxyalkoxyalkyl, (C 1 - C 5 alkyl) carbonyloxy C 1 - C 6 alkyl, (C 1 - C 6 haloalkyl) carbonyloxy C 1 - C 6 alkyl, carboxyl, carboxy C 1 - C 6 alkyl, (C 1 - C 8 alkoxy) carbonyl, (C 1 - C 6 haloalkoxy) carbonyl, (C 3 - C 10 cycloalkoxy) carbonyl, (C 3 - C 8 alkenyloxy) carbonyl, (C 3 - C 8 alkynyloxy) carbonyl, aminocarbonyl, (C 1 - C 6 alkyl) aminocarbonyl, di (C 1 - C 6 alkyl) aminocarbonyl, (C 1 - C 6 alkyl) aminocarbonyloxy C 1 - C 6 alkyl or di (C 1 - C 6 alkyl) aminocarbonyloxy C 1 - C 6 alkyl;
where W is hydrogen, chlorine or bromine;
R 10 is hydrogen, C 1 is C 6 alkyl, C 1 is C 6 haloalkyl, C 3 is C 8 cycloalkyl, C 3 is C 6 alkenyl, C 3 is C 6 haloalkenyl, C 3 is C 6 alkynyl, C 3 is C 6 haloalkynyl, cyano C 1 - C 6 alkyl, C 2 - C 8 alkoxyalkyl, C 2 - C 8 alkylthioalkyl, carboxy C 1 - C 6 alkyl, (C 1 - C 6 alkoxy) carbonyl C 1 - C 6 alkyl, {(C 1 - C 4 alkoxy) C 1 - C 4 alkoxy} carbonyl C 1 - C 6 alkyl, (C 3 - C 8 cycloalkoxy) carbonyl C 1 - C 6 alkyl, -CH 2 CON (R 11 ) R 12 , -CH 2 COON (R 11 ) R 12 , -CH (C 1 - C 4 alkyl) CON (R 11 ) R 12 or -CH (C 1 - C 4 alkyl) COON (R 11 ) R 12 ;
R 11 and R 12 are independently hydrogen, C 1 - C 6 alkyl, C 1 - C 6 haloalkyl, C 3 - C 6 alkenyl, C 3 - C 6 alkynyl, cyano C 1 - C 6 alkyl, C 2 - C 8 alkoxyalkyl, C 2 - C 8 alkylthioalkyl, carboxy C 1 - C 6 alkyl, (C 1 - C 6 alkoxy) carbonyl C 1 - C 6 alkyl or {(C 1 - C 4 alkoxy) C 1 - C 4 alkoxy} carbonyl C 1 -C alkyl, or R 11 and R 12 taken together form tetramethylene, pentamethylene or ethyleneoxyethylene;
R 13 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 3 -C 8 cycloalkyl;
R 14 and R 15 are independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or phenyl optionally substituted with methyl or nitro;
R 16 is hydrogen, C 1 is C 6 alkyl, C 1 is C 6 haloalkyl, C 2 is C 6 alkenyl, C 2 is C 6 haloalkenyl, C 2 is C 6 alkynyl, C 2 is C 6 haloalkynyl, C 2 is C 8 alkoxyalkyl or hydroxy C 1 -C 6 alkyl; and
R 17 and R 18 are independently hydrogen or C 1 -C 6 alkyl.
