AR109677A1 - Derivados heterocíclicos bicíclicos fusionados como plaguicidas - Google Patents
Derivados heterocíclicos bicíclicos fusionados como plaguicidasInfo
- Publication number
- AR109677A1 AR109677A1 ARP170102587A ARP170102587A AR109677A1 AR 109677 A1 AR109677 A1 AR 109677A1 AR P170102587 A ARP170102587 A AR P170102587A AR P170102587 A ARP170102587 A AR P170102587A AR 109677 A1 AR109677 A1 AR 109677A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- alkylsulfinyl
- alkylthio
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 54
- -1 C2−6 cyanoalkenyl Chemical group 0.000 abstract 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 8
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 7
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 7
- 125000001072 heteroaryl group Chemical group 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 6
- 125000005089 alkenylaminocarbonyl group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 5
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 5
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 5
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 5
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 5
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 5
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 4
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 4
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 4
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 abstract 3
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 3
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 3
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 3
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 3
- 125000005103 alkyl silyl group Chemical group 0.000 abstract 3
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 3
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 3
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 3
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 3
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 239000000642 acaricide Substances 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- GGWBHVILAJZWKJ-KJEVSKRMSA-N ranitidine hydrochloride Chemical compound [H+].[Cl-].[O-][N+](=O)\C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 GGWBHVILAJZWKJ-KJEVSKRMSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/02—Acaricides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
- A01P7/04—Insecticides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Insects & Arthropods (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
La presente solicitud se refiere a compuestos, su aplicación como acaricidas y/o insecticidas para combatir plagas de animales y procesos e intermediarios para su preparación. Reivindicación 1: Compuestos de la fórmula (1), en donde Aa representa nitrógeno o =C(R¹⁰)-, Ab representa nitrógeno o =C(R¹¹)-, Ac representa nitrógeno o =C(R¹²)-, Ad representa nitrógeno o =C(R¹³)-, donde Aa, Ab, Ac y Ad pueden representar como máximo dos nitrógenos; R¹ representa C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₁₋₆ haloalcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alqueniloxi-C₁₋₆ alquilo, C₂₋₆ haloalqueniloxi-C₁₋₆ alquilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ alquiniloxi-C₁₋₆ alquilo, C₂₋₆ haloalquiniloxi-C₁₋₆ alquilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquil-C₃₋₈ cicloalquilo, C₁₋₆ alquil-C₃₋₈ cicloalquilo, halo-C₃₋₈ cicloalquilo, amino, C₁₋₆ alquilamino, di-C₁₋₆ alquil-amino, C₃₋₈ cicloalquilamino, C₁₋₆ alquilcarbonilamino, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ haloalquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinil-C₁₋₆ alquilo, C₁₋₆ haloalquilsulfinil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonil-C₁₋₆ alquilo, C₁₋₆ haloalquilsulfonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonil-C₁₋₆ alquilo, C₁₋₆ alquilcarbonil-C₁₋₆ alquilo, C₁₋₆ haloalquilcarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ haloalcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilamino, aminosulfonil-C₁₋₆ alquilo, C₁₋₆ alquilaminosulfonil-C₁₋₆ alquilo, di-C₁₋₆ alquil-aminosulfonil-C₁₋₆ alquilo, o representa C₁₋₆ alquilo, C₁₋₆ alcoxi, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₃₋₈ cicloalquilo opcionalmente sustituido en cada caso una o más veces en forma igual o diferente con arilo, hetarilo o heterociclilo, donde arilo, hetarilo o heterociclilo puede estar opcionalmente sustituido en cada caso una o más veces en forma igual o diferente con halógeno, ciano, nitro, hidroxi, amino, carboxi, carbamoílo, aminosulfonilo, C₁₋₆ alquilo, C₃₋₆cicloalquilo, C₁₋₆ alcoxi, C₁₋₆ haloalquilo, C₁₋₆ haloalcoxi, C₁₋₆ alquiltio, C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfimino, C₁₋₆ alquilsulfimino-C₁₋₆ alquilo, C₁₋₆ alquilsulfimino-C₂₋₆ alquilcarbonilo, C₁₋₆ alquilsulfoximino, C₁₋₆ alquilsulfoximino-C₁₋₆ alquilo, C₁₋₆ alquilsulfoximino-C₂₋₆ alquilcarbonilo, C₁₋₆ alcoxicarbonilo, C₁₋₆ alquilcarbonilo, C₃₋₆ trialquil-sililo o bencilo, o R¹ representa opcionalmente en cada caso arilo, hetarilo o heterociclilo sustituido una o más veces en forma igual o diferente con halógeno, ciano, nitro, hidroxi, amino, carboxi, carbamoílo, C₁₋₆ alquilo, C₃₋₈ cicloalquilo, C₁₋₆ alcoxi, C₁₋₆ haloalquilo, C₁₋₆ haloalocoxi, C₁₋₆ alquiltio, C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfimino, C₁₋₆ alquilsulfimino-C₁₋₆ alquilo, C₁₋₆ alquilsulfimino-C₂₋₆ alquilcarbonilo, C₁₋₆ alquilsulfoximino, C₁₋₆ alquilsulfoximino-C₁₋₆ alquilo, C₁₋₆ alquilsulfoximino-C₂₋₆ alquilcarbonilo, C₁₋₆ alcoxicarbonilo, C₁₋₆ alquilcarbonilo, C₃₋₆ trialquilsililo, (=O) (sólo en el caso de heterociclilo) o (=O)₂ (sólo en el caso de heterociclilo); R¹⁰, R¹¹, R¹², R¹³ en forma independiente entre sí representan hidrógeno, ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsililo, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquil-C₃₋₈ cicloalquilo, C₁₋₆ alquil-C₃₋₈ cicloalquilo, halo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquil-C₁₋₆ alcoxiimino, C₁₋₆ haloalquil-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonil-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ alquiltiocarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquil-aminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₃₋₈ cicloalquilamino, NHCO-C₁₋₆ alquilo (C₁₋₆ alquilcarbonilamino), o representan arilo o hetarilo opcionalmente sustituido en cada caso una o más veces en forma igual o diferente, donde (en el caso de hetarilo) opcionalmente puede estar presente al menos un grupo carbonilo y/o donde los sustituyentes se seleccionan entre: ciano, carboxilo, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsililo, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquil-C₃₋₈ cicloalquilo, C₁₋₆ alquil-C₃₋₈ cicloalquilo, halo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquil-C₁₋₆ alcoxiimino, C₁₋₆ haloalquil-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonil-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquilaminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquilaminotiocarbonilo, C₃₋₈ cicloalquilamino, C₁₋₆ alquilcarbonilamino, donde sólo uno o dos de los residuos R¹⁰, R¹¹, R¹², R¹³ representan un sustituyente diferente de hidrógeno; Q representa un sistema de anillos bicíclico o tricíclico parcialmente saturado o saturado heterocíclico o heteroaromático de 8, 9, 10, 11 ó 12 miembros, donde opcionalmente puede estar presente al menos un grupo carbonilo y/o donde el sistema de anillos está opcionalmente sustituido una o más veces en forma igual o diferente, y los sustituyentes pueden seleccionarse en forma independiente entre si entre ciano, halógeno, nitro, acetilo, hidroxi, amino, SCN, tri-C₁₋₆ alquilsililo, C₃₋₈ cicloalquilo, C₃₋₈ cicloalquil-C₃₋₈ cicloalquilo, C₁₋₆ alquil-C₃₋₈ cicloalquilo, halo-C₃₋₈ cicloalquilo, C₁₋₆ alquilo, C₁₋₆ haloalquilo, C₁₋₆ cianoalquilo, C₁₋₆ hidroxialquilo, hidroxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alquilo, C₁₋₆ alcoxi-C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ haloalquenilo, C₂₋₆ cianoalquenilo, C₂₋₆ alquinilo, C₂₋₆ alquiniloxi-C₁₋₄alquilo, C₂₋₆ haloalquinilo, C₂₋₆ cianoalquinilo, C₁₋₆ alcoxi, C₁₋₆ haloalcoxi, C₁₋₆ haloalcoxi-C₁₋₆ alquilo, C₂₋₆ alqueniloxi-C₁₋₆ alquilo, C₂₋₆ haloalqueniloxi-C₁₋₆ alquilo, C₁₋₆ cianoalcoxi, C₁₋₆ alcoxicarbonil-C₁₋₆ alcoxi, C₁₋₆ alcoxi-C₁₋₆ alcoxi, C₁₋₆ alquilhidroxiimino, C₁₋₆ alcoxiimino, C₁₋₆ alquil-C₁₋₆ alcoxiimino, C₁₋₆ haloalquil-C₁₋₆ alcoxiimino, C₁₋₆ alquiltio, C₁₋₆ haloalquiltio, C₁₋₆ alcoxi-C₁₋₆ alquiltio, C₁₋₆ alquiltio-C₁₋₆ alquilo, C₁₋₆ alquilsulfinilo, C₁₋₆ haloalquilsulfinilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfinilo, C₁₋₆ alquilsulfinil-C₁₋₆ alquilo, C₁₋₆ alquilsulfonilo, C₁₋₆ haloalquilsulfonilo, C₁₋₆ alcoxi-C₁₋₆ alquilsulfonilo, C₁₋₆ alquilsulfonil-C₁₋₆ alquilo, C₁₋₆ alquilsulfoniloxi, C₁₋₆ alquilcarbonilo, C₁₋₆ alquilcarbonil-C₁₋₆ alquilo, C₁₋₆ alquiltiocarbonilo, C₁₋₆ haloalquilcarbonilo, C₁₋₆ alquilcarboniloxi, C₁₋₆ alcoxicarbonilo, C₁₋₆ haloalcoxicarbonilo, aminocarbonilo, C₁₋₆ alquilaminocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₂₋₆ alquenilaminocarbonilo, di-C₂₋₆ alquenilaminocarbonilo, C₃₋₈ cicloalquilaminocarbonilo, C₁₋₆ alquilsulfonilamino, C₁₋₆ alquilamino, di-C₁₋₆ alquilamino, aminosulfonilo, C₁₋₆ alquilaminosulfonilo, di-C₁₋₆ alquil-aminosulfonilo, C₁₋₆ alquilsulfoximino, aminotiocarbonilo, C₁₋₆ alquilaminotiocarbonilo, di-C₁₋₆ alquil-aminotiocarbonilo, C₃₋₈ cicloalquilamino, NHCO-C₁₋₆ alquilo (C₁₋₆ alquilcarbonilamino), o los sustituyentes pueden seleccionarse en forma independiente entre si entre fenilo o un anillo heteroaromático de 5 ó 6 miembros, donde fenilo o el anillo puede estar opcionalmente sustituido una o más veces, en forma igual o diferente con C₁₋₆ alquilo, C₂₋₆ alquenilo, C₂₋₆ alquinilo, C₃₋₆ cicloalquilo, C₁₋₆ haloalquilo, C₂₋₆ haloalquenilo, C₂₋₆ haloalquinilo, C₃₋₆ halocicloalquilo, halógeno, CN, NO₂, C₁₋₄ alcoxi, C₁₋₄ haloalcoxi; n representa 0, 1 ó 2.
