AR099120A1 - DERIVATIVES OF QUINOLINE AS INSECTICIDES AND ACARICIDES - Google Patents
DERIVATIVES OF QUINOLINE AS INSECTICIDES AND ACARICIDESInfo
- Publication number
- AR099120A1 AR099120A1 ARP150100125A ARP150100125A AR099120A1 AR 099120 A1 AR099120 A1 AR 099120A1 AR P150100125 A ARP150100125 A AR P150100125A AR P150100125 A ARP150100125 A AR P150100125A AR 099120 A1 AR099120 A1 AR 099120A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- halogen
- cyano
- nitro
- Prior art date
Links
- 239000000642 acaricide Substances 0.000 title abstract 2
- 239000002917 insecticide Substances 0.000 title abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical class N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 title 1
- 150000002367 halogens Chemical group 0.000 abstract 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 10
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- -1 cyano, hydroxy Chemical group 0.000 abstract 5
- 150000002431 hydrogen Chemical group 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 4
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 1
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl 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
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000003636 chemical group Chemical group 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 239000003574 free electron Substances 0.000 abstract 1
- 125000006809 haloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 239000011630 iodine Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical class C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La presente solicitud se refiere a compuestos, procedimiento para su preparación y su uso como insecticidas y acaricidas. Reivindicación 1: Compuestos de la formula general (1) en la que R¹ representa halógeno, nitro, ciano, representa alquilo C₁₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, alquilcarbonilo C₁₋₆, alcoxicarbonilo C₁₋₆, alcoxiimino C₁₋₆-alquilo C₁₋₆ o alquilsulfoniloxi C₁₋₆ dado el caso mono- o polisustituidos con halógeno, o R¹ representa una cadena de carbono C₁₋₄ que dado el caso contiene 1 ó 2 heteroátomos, que está unida en dos posiciones de anillo adyacentes y forma un anillo alifático, aromático, heteroaromático o heterocíclico el cual, dado el caso está mono- o polisustituido con alquilo C₁₋₆ o con halógeno, siendo entonces n igual a 1 y siendo los heteroátomos seleccionados del grupo que se compone de N, S y O; n representa 1, 2, 3, 4 ó 5; R² representa hidrógeno, halógeno, ciano, hidroxi o representa alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆ o alcoxi C₁₋₆ dado el caso mono- o polisustituidos, de manera igual o diferente, habiéndose seleccionado los sustituyentes independientemente entre sí de flúor, cloro, bromo o yodo; R³ representa hidrógeno, representa alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₃₋₄, alquilcarbonilo C₁₋₄ o alcoxicarbonilo C₁₋₄ dado el caso mono- o polisustituidos, de manera igual o diferente, habiéndose seleccionado los sustituyentes independientemente entre sí de ciano, halógeno, alquilo C₁₋₄ o alcoxi C₁₋₄; Q¹ representa C-R⁴ o N; Q² representa C-R⁴; Q³ representa C-R⁴; Q⁴ representa C-R⁴ o N; siendo que Q¹ representa C-R⁴, cuando Q⁴ representa N y Q⁴ representa C-R⁴, cuando Q¹ representa N; R⁴ representa hidrógeno, halógeno, nitro, ciano, alquilo C₁₋₄, haloalquilo C₁₋₄ o alcoxi C₁₋₄; R⁶ representa hidrógeno, halógeno, nitro, ciano, representa alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆, alcoxi C₁₋₆, (alcoxi C₁₋₆)carbonilo, alquilamino C₁₋₆, formilo, (alquil-C₁₋₆)carbonilo, alcoxiimino C₁₋₆-alquilo C₁₋₆, dialquilamino C₁₋₆, (alquilamino C₁₋₆)carbonilo, (dialquilamino C₁₋₆)carbonilo, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, alquilaminosulfonilo C₁₋₆ o alquilsulfonilamino C₁₋₆ dado el caso mono- o polisustituidos, de