AR049391A1 - Derivados de aminoacetonitrilo y su uso para controlar parasitos en animales de sangre caliente - Google Patents
Derivados de aminoacetonitrilo y su uso para controlar parasitos en animales de sangre calienteInfo
- Publication number
- AR049391A1 AR049391A1 ARP050102344A ARP050102344A AR049391A1 AR 049391 A1 AR049391 A1 AR 049391A1 AR P050102344 A ARP050102344 A AR P050102344A AR P050102344 A ARP050102344 A AR P050102344A AR 049391 A1 AR049391 A1 AR 049391A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- mono
- poly
- unsubstituted
- halogen
- Prior art date
Links
- 241001465754 Metazoa Species 0.000 title abstract 2
- 244000045947 parasite Species 0.000 title abstract 2
- 150000008361 aminoacetonitriles Chemical class 0.000 title 1
- 239000008280 blood Substances 0.000 title 1
- 210000004369 blood Anatomy 0.000 title 1
- -1 carboxy, aminocarbonyl Chemical group 0.000 abstract 22
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical class 0.000 abstract 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical class 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 2
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 2
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000005136 alkenylsulfinyl group Chemical group 0.000 abstract 2
- 125000005137 alkenylsulfonyl group Chemical group 0.000 abstract 2
- 125000005108 alkenylthio group Chemical group 0.000 abstract 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 2
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000003236 benzoyl group Chemical class [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 2
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 2
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 2
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 2
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004664 haloalkylsulfonylamino group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- 125000005554 pyridyloxy group Chemical class 0.000 abstract 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 1
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- DFNYGALUNNFWKJ-UHFFFAOYSA-N aminoacetonitrile Chemical compound NCC#N DFNYGALUNNFWKJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 1
- 125000005142 aryl oxy sulfonyl group Chemical class 0.000 abstract 1
- 125000004657 aryl sulfonyl amino group Chemical class 0.000 abstract 1
- 125000005279 aryl sulfonyloxy group Chemical class 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 125000004426 substituted alkynyl group Chemical group 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/62—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
- C07C255/26—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups, amino groups and singly-bound oxygen atoms bound to the carbon skeleton
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La presente se refiere a compuestos derivados de aminoacetonitrilo donde los ingredientes activos tienen propiedades pesticidas ventajosas. Son particularmente adecuados para controlar parásitos en animales de sangre caliente. Reivindicacion 1: Un compuesto de la formula (1), en donde: Ar es arilo o hetarilo no sustituido o mono- o poli-sustituido; R1 es hidrogeno, alquilo C1-6, haloalquilo C1-6, alquilcarbonilo C1-6, alcoxicarbonilo C1-6, alilo, alcoximetilo C1-6, fenilcarbonilo no sustituido o mono- o poli-sustituido, alquilsulfonilo C1-6 o fenilsulfonilo no sustituido o mono- o poli-sustituido; R2, R3, R4, R5 y R6 son ya sea, independientemente uno del otro, hidrogeno, halogeno, alquilo C1-6 no sustituido o mono- o poli- sustituido, alquenilo C2-6 no sustituido o mono- o poli-sustituido, alquinilo C2-6 no sustituido o mono- o poli-sustituido, alcoxi C1-6 no sustituido o mono- o poli-sustituido, por lo que los sustituyentes en cada caso pueden ser independientes uno del otro y se seleccionan del grupo que consiste de halogeno, alcoxi C1-6 y haloalcoxi C1-6; cicloalquilo C3-6 no sustituido o mono- o poli-sustituido, por lo que los sustituyentes en cada caso pueden ser independientes uno del otro y se seleccionan del grupo que consiste en halogeno y alquilo C1-6; fenilo no sustituido o mono- o poli-sustituido, por lo que los sustituyentes en cada caso pueden ser independientes uno del otro y se seleccionan del grupo que consiste de halogeno, nitro, ciano, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, haloalquiltio C1-6, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, alquilamino C1-6 y dialquilamino C1-6; o R2 y R3 son en conjunto alquileno C2-6; R7 y R10 son, independientemente uno del otro, NH2, OH, SH, carboxi, aminocarbonilo, aminotiocarbonilo, aminotiocarboniloxi, ureilo, tioureilo, feniltiocarbamido no sustituido o mono- o poli-sustituido, alquiltiocarbamido C1- 6 no sustituido o mono- o poli-sustituido, alcoxitiocarbamido C1-6 no sustituido o mono- o poli-sustituido, feniloxitiocarbamido no sustituido o mono- o poli-sustituido, fenilaminotiocarboxi no sustituido o mono- o poli-sustituido, feniloxitiocarboxi no sustituido o mono- o poli-sustituido, fenilaminotiocarboxamido no sustituido o mono- o poli-sustituido, alquilaminotiocarbonilo C1-6 no sustituido o mono- o poli-sustituido, (alquilo C1-6)2aminotiocarbonilo, fenilaminotiocarbonilo, fenilsulfanilcarbonilo no sustituido o mono- o poli-sustituido, bencilsulfanilcarbonilo no sustituido o mono- o poli-sustituido, fenilsulfanilalquilo C1-6 no sustituido o mono- o poli-sustituido, fenilalquilsulfanilo C1-6 no sustituido o mono- o poli-sustituido, alquilsulfanilcarbonilo C1-6, alquilcarbonilsulfanilo C1-6, fenilcarbonilsulfanilo no sustituido o mono- o poli-sustituido, haloalquinilo C2-6, alquilaminotiocarboxi C1-6, alquiloxitiocarboxi C1-6, alquilaminotiocarboxamido C1-6, (1,3)-oxatiolilo, 2-halo-(1,3)-oxatiolilo, (1,3)-dioxolilo, 2-halo-(1,3)-dioxolilo, sulfonilo, aminosulfonilo, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C1-6, arilaminosulfonilo no sustituido o mono- o poli- sustituido, arilsulfoniloxi no sustituido o mono- o poli-sustituido, arilsulfonilamino no sustituido o mono- o poli-sustituido, ariloxisulfonilo no sustituido o mono- o poli-sustituido, alquiloxisulfonilo C1-6, alquilaminocarbonilsulfanilo C1-6, fenilaminocarbonilsulfanilo no sustituido o mono- o poli-sustituido, fenoxitiocarbonilo no sustituido o mono- o poli-sustituido, fenilsulfaniltiocarbonilo no sustituido o mono- o poli-sustituido, o alquiloxitiocarbonilo C1-6, en donde los sustituyentes en cada caso pueden ser independientes uno del otro y se seleccionan del grupo que consiste de R1 y halogeno; R8 es halogeno, nitro, ciano, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, haloalquenilo C2- 6, alquinilo C2-6, cicloalquilo C3-6, cicloalcoxi C3-6, cicloalquilamino C3-6, cicloalquiltio C3-6, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiltio C1-6, haloalquiltio C1-6, alquilsulfoniloxi C1-6, haloalquilsulfoniloxi C1-6, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, alqueniltio C2-6, haloalqueniltio C2-6, alquenilsulfinilo C2-6, haloalquenilsulfinilo C2-6, alquenilsulfonilo C2-6, haloalquenilsulfonilo C2-6, alquilamino