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Family Cites Families (98)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2820062A (en) | 1954-08-11 | 1958-01-14 | Pure Oil Co | Preparation of organic thiols |
| US5374646A (en) | 1989-12-01 | 1994-12-20 | Glaxo Group Limited | Benzofuran derivatives |
| US5576335A (en) | 1994-02-01 | 1996-11-19 | Nisshin Flour Milling Co., Ltd. | Urea derivatives and their use as ACAT inhibitors |
| PA8535601A1 (es) | 2000-12-21 | 2002-11-28 | Pfizer | Derivados benzimidazol y piridilimidazol como ligandos para gabaa |
| GB0213715D0 (en) | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
| FR2844794B1 (fr) | 2002-09-25 | 2004-12-03 | Atofina | Procede catalytique de fabrication d'alkylmercaptans par addition d'hydrogene |
| FR2844726B1 (fr) | 2002-09-25 | 2004-12-03 | Atofina | Procede catalytique de fabricaton de mercaptans a partir de thioethers |
| TWI312272B (en) | 2003-05-12 | 2009-07-21 | Sumitomo Chemical Co | Pyrimidine compound and pests controlling composition containing the same |
| CA2551867C (en) | 2003-12-31 | 2010-08-17 | Schering-Plough Ltd. | Control of parasites in animals by the use of imidazo[1,2-b]pyridazine derivatives |
| ES2241496B1 (es) | 2004-04-15 | 2006-12-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de piridina. |
| GB0414438D0 (en) | 2004-06-28 | 2004-07-28 | Syngenta Participations Ag | Chemical compounds |
| CN101039922B (zh) | 2004-10-20 | 2011-04-13 | 组合化学工业株式会社 | 3-三唑基苯基硫醚衍生物及含其作为有效成分的杀虫·杀螨·杀线虫剂 |
| JP5111113B2 (ja) | 2004-12-13 | 2012-12-26 | サネシス ファーマシューティカルズ， インコーポレイテッド | Ｒａｆキナーゼ阻害剤として有用なピリドピリミジノン、ジヒドロピリミドピリミジノンおよびプテリジノン |
| JP4871290B2 (ja) | 2005-10-06 | 2012-02-08 | 日本曹達株式会社 | 架橋環状アミン化合物および有害生物防除剤 |
| CA2624500A1 (en) | 2005-10-06 | 2007-04-19 | Schering Corporation | Pyrazolopyrimidines as protein kinase inhibitors |
| WO2009029625A1 (en) | 2007-08-27 | 2009-03-05 | Kalypsys, Inc. | 4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors |
| CA2706946A1 (en) | 2007-11-28 | 2009-06-04 | Schering Corporation | 2-fluoropyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| RU2369600C1 (ru) * | 2008-01-24 | 2009-10-10 | Андрей Александрович Иващенко | ЗАМЕЩЕННЫЕ 4-СУЛЬФОНИЛ-ПИРАЗОЛЫ И 3-СУЛЬФОНИЛ-ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ5-HT6 РЕЦЕПТОРОВ, АКТИВНЫЙ КОМПОНЕНТ, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, ЛЕКАРСТВЕННОЕ СРЕДСТВО И СПОСОБЫ ИХ ПОЛУЧЕНИЯ |
| EP2248817B1 (en) * | 2008-01-24 | 2015-01-07 | Alla Chem, LLC. | Substituted 2-amino-3-sulfonyl-pyrazolo[1,5-a] pyrimidines/antagonists of serotonin 5-ht6 receptors, methods for the production and the use thereof |
| TW200944520A (en) | 2008-01-29 | 2009-11-01 | Glaxo Group Ltd | Spiro compounds as NPY Y5 receptor antagonists |
| JP5369854B2 (ja) | 2008-04-21 | 2013-12-18 | 住友化学株式会社 | 有害節足動物防除組成物および縮合複素環化合物 |