manera igual o diferente, habiéndose seleccionado los sustituyentes independientemente entre sí de halógeno, ciano, nitro, hidroxi, amino, alquilo C₁₋₆, alcoxi C₁₋₆, cicloalquilo C₃₋₆, haloalcoxi C₁₋₆ o alquiltio C₁₋₆; X representa haloalquilo C₁₋₆ que dado el caso puede estar mono- a trisustituido adicionalmente, habiéndose seleccionado los sustituyentes independientemente entre sí de hidroxi, ciano o alcoxi C₁₋₄; W representa O ó S; G representa un par de electrones libre o representa oxígeno; A representa un grupo químico bivalente, que está seleccionado de los grupos -C(=O)NR¹³-, -C(=S)NR¹³-, -C(=O)NR¹³-NR¹⁶-, -C(=O)NR¹³C(R¹⁴)(R¹⁵)C(=O)NR¹⁶-, C(R¹⁴)(R¹⁵)NR¹³-C(=O)-, -CH=N-N(R¹³)-C(=W)-N(R¹⁶)-, -N(R¹³)-N(R¹⁶)-C(=O)- en el que el punto de unión (izquierdo) mencionado en cada caso en primer lugar se enlaza en el anillo y el punto de unión (derecho) mencionado en cada caso en segundo lugar se enlaza con Y; R¹³, R¹⁶ independientemente entre sí representan hidrógeno, representan alquilo C₁₋₄, alcoxi C₁₋₄-alquilo C₁₋₄, cianoalquilo C₁₋₄, cicloalquilo C₃₋₆, alquilcarbonilo C₁₋₄, alcoxicarbonilo C₁₋₄ o alquenilo C₂₋₄; R¹⁴, R¹⁵ independientemente entre sí representan hidrógeno o representan alquilo C₁₋₄ o R¹⁴, R¹⁵ juntos forman un anillo alifático de 3 a 6 miembros; Y representa hidrógeno o representa alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆ o cicloalquenilo C₃₋₆ dado el caso mono- o polisustituidos, de manera igual o diferente, habiéndose seleccionado los sustituyentes de halógeno, nitro, ciano, hidroxi, aminotiocarbonilo, aminocarbonilo, alquilaminocarbonilo C₁₋₄, alquilaminotiocarbonilo C₁₋₄, haloalquilaminocarbonilo C₁₋₄, di-(alquil-C₁₋₄)-aminocarbonilo, di-(alquil-C₁₋₄)-aminotiocarbonilo, hidroxicarbonilo, alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₆, alquil C₁₋₄-cicloalquilo C₃₋₄, alquenilo C₂₋₆, alquinilo C₂₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, alcoxicarbonilo C₁₋₆, alquilcarbonilo C₁₋₆, alcoxiimino C₁₋₄-alquilo C₁₋₄, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆,alquilsulfonilo C₁₋₆ o de arilo o heteroarilo dado el caso mono- o polisustituidos, de manera igual o diferente, habiéndose seleccionado los sustituyentes de halógeno, nitro, ciano, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₆ o haloalcoxi C₁₋₆, o Y representa heterociclilo, arilo, aril-alquilo C₁₋₄, hetarilo, oxo-heterociclilo o hetaril-alquilo C₁₋₄ dado el caso sustituidos, habiéndose seleccionado los sustituyentes de halógeno, nitro, ciano, hidroxi, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₆, o haloalcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆ o alquilsulfonilo C₁₋₆; así como sales y N-óxidos de compuestos de la fórmula (1). Reivindicación 10: Ácidos quinolincarboxílicos de la fórmula (2) en la que R⁴ᵃ, R⁴ᵇ, R⁴ᶜ y R⁴ᵈ independientemente entre sí tienen el significado descrito para R⁴ en la reivindicación 4 y R⁶ tiene el significado indicado en la reivindicación 4.The present application refers to compounds, process for their preparation and their use as insecticides and acaricides. Claim 1: Compounds of the general formula (1) wherein R¹ represents halogen, nitro, cyano, represents C₁₋₆ alkyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl, C₁ alkylsulfonyl ₋₆, C₁₋₆ alkylcarbonyl, C₁₋₆ alkoxycarbonyl, C₁₋₆ alkoxyimino-C₁₋₆ alkyl or Cils-alkylsulfonyloxy, where appropriate mono- or polysubstituted with halogen, or R¹ represents a C₁₋₄ carbon chain given the case contains 1 or 2 heteroatoms, which is attached in two adjacent ring positions and forms an aliphatic, aromatic, heteroaromatic or heterocyclic ring which, if necessary, is mono- or polysubstituted with C₁₋₆ alkyl or halogen, then being n equal to 1 and the heteroatoms being selected from the group consisting of N, S and O; n represents 1, 2, 3, 4 or 5; R² represents hydrogen, halogen, cyano, hydroxy or represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl or C₁₋₆ alkoxy, if the case is mono- or polysubstituted, in the same or different manner, the substituents having been independently selected from yes of fluorine, chlorine, bromine or iodine; R³ represents hydrogen, represents C₁₋₄ alkyl, C₂₋₄ alkenyl, C₃₋₄ alkynyl, C₁₋₄ alkylcarbonyl or C₁₋₄ alkoxycarbonyl, if the case is mono- or polysubstituted, in the same or different manner, the substituents having been independently selected from each other cyano, halogen, C₁₋₄ alkyl or C₁₋₄ alkoxy; Q¹ represents C-R⁴ or N; Q² represents C-R⁴; Q³ represents C-R⁴; Q⁴ represents C-R⁴ or N; being that Q¹ represents C-R⁴, when Q⁴ represents N and Q⁴ represents C-R⁴, when Q¹ represents N; R⁴ represents hydrogen, halogen, nitro, cyano, C₁₋₄ alkyl, C₁₋₄ haloalkyl or C₁₋₄ alkoxy; R⁶ represents hydrogen, halogen, nitro, cyano, represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, (C₁₋₆ alkoxy) carbonyl, C₁₋₆ alkylamino, formyl , (C-alkyl) carbonyl, C₁₋₆ alkoxyimino-C₁₋₆ alkyl, Cquila dialkylamino, (C₁₋₆ alkylamino) carbonyl, (C₁₋₆ dialkylamino) carbonyl, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl , C₁₋₆ alkylsulfonyl, C₁₋₆ alkylaminosulfonyl or C₁₋₆ alkylsulfonylamino, in the same or different manner, the substituents having been independently selected from each other from halogen, cyano, nitro, hydroxy, amino, C₁₋ alkyl ₆, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₁₋₆ haloalkoxy or C₁₋₆ alkylthio; X represents C₁₋₆ haloalkyl which, if necessary, may be additionally mono-substituted, the substituents having been independently selected from each other of hydroxy, cyano or C₁₋₄ alkoxy; W represents O or S; G represents a free electron pair or represents oxygen; A represents a bivalent chemical group, which is selected from the groups -C (= O) NR¹³-, -C (= S) NR¹³-, -C (= O) NR¹³-NR¹⁶-, -C (= O) NR¹³C ( R¹⁴) (R¹⁵) C (= O) NR¹⁶-, C (R¹⁴) (R¹⁵) NR¹³-C (= O) -, -CH = NN (R¹³) -C (= W) -N (R¹⁶) -, - N (R¹³) -N (R¹⁶) -C (= O) - where the junction point (left) mentioned in each case is first linked to the ring and the junction point (right) mentioned in each case secondly it is linked with Y; R¹³, R¹⁶ independently represent each other hydrogen, represent C₁₋₄ alkyl, C₁₋₄ alkoxy-C₁₋₄ alkyl, Ciano cyanoalkyl, C₃₋₆ cycloalkyl, C₁₋₄ alkylcarbonyl, C₁₋₄ alkoxycarbonyl or C₂₋₄ alkenyl; R¹⁴, R¹⁵ independently of each other represent hydrogen or represent C₁₋₄ or R¹⁴ alkyl, R¹⁵ together form a 3- to 6-membered aliphatic ring; Y represents hydrogen or represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₆ cycloalkyl or C₃₋₆ cycloalkenyl, in the same or different case, in the same or different manner, the halogen substituents having been selected, nitro, cyano, hydroxy, aminothiocarbonyl, aminocarbonyl, C₁₋₄ alkylaminocarbonyl, C₁₋₄ alkylaminothiocarbonyl, C₁₋₄ haloalkylaminocarbonyl, di- (C--alkyl) -aminocarbonyl, di- (C-alkyl) -amino-thiocarbonyl, hydroxycarbonyl , C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₃₋₆ cycloalkyl, C₁₋₄ alkyl-C₃₋₄ cycloalkyl, C₂₋₆ alkenyl, C₁₋₆ alkynyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₁₋₆ alkoxycarbonyl , C₁₋₆ alkylcarbonyl, C₁₋₄ alkoxyimino-C₁₋₄ alkyl, Cilt alkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ alkylsulfonyl or aryl or heteroaryl, where appropriate mono- or polysubstituted, equally or differently nte, the halogen, nitro, cyano, hydroxy, C₁₋₄ alkyl, C halo haloalkyl, C₁₋₆ alkoxy or C₁₋₆ haloalkoxy substituents having been selected, and Y represents heterocyclyl, aryl, aryl-C₁₋₄ alkyl, heteroaryl , substituted oxo-heterocyclyl or C-alkyl, where the halogen, nitro, cyano, hydroxy, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₆ alkoxy, or C₁₋₆ haloalkoxy substituents have been selected, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl or C₁₋₆ alkylsulfonyl; as well as salts and N-oxides of compounds of the formula (1). Claim 10: Quinolinecarboxylic acids of the formula (2) in which R⁴ᵃ, R⁴ᵇ, R⁴ᶜ and R⁴ᵈ independently of one another have the meaning described for R⁴ in claim 4 and R⁶ has the meaning indicated in claim 4.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14151727 | 2014-01-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR099120A1 true AR099120A1 (en) | 2016-06-29 |
Family
ID=49949588
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150100125A AR099120A1 (en) | 2014-01-20 | 2015-01-16 | DERIVATIVES OF QUINOLINE AS INSECTICIDES AND ACARICIDES |
Country Status (4)
| Country | Link |
|---|---|
| AR (1) | AR099120A1 (en) |
| TW (1) | TW201612161A (en) |
| UY (1) | UY35958A (en) |
| WO (1) | WO2015107133A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR099336A1 (en) | 2014-02-17 | 2016-07-13 | Bayer Cropscience Ag | INDOL- AND BENCIMIDAZOLCARBOXAMIDS AS INSECTICIDES AND ACARICIDES |
| CA3054540A1 (en) * | 2017-03-17 | 2018-09-20 | Meiji Seika Pharma Co., Ltd. | Mesostigmata mite control agent |
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| DE19638486A1 (en) | 1996-09-20 | 1998-03-26 | Basf Ag | Hetaroyl derivatives |
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| TWI430995B (en) | 2007-06-26 | 2014-03-21 | Du Pont | Naphthalene isoxazoline invertebrate pest control agents |
| GB0720126D0 (en) | 2007-10-15 | 2007-11-28 | Syngenta Participations Ag | Chemical compounds |
| TWI411395B (en) | 2007-12-24 | 2013-10-11 | Syngenta Participations Ag | Insecticidal compounds |
| TWI401023B (en) | 2008-02-06 | 2013-07-11 | Du Pont | Mesoionic pesticides |
| JP2011530511A (en) | 2008-08-05 | 2011-12-22 | メルク・シャープ・エンド・ドーム・コーポレイション | Therapeutic compounds |
| CN101337940B (en) | 2008-08-12 | 2012-05-02 | 国家农药创制工程技术研究中心 | Nitrogen heterocyclic ring dichloro allyl ether compound with insecticidal activity |
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| WO2010069502A2 (en) | 2008-12-18 | 2010-06-24 | Bayer Cropscience Ag | Tetrazole substituted anthranilic acid amides as pesticides |
| CN101747320B (en) | 2008-12-19 | 2013-10-16 | 华东理工大学 | Dialdehyde-constructed nitrogen- or oxygen-containing heterocyclic compound with insecticidal activity and preparation method thereof |
| WO2010101949A1 (en) | 2009-03-02 | 2010-09-10 | Sirtris Pharmaceuticals, Inc. | 8-substituted quinolines and related analogs as sirtuin modulators |
| TWI482771B (en) | 2009-05-04 | 2015-05-01 | Du Pont | Nematocidal sulfonamides |
| JP2011042643A (en) | 2009-07-24 | 2011-03-03 | Bayer Cropscience Ag | Insecticidal carboxamides |
| UY32940A (en) | 2009-10-27 | 2011-05-31 | Bayer Cropscience Ag | AMIDAS REPLACED WITH HALOGENO RENT AS INSECTICIDES AND ACARICIDES |
| EP2789237A1 (en) | 2010-08-31 | 2014-10-15 | Meiji Seika Pharma Co., Ltd. | Pest control agent |
| CN101935291B (en) | 2010-09-13 | 2013-05-01 | 中化蓝天集团有限公司 | Cyano phthalic diamide compounds, preparation method thereof and use thereof as agricultural chemical pesticide |
| CN102057925B (en) | 2011-01-21 | 2013-04-10 | 陕西上格之路生物科学有限公司 | Insecticidal composition containing thiacloprid amide and biogenic insecticide |
| AR085509A1 (en) | 2011-03-09 | 2013-10-09 | Bayer Cropscience Ag | INDOL- AND BENCIMIDAZOLCARBOXAMIDS AS INSECTICIDES AND ACARICIDES |
| AU2012273007A1 (en) | 2011-06-23 | 2014-01-30 | Viamet Pharmaceuticals (NC), Inc. | Metalloenzyme inhibitor compounds |
-
2015
- 2015-01-16 WO PCT/EP2015/050732 patent/WO2015107133A1/en not_active Ceased
- 2015-01-16 TW TW104101413A patent/TW201612161A/en unknown
- 2015-01-16 AR ARP150100125A patent/AR099120A1/en unknown
- 2015-01-19 UY UY0001035958A patent/UY35958A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| TW201612161A (en) | 2016-04-01 |
| WO2015107133A1 (en) | 2015-07-23 |
| UY35958A (en) | 2015-08-31 |
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