ECSP993093A - NEMATICIDAL PRAZOLES - Google Patents
NEMATICIDAL PRAZOLESInfo
- Publication number
- ECSP993093A ECSP993093A ECSP993093A ECSP993093A EC SP993093 A ECSP993093 A EC SP993093A EC SP993093 A ECSP993093 A EC SP993093A EC SP993093 A ECSP993093 A EC SP993093A
- Authority
- EC
- Ecuador
- Prior art keywords
- carbons
- total number
- alkyl
- optionally substituted
- total
- Prior art date
Links
- 230000001069 nematicidal effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 1
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 1
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 230000000507 anthelmentic effect Effects 0.000 abstract 1
- 239000000921 anthelmintic agent Substances 0.000 abstract 1
- 229940124339 anthelmintic agent Drugs 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000005645 nematicide Substances 0.000 abstract 1
- 150000003217 pyrazoles Chemical class 0.000 abstract 1
Landscapes
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Nuevos pirazoles de fórmula I (gráfico), en donde: R1 representa halógeno, alquilo C1-6 haloalquilo C1-5, alcoxi C2-6, alquiltio C1-4, alqueniloxi C2-5, alquiniloxi C3-5, alcoxialquilo C2-6 (número total de carbonos), alquitioalquilo C2-6 (número total de carbonos), haloalcoxi C1-5, alcoxialcoxi C2-6 (número total de carbonos), hidroxi o fenilo opcionalemente sustituido; R2 representa hidrógeno, halógeno, alquilo C1-5, alcoxialquilo C2-6 (número total de carbonos), alquiltioalquilo C2-6 (número total de carbonos), alquilsulfinilalquilo C2-6 (número total de carbonos), alquilsulfonilalquilo C2-6 (número total de carbonos), o haloalquilo C1-5; R3 representa hidrógeno, alquilo C1-5 -COR4, -COOR5, CH(OR6)2 o CH2Si(R7)3; R4 representa alquilo C1-10, haloalquilo C1-6, alquenilo C2-6, cicloalquilo C3-6 opcionalemnte sustituido, alcoxialquilo C2-6 (número total de carbonos), alquiltioalquilo C2-6 (número total de carbonos), fenilo opcionalmente sustituido, alquilamino C1-5, di-(alquil C1-6) amino o fenilamino opcionalmente sustituido; R5 representa alquilo C1-7; R6 y R7 representan alquilo C1-6; y n es 1,2 ó 3 y cuando n es 2 ó 3, el correspondiente número (n) de radicales R1 puede ser igual o diferente; procedimientos para la preparación de estos compuestos y su uso como nematicidas y antihelmínticos.Novel pyrazoles of formula I (graph), wherein: R1 represents halogen, C1-6alkyl, C1-5alkyl, C2-6alkoxy, C1-4alkylthio, C2-5alkenyloxy, C2-6alkoxyalkyl ( total carbon number), C2-6 alkythioalkyl (total number of carbons), C1-5 haloalkoxy, C2-6 alkoxyalkoxy (total number of carbons), hydroxy or optionally substituted phenyl; R2 represents hydrogen, halogen, C1-5 alkyl, C2-6 alkoxyalkyl (total number of carbons), C2-6 alkylthioalkyl (total number of carbons), alkylsulfinylalkyl C2-6 (total number of carbons), alkylsulfonylalkyl C2-6 (number total carbons), or C1-5 haloalkyl; R3 represents hydrogen, C1-5 alkyl -COR4, -COOR5, CH (OR6) 2 or CH2Si (R7) 3; R4 represents C1-10 alkyl, C1-6 haloalkyl, C2-6 alkenyl, optionally substituted C3-6 cycloalkyl, C2-6 alkoxyalkyl (total number of carbons), C2-6 alkylthioalkyl (total number of carbons), optionally substituted phenyl, optionally substituted C1-5alkylamino, di- (C1-6alkyl) amino or phenylamino; R5 represents C1-7 alkyl; R6 and R7 represent C1-6 alkyl; and n is 1,2 or 3 and when n is 2 or 3, the corresponding number (n) of radicals R1 can be the same or different; procedures for the preparation of these compounds and their use as nematicides and anthelmintics.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP993093 ECSP993093A (en) | 1999-08-10 | 1999-08-10 | NEMATICIDAL PRAZOLES |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP993093 ECSP993093A (en) | 1999-08-10 | 1999-08-10 | NEMATICIDAL PRAZOLES |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP993093A true ECSP993093A (en) | 1999-11-29 |
Family
ID=42044080
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSP993093 ECSP993093A (en) | 1999-08-10 | 1999-08-10 | NEMATICIDAL PRAZOLES |
Country Status (1)
| Country | Link |
|---|---|
| EC (1) | ECSP993093A (en) |
-
1999
- 1999-08-10 EC ECSP993093 patent/ECSP993093A/en unknown
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