| RU2384581C2 (ru) * | 2008-05-07 | 2010-03-20 | Андрей Александрович Иващенко | ЗАМЕЩЕННЫЕ 2-АМИНО-3-СУЛЬФОНИЛ-ТЕТРАГИДРО-ПИРАЗОЛО[1,5-a]ПИРИДО-ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-HT6 РЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ |
| JP5268461B2 (ja) | 2008-07-14 | 2013-08-21 | Ｍｅｉｊｉ Ｓｅｉｋａファルマ株式会社 | Ｐｆ１３６４物質、その製造方法、生産菌株、及び、それを有効成分とする農園芸用殺虫剤 |
| CN101337940B (zh) | 2008-08-12 | 2012-05-02 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
| CN101337937B (zh) | 2008-08-12 | 2010-12-22 | 国家农药创制工程技术研究中心 | 具有杀虫活性的n-苯基-5-取代氨基吡唑类化合物 |
| CN102223798A (zh) | 2008-09-24 | 2011-10-19 | 巴斯夫欧洲公司 | 用于防治无脊椎动物害虫的吡唑化合物 |
| CN101715774A (zh) | 2008-10-09 | 2010-06-02 | 浙江化工科技集团有限公司 | 一个具有杀虫活性化合物制备及用途 |
| EP2184273A1 (de) | 2008-11-05 | 2010-05-12 | Bayer CropScience AG | Halogen-substituierte Verbindungen als Pestizide |
| GB0820344D0 (en) | 2008-11-06 | 2008-12-17 | Syngenta Ltd | Herbicidal compositions |
| JP2012517439A (ja) | 2009-02-06 | 2012-08-02 | エラン ファーマシューティカルズ，インコーポレイテッド | Ｊｕｎｎ−末端キナーゼの阻害薬 |
| WO2010125985A1 (en) | 2009-04-28 | 2010-11-04 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use thereof |
| TW201116532A (en) | 2009-08-05 | 2011-05-16 | Merz Pharma Gmbh & Co Kgaa | Metabotropic glutamate receptor modulators |
| GB0917090D0 (en) * | 2009-09-29 | 2009-11-11 | Ucl Biomedica Plc | T-cell receptor |
| WO2011040629A1 (en) | 2009-09-30 | 2011-04-07 | Sumitomo Chemical Company, Limited | Composition and method for controlling arthropod pests |
| JP5540640B2 (ja) | 2009-10-07 | 2014-07-02 | 住友化学株式会社 | 複素環化合物及びその有害節足動物防除用途 |
| WO2011050284A1 (en) | 2009-10-23 | 2011-04-28 | Glaxosmithkline Llc | Pyrazolylpyridine antiviral agents |
| JP5543980B2 (ja) | 2009-12-18 | 2014-07-09 | 田辺三菱製薬株式会社 | 新規抗血小板薬 |
| WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
| WO2011085575A1 (zh) | 2010-01-15 | 2011-07-21 | 江苏省农药研究所股份有限公司 | 邻杂环甲酰苯胺类化合物及其合成方法和应用 |
| EP2959775A1 (en) | 2010-08-31 | 2015-12-30 | Meiji Seika Pharma Co., Ltd. | Pest control agent |
| CN101967139B (zh) | 2010-09-14 | 2013-06-05 | 中化蓝天集团有限公司 | 一种含一氟甲氧基吡唑的邻甲酰氨基苯甲酰胺类化合物、其合成方法及应用 |
| WO2012067822A1 (en) | 2010-11-16 | 2012-05-24 | Abbott Laboratories | Pyrazolo [1, 5 -a] pyrimidin potassium channel modulators |
| JP2013542966A (ja) | 2010-11-19 | 2013-11-28 | エフ．ホフマン−ラ ロシュ アーゲー | ピラゾロピリジンならびにｔｙｋ２阻害剤としてのピラゾロピリジン及びそれらの使用 |
| TW201242962A (en) | 2010-12-01 | 2012-11-01 | Sumitomo Chemical Co | Pyrimidine compound and use for pest control thereof |
| TWI617559B (zh) | 2010-12-22 | 2018-03-11 | 江蘇恆瑞醫藥股份有限公司 | ２－芳基咪唑并［１，２－ｂ］嗒．２－苯基咪唑并［１，２－ａ］吡啶，和２－苯基咪唑并［１，２－ａ］吡衍生物 |
| PH12013501178A1 (en) | 2010-12-24 | 2013-07-15 | Sumitomo Chemical Co | Fused heterocyclic compound and use for pest control thereof |
| JP5931752B2 (ja) | 2011-02-01 | 2016-06-08 | 協和発酵キリン株式会社 | 縮環複素環誘導体 |