Y обозначает галоген;
Z1 обозначает кислород или серу;
Z2 обозначает кислород;
B обозначает водород, нитро, -OR10, -SR10, -NHR10, -NHSO2R14, -COOR13 или -CH2CHWCOOR13;
R5 обозначает C1 - C6 алкил, C3 - C6 алкенил или C3 - C6 алкинил;
R6 обозначает C1 - C6 алкил, C1 - C6 галогеналкил, формил, гидроксиметил, C1 - C6 алкоксиметил, C1 - C6 алкилкарбонилоксиметил или C1 - C6 алкоксикарбонил;
R7 обозначает водород или метил; и
R8 обозначает метил, гидроксиметил, C1 - C6 алкоксиметил, (C1 - C5 алкил) карбонилоксиметил, карбоксил или (C1 - C6 алкокси) карбонил;
где W обозначает водород или хлор;
R10 обозначает C1 - C6 алкил, C3 - C8 циклоалкил, C3 - C6 алкенил, C3 - C6 галогеналкенил, C3 - C6 алкинил, циано C1 - C6 алкил или (C1 - C6 алкокси) карбонил C1 - C6 алкил;
R13 обозначает C1 - C6 алкил; и
R14 обозначает C1 - C6 алкил.3. The compounds according to claim 2, in which Q denotes [Q - 1], [Q - 2], [Q - 3] or [Q - 4];
Y is halogen;
Z 1 is oxygen or sulfur;
Z 2 is oxygen;
B is hydrogen, nitro, —OR 10 , —SR 10 , —NHR 10 , —NHSO 2 R 14 , —COOR 13, or —CH 2 CHWCOOR 13 ;
R 5 is C 1 -C 6 alkyl, C 3 -C 6 alkenyl or C 3 -C 6 alkynyl;
R 6 is C 1 –C 6 alkyl, C 1 –C 6 haloalkyl, formyl, hydroxymethyl, C 1 –C 6 alkoxymethyl, C 1 –C 6 alkylcarbonyloxymethyl or C 1 –C 6 alkoxycarbonyl;
R 7 is hydrogen or methyl; and
R 8 is methyl, hydroxymethyl, C 1 –C 6 alkoxymethyl, (C 1 –C 5 alkyl) carbonyloxymethyl, carboxyl or (C 1 –C 6 alkoxy) carbonyl;
where W is hydrogen or chlorine;
R 10 is C 1 - C 6 alkyl, C 3 - C 8 cycloalkyl, C 3 - C 6 alkenyl, C 3 - C 6 haloalkenyl, C 3 - C 6 alkynyl, cyano C 1 - C 6 alkyl or (C 1 - C 6 alkoxy) carbonyl C 1 - C 6 alkyl;
R 13 is C 1 -C 6 alkyl; and
R 14 is C 1 -C 6 alkyl.
где R1 обозначает водород или C1 - C3 алкил; R2 обозначает C1 - C3 галогеналкил и Q обозначает необязательно замещенный фенил, с соединением формулы:
R3 - D [3]
где R3 обозначает C1 - C6 алкил, необязательно замещенный одним или несколькими атомами галогена; C3 - C6 алкенил или C3 - C6 алкинил; D обозначает хлор, бром, иод, метансульфонилокси, трифторметансульфонилокси или п-толуолсульфонилокси.29. The method of producing compounds according to claim 1, which includes the interaction of a compound of the formula:
where R 1 denotes hydrogen or C 1 - C 3 alkyl; R 2 is C 1 -C 3 haloalkyl and Q is optionally substituted phenyl, with a compound of the formula:
R 3 - D [3]
wherein R 3 is C 1 -C 6 alkyl optionally substituted with one or more halogen atoms; C 3 - C 6 alkenyl or C 3 - C 6 alkynyl; D is chloro, bromo, iodo, methanesulfonyloxy, trifluoromethanesulfonyloxy or p-toluenesulfonyloxy.
в которой R1 обозначает водород или C1 - C3 алкил, R2 обозначает C1 - C3 галогеналкил и Q обозначает необязательно замещенный фенил.33. Compounds of the formula:
wherein R 1 is hydrogen or C 1 -C 3 alkyl, R 2 is C 1 -C 3 haloalkyl, and Q is optionally substituted phenyl.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7/244107 | 1995-09-22 | ||
JP8/123566 | 1996-05-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
RU98107574A true RU98107574A (en) | 2000-02-10 |
Family
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