C1-6, dialquilamino C1-6, alquilsulfonilamino C1-6, haloalquilsulfonilamino C1-6, alquilcarbonilo C1-6, haloalquilcarbonilo C1-6, alcoxicarbonilo C1-6, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, fenilamino no sustituido o mono- o poli-sustituido, fenilcarbonilo no sustituido o mono- o poli-sustituido, fenilmetoximino no sustituido o mono- o poli-sustituido, fenilhidroximetilo no sustituido o mono- o poli-sustituido, 1-fenil-1-hidroxietilo no sustituido o mono- o poli-sustituido, fenilclorometilo no sustituido o mono- o poli-sustituido, fenilcianometilo no sustituido o mono- o poli-sustituido, fenilo no sustituido o mono- o poli-sustituido, fenoxi no sustituido o mono- o poli-sustituido, fenilacetilenilo no sustituido o mono- o poli-sustituido, piridiloxi no sustituido o mono- o poli-sustituido, o fenilsulfanilo no sustituido o mono- o poli-sustituido, en donde los sustituyentes en cada caso pueden ser independientes uno del otro y se seleccionan del grupo que consiste de R1 y halogeno; R9 es halogeno, nitro, ciano, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloalcoxi C3-6, cicloalquilamino C3-6, cicloalquiltio C3-6, alqueniloxi C2-6, haloalqueniloxi C2-6, alquiltio C1-6, haloalquiltio C1-6, alquilsulfoniloxi C1-6, haloalquilsulfoniloxi C1-6, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, alqueniltio C2-6, haloalqueniltio C2-6, alquenilsulfinilo C2-6, haloalquenilsulfinilo C2-6, alquenilsulfonilo C2-6, haloalquenilsulfonilo C2-6, alquilamino C1-6, dialquilamino C1-6, alquilsulfonilamino C1-6, haloalquilsulfonilamino C1-6, alquilcarbonilo C1-6, haloalquilcarbonilo C1-6, alcoxicarbonilo C1-6, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, fenilamino no sustituido o mono- o poli-sustituido, arilsulfonilo no sustituido o mono- o poli-sustituido, fenilcarbonilo no sustituido o mono- o poli-sustituido, fenilmetoximino no sustituido o mono- o poli-sustituido, fenilhidroximetilo no sustituido o mono- o poli-sustituido, 1-p-fenil-1-hidroxietilo no sustituido o mono- o poli-sustituido, fenilclorometilo no sustituido o mono- o poli- sustituido, fenilcianometilo no sustituido o mono- o poli-sustituido, fenilo no sustituido o mono- o poli-sustituido, fenoxi no sustituido o mono- o poli-sustituido, fenilacetilenilo no sustituido o mono- o poli-sustituido, fenoxi no sustituido o mono- o poli-sustituido, o piridiloxi, en donde los sustituyentes en cada caso pueden ser independientes uno del otro y se seleccionan del grupo que consiste de R1 y halogeno; a es 1, 2, 3 o 4; b es 0, 1, 2, 3 o 4; m, n, o y p son, independientemente uno del otro, 0, 1, 2, 3, 4 o 5; W es O, S, S(O2), N(R1), alquilo C1-6 o haloalquilo C1-6; Y es O, S o N(R11); y R11 es alquilo C1-6 o fenilo no sustituido o mono- o poli-sustituido; siempre que m y p no sean iguales a 0 al mismo tiempo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04013690 | 2004-06-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR049391A1 true AR049391A1 (es) | 2006-07-26 |
Family
ID=34925324
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050102344A AR049391A1 (es) | 2004-06-10 | 2005-06-08 | Derivados de aminoacetonitrilo y su uso para controlar parasitos en animales de sangre caliente |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7642379B2 (es) |
| EP (1) | EP1758849A1 (es) |
| JP (1) | JP2008501761A (es) |
| AR (1) | AR049391A1 (es) |
| AU (1) | AU2005251917B2 (es) |
| TW (1) | TW200613251A (es) |
| WO (1) | WO2005121075A1 (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0402677D0 (en) * | 2003-11-06 | 2004-03-10 | Novartis Ag | Organic compounds |