| US20120302573A1 (en) | 2011-05-25 | 2012-11-29 | Paul Francis Jackson | Methods of inhibiting pro matrix metalloproteinase activation |
| GB201109763D0 (en) | 2011-06-10 | 2011-07-27 | Ucl Business Plc | Compounds |
| US8975276B2 (en) | 2011-06-29 | 2015-03-10 | Bristol-Myers Squibb Company | Inhibitors of PDE10 |
| TWI545119B (zh) | 2011-08-04 | 2016-08-11 | 住友化學股份有限公司 | 稠合雜環化合物及其在病蟲害防制上之用途 |
| US9351973B2 (en) | 2011-09-22 | 2016-05-31 | Merck Sharp & Dohme Corp. | Pyrazolopyridyl compounds as aldosterone synthase inhibitors |
| WO2013050317A1 (en) | 2011-10-03 | 2013-04-11 | Syngenta Limited | Polymorphs of an isoxazoline derivative |
| CN102391261A (zh) | 2011-10-14 | 2012-03-28 | 上海交通大学 | 一种n-取代噁二嗪类化合物及其制备方法和应用 |
| ES2661444T3 (es) | 2011-12-28 | 2018-04-02 | Fujifilm Corporation | Nuevo derivado de nicotinamida o sal del mismo |
| US9334238B2 (en) | 2012-03-30 | 2016-05-10 | Basf Se | N-substituted pyridinylidenes for combating animal pests |
| EP2647626A1 (en) | 2012-04-03 | 2013-10-09 | Syngenta Participations AG. | 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides |
| US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| MX2014013069A (es) | 2012-04-27 | 2015-07-06 | Dow Agrosciences Llc | Composiciones plaguicidas y procesos relacionados. |
| US9271500B2 (en) | 2012-06-18 | 2016-03-01 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound |
| WO2014014874A1 (en) | 2012-07-17 | 2014-01-23 | Boehringer Ingelheim International Gmbh | Pyrazole derivatives which inhibit leukotriene production |
| CN103232431B (zh) | 2013-01-25 | 2014-11-05 | 青岛科技大学 | 一种二卤代吡唑酰胺类化合物及其应用 |
| CN103109816B (zh) | 2013-01-25 | 2014-09-10 | 青岛科技大学 | 硫代苯甲酰胺类化合物及其应用 |
| WO2014158644A1 (en) | 2013-03-13 | 2014-10-02 | Dow Agrosciences Llc | Process for the preparation of triaryl rhamnose carbamates |
| UY35421A (es) | 2013-03-15 | 2014-10-31 | Nihon Nohyaku Co Ltd | Compuesto heterocíclico condensado o su sal, insecticida agrícola u hortícola que comprende el comp uesto y método de uso del insecticida |
| WO2014148451A1 (ja) | 2013-03-19 | 2014-09-25 | 日本農薬株式会社 | 縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| CA2907605A1 (en) | 2013-05-23 | 2014-11-27 | F. Hoffmann-La Roche Ag | 2-phenylimidazo[1,2-a]pyrimidines as imaging agents |
| US10939682B2 (en) | 2013-07-02 | 2021-03-09 | Syngenta Participations Ag | Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents |
| CN103524422B (zh) | 2013-10-11 | 2015-05-27 | 中国农业科学院植物保护研究所 | 苯并咪唑衍生物及其制备方法和用途 |
| MX2016004942A (es) | 2013-10-17 | 2016-06-28 | Dow Agrosciences Llc | Procesos para la preparacion de compuestos plaguicidas. |
| CN105636440A (zh) | 2013-10-17 | 2016-06-01 | 美国陶氏益农公司 | 制备杀虫化合物的方法 |
| EP2873668A1 (en) | 2013-11-13 | 2015-05-20 | Syngenta Participations AG. | Pesticidally active bicyclic heterocycles with sulphur containing substituents |
| WO2015121136A1 (de) | 2014-02-17 | 2015-08-20 | Bayer Cropscience Ag | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| CN106661022B (zh) * | 2014-05-08 | 2018-05-04 | 拜耳作物科学股份公司 | 作为杀线虫剂的吡唑并吡啶磺酰胺 |
| US10131669B2 (en) | 2014-07-24 | 2018-11-20 | Pfizer Inc. | Pyrazolopyrimidine compounds |
| JP6299534B2 (ja) * | 2014-09-03 | 2018-03-28 | 株式会社島津製作所 | 半導体レーザ励起固体レーザ装置及びレーザ光の出力方法 |
| CN107207495A (zh) * | 2014-12-02 | 2017-09-26 | 拜耳作物科学股份公司 | 作为害虫防治剂的双环化合物 |
| WO2016087417A1 (de) * | 2014-12-02 | 2016-06-09 | Bayer Cropscience Aktiengesellschaft | Bicyclische verbindungen als schädlingsbekämpfungsmittel |
| CN107406443A (zh) * | 2014-12-02 | 2017-11-28 | 拜耳作物科学股份公司 | 作为有害生物防治剂的双环化合物 |
| US20170265474A1 (en) * | 2014-12-02 | 2017-09-21 | Bayer Cropscience Aktiengesellschaft | Bicyclic compounds as pest control agents |
| JP2017537916A (ja) * | 2014-12-02 | 2017-12-21 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 有害生物防除剤としての二環式化合物 |
| US10308650B2 (en) | 2014-12-11 | 2019-06-04 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulfur containing substituents |
| BR112017014061B1 (pt) | 2014-12-29 | 2021-07-20 | Syngenta Participations Ag | Composto da formula i, composição pesticida, método para controle de pragas e método para a proteção de material de propagação de plantas a partir do mesmo |
| UY36548A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
| UY36547A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
| PT3257853T (pt) | 2015-02-12 | 2021-12-23 | Nissan Chemical Corp | Composto heterocíclico condensado e agente de controlo de organismos prejudiciais |
| US10188108B2 (en) | 2015-04-08 | 2019-01-29 | Bayer Cropscience Aktiengesellschaft | Fused bicyclic heterocycle derivatives as pesticides |
| JP2016199515A (ja) * | 2015-04-13 | 2016-12-01 | キユーピー株式会社 | 乳化化粧料 |
| WO2017061497A1 (ja) * | 2015-10-06 | 2017-04-13 | 日本農薬株式会社 | 縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| WO2017093180A1 (de) | 2015-12-01 | 2017-06-08 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2017125340A1 (de) | 2016-01-22 | 2017-07-27 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2017144341A1 (de) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| CA3016398A1 (en) * | 2016-03-10 | 2017-09-14 | Nissan Chemical Corporation | Condensed heterocyclic compounds and pesticides |
| EP3241830A1 (de) | 2016-05-04 | 2017-11-08 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| BR112019001135B1 (pt) * | 2016-07-19 | 2022-11-01 | Bayer Cropscience Aktiengesellschaft | Derivados de heterociclo bicíclico fundido como pesticidas, seu uso, formulação agroquímica, e método para controlar pragas animais |
| MA45918A (fr) | 2016-08-15 | 2019-06-19 | Bayer Ag | Dérivés hétérocycