AR066040A1 - Derivados insecticidas de aminoheterociclos sustituidos - Google Patents
Derivados insecticidas de aminoheterociclos sustituidosInfo
- Publication number
- AR066040A1 AR066040A1 ARP080101513A AR066040A1 AR 066040 A1 AR066040 A1 AR 066040A1 AR P080101513 A ARP080101513 A AR P080101513A AR 066040 A1 AR066040 A1 AR 066040A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- halogen
- cyano
- nitro
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 23
- 229910052736 halogen Inorganic materials 0.000 abstract 21
- 150000002367 halogens Chemical group 0.000 abstract 21
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 20
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 20
- 125000003545 alkoxy group Chemical group 0.000 abstract 15
- 229910052739 hydrogen Inorganic materials 0.000 abstract 13
- 239000001257 hydrogen Substances 0.000 abstract 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 12
- 125000003342 alkenyl group Chemical group 0.000 abstract 7
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- -1 dialkylphosphonate Chemical group 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 2
- 229910052717 sulfur Chemical group 0.000 abstract 2
- 239000011593 sulfur Chemical group 0.000 abstract 2
- 241000238421 Arthropoda Species 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/28—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/08—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D277/12—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/18—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Abstract
La presente se refiere a nuevos derivados de aminoheterociclos, a procedimientos para su preparacion y a su uso para combatir plagas animales, en especial artropodos, en particular insectos. Reivindicacion 1: Compuestos de la formula (1) en la queA se selecciona de -CHR5-, -CHR5CHR6-, -O-, -S(O)n-, -NR7-, -OCHR5-, -CHR5O-, -S{O)nCHR5-, -CHR5S(O)n-, -C(X)- y C(=NOR7)-; B se selecciona de -CHR8-, -O- y -S(O)n-; X se seleccione de oxigeno y azufre; n es un numero entero seleccionado de 0, 1 y2; R, R1, R2 y R3 se seleccionan independientemente de hidrogeno, halogeno, hidroxi, alquilo, haloalquilo, alcoxi, haloalcoxi, alquiltio, haloalquiltio, alquenilo, haloalquenilo, alquinilo, ciano, nitro, arilo opcionalmente sustituido, ariloxiopcionalmente sustituido, heteroarilo opcionalmente sustituido, heteroariloxi opcionalmente sustituido, alcoxialquilo, alcoxialcoxialquilo. cicloalquilo, cianoalquilo, formilo, alcoxicarbonilo, alquilcarbonilo, alquenilcarbonilo, dialquilfosfonato,amino, monoalquilamino, dialquilamino, cicloalquilamino, (cicloalquil)(alquil)amino, sulfonilo, alquilsulfonilo, haloalquil-sulfonilo, alquilsulfinilo, alquilsulfinilalquilo, alquilsulfonilalquilo, alquilsulfoniloxi, halogeno-alquilsulfoniloxi,alquiltiocarbonilo y hidroxicarbonilo; Q se selecciona de (A),(B), (C), (D), (E), (F); R4 se toma junto con el átomo de conexion en Q formando un doble enlace como en (A), (B) y (C) o R4 se selecciona de hidrogeno, ciano, nitro, alquilo, alquenitoalquinilo, arialquilo, -C(X)R10, -C(X)OR11, -C(X)SR11, -S(O)nR11 y -C(X)NR11R12, R5 se selecciona de hidrogeno, halogeno, hidroxi, alquilo, alcoxi, alquiltio, haloalquilo, haloalcoxi, arilo, ciano y nitro; R6 se selecciona de hidrogeno, halogeno,hidroxi, alquilo, alcoxi, alquiltio, haloalquilo, haloalcoxi, arilo, ciano y nitro; R7 es hidrogeno o alquilo; R8 es hidrogeno, halogeno, alquilo, alcoxi y arilo, R9 se selecciona de -C(X)R13, -C(X)OR13, -C(X)SR13, -S(O)nR13, -C(X)NR13R14; -S(O)nNR13R14, -P(X)(OR13)(OR15) y P(X)(NR13R16)(NR17R18); R10 se selecciona de hidrogeno, alquilo y alquenilo; R11 y R12 se seleccionan independientemente de hidrogeno, alquilo, alquenilo y arilalquilo, R13 se seleccione de alquenilo (que él mismoestá opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), alquinilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo),arilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, oxialquilenoxi, S(O)n-alquilo y