| WO2008062005A1 (en) * | 2006-11-24 | 2008-05-29 | Novartis Ag | The use of aminoacetonitril compounds in the control of endoparasites in warm- blood animals. |
| NZ578259A (en) | 2007-02-09 | 2011-12-22 | Pfizer Ltd | Antiparasitic agents |
| JP5327876B2 (ja) | 2007-02-21 | 2013-10-30 | ゾエティス・ユーケイ・リミテッド | ベンゾフラン抗寄生虫剤 |
| EP2155699B9 (en) | 2007-05-15 | 2016-09-14 | Merial, Inc. | Aryloazol-2-yl cyanoethylamino compounds, method of making and method of using thereof |
| EA026649B1 (ru) | 2008-10-21 | 2017-05-31 | Мериал, Инк. | Тиоамидные соединения, способ их получения и способ их применения |
| MX2011005011A (es) | 2008-11-14 | 2011-07-29 | Merial Ltd | Compuestos de arilazol-2-il-cianoetilamino enantiomericamente enriquecidos, metodo de elaboracion y de uso de los mismos. |
| WO2013138863A1 (en) * | 2012-03-23 | 2013-09-26 | Newsouth Innovations Pty Limited | Kinase inhibitors for the treatment of cancer |
| US8822689B2 (en) | 2012-09-19 | 2014-09-02 | Merial Limited | Aryloazol-2-yl cyanoethylamino compounds, method of making and method of using thereof |
| AR094961A1 (es) | 2013-03-15 | 2015-09-09 | Lilly Co Eli | 1-hidroxi-benzooxaboroles como agentes antiparasitarios |
| WO2020112374A1 (en) | 2018-11-20 | 2020-06-04 | Boehringer Ingelheim Animal Health USA Inc. | Indazolylcyanoethylamino compound, compositions of same, method of making, and methods of using thereof |
| WO2021177334A1 (ja) * | 2020-03-04 | 2021-09-10 | 国立大学法人山口大学 | 新規なフルオロアルカン誘導体及びそれらを用いたゲル化剤 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3457294A (en) | 1966-04-22 | 1969-07-22 | Abbott Lab | N-(substituted-benzoyl) aminoaceto- and aminopropionitriles |
| GB8530015D0 (en) | 1985-12-05 | 1986-01-15 | Ici Plc | Biologically active amide derivatives |
| US6239077B1 (en) | 1998-05-01 | 2001-05-29 | Nihon Nohyaku Co., Ltd. | Aminoacetonitrile derivative agricultural and horticultural insecticide containing the same and use thereof |
| KR100850252B1 (ko) * | 2000-12-20 | 2008-08-04 | 노파르티스 아게 | 유기 화합물 |
| AR035531A1 (es) * | 2001-01-22 | 2004-06-02 | Novartis Ag | Composicion para el control de plagas endoparasiticas en ganados y animales domesticos, un metodo para su control y el uso de dicha composicion para la preparacion de medicamentos |
| WO2003004474A1 (en) * | 2001-07-06 | 2003-01-16 | Syngenta Participations Ag | Pesticidally active aminoacetonitriles |
| TW200305556A (en) * | 2002-03-21 | 2003-11-01 | Novartis Ag | Organic compounds |
| AR040229A1 (es) * | 2002-05-22 | 2005-03-23 | Novartis Ag | Amidoacetonitrilos |
| TW200400932A (en) | 2002-06-19 | 2004-01-16 | Novartis Ag | Organic compounds |
-
2005
- 2005-06-08 TW TW094118870A patent/TW200613251A/zh unknown
- 2005-06-08 AR ARP050102344A patent/AR049391A1/es unknown
- 2005-06-09 JP JP2007526305A patent/JP2008501761A/ja active Pending
- 2005-06-09 US US11/596,961 patent/US7642379B2/en not_active Expired - Fee Related
- 2005-06-09 WO PCT/EP2005/006207 patent/WO2005121075A1/en not_active Application Discontinuation
- 2005-06-09 AU AU2005251917A patent/AU2005251917B2/en not_active Ceased
- 2005-06-09 EP EP05751761A patent/EP1758849A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| JP2008501761A (ja) | 2008-01-24 |
| US20080194693A1 (en) | 2008-08-14 |
| TW200613251A (en) | 2006-05-01 |
| EP1758849A1 (en) | 2007-03-07 |
| US7642379B2 (en) | 2010-01-05 |
| AU2005251917A1 (en) | 2005-12-22 |
| AU2005251917B2 (en) | 2009-02-12 |
| WO2005121075A1 (en) | 2005-12-22 |
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