S(O)n-haloalquilo), heterociclilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro,alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), heteroarilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo); R14 se selecciona de hidrogeno, alquilo (que él mismoestá opcionalmente sustituido con halogeno, ciano, nitro, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), alquenilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), alquinilo(que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), arilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), heterociclilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), heteroarilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro,alquilo, alcoxi, S(O)n-alquilo y S(O)n-haloalquilo), R15 se selecciona de hidrogeno, alquilo, haloalquilo, alquenilo y arilalquilo; R16, R17 y R18 se seleccionan independientemente de hidrogeno, alquilo (que él mismo está opcionalmente sustituidocon halogeno, ciano, nitro, S(O)n-alquilo y S(O)n-haloalquilo), alquenilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, S(O)n-alquilo y S(O)n-haloalquilo), alquinilo (que él mismo está opcionalmente sustituido con halogeno,ciano, nitro, S(O)n-alquilo y S(O)n-haloalquilo), arilalquilo (que él mismo está opcionalmente sustituido con halogeno, ciano, nitro, S(O)n-alquilo y S(O)n-haloalquilo) y heterociclilalquilo (que él mismo está opcionalmente sustituido con halogeno,ciano, nitro, S(O)n-alquilo y S(O)n-haloalquilo); y R19 se selecciona de hidrogeno, halogeno y alquilo; y sus sales aceptables desde el punto de vista agrícola, con la condicion de que R13 no representa tetrahidrofurilmetilo cuando A se seleccionade -CHR5- y -CHR5CHR6- y B es -CHR8- y Q es (A) y R, R1, R2, R3, R5, R6, R8, R14 y R19 son hidrogeno y R9 es C(X)NR13R14 y X es azufre.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07007752A EP1982595A1 (en) | 2007-04-17 | 2007-04-17 | Insecticidal derivatives of substituted aminoheterocycles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR066040A1 true AR066040A1 (es) | 2009-07-22 |
Family
ID=39144464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080101513 AR066040A1 (es) | 2007-04-17 | 2008-04-11 | Derivados insecticidas de aminoheterociclos sustituidos |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1982595A1 (es) |
| AR (1) | AR066040A1 (es) |
| CL (1) | CL2008001018A1 (es) |
| TW (1) | TW200906811A (es) |
| WO (1) | WO2008125230A2 (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20070705A1 (es) * | 2005-11-25 | 2007-08-23 | Basf Ag | Compuestos de indanil - y tetrahidronaftil-amino-azolina para combatir pestes animales |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1963192A1 (de) * | 1969-12-17 | 1971-06-24 | Bayer Ag | Ektoparasiticide Mittel |
| GB0516706D0 (en) * | 2005-08-15 | 2005-09-21 | Syngenta Participations Ag | Chemical compounds |
| US8178567B2 (en) * | 2006-02-15 | 2012-05-15 | Fmc Corporation | Insecticidal substituted amino heterocyclic and heteroaryl derivatives |
| GB0615670D0 (en) * | 2006-08-07 | 2006-09-13 | Syngenta Participations Ag | Chemical compounds |
| BRPI0715136A2 (pt) * | 2006-08-07 | 2013-06-04 | Basf Se | uso de compostos, mÉtodos para o combate de insetos ou de pestes de nemÁtodos, de proteÇço de plantas e de semente, e para o tratamento, controle, prevenÇço ou proteÇço de animais contra a infestaÇço ou a infecÇço por endoparasitas, semente, compostos azolina, e, composiÇÕes |
-
2007
- 2007-04-17 EP EP07007752A patent/EP1982595A1/en not_active Withdrawn
-
2008
- 2008-04-04 WO PCT/EP2008/002678 patent/WO2008125230A2/en not_active Ceased
- 2008-04-10 CL CL2008001018A patent/CL2008001018A1/es unknown
- 2008-04-11 AR ARP080101513 patent/AR066040A1/es unknown
- 2008-04-16 TW TW97113722A patent/TW200906811A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW200906811A (en) | 2009-02-16 |
| WO2008125230A2 (en) | 2008-10-23 |
| EP1982595A1 (en) | 2008-10-22 |
| CL2008001018A1 (es) | 2008-10-24 |
| WO2008125230A3 (en) | 2010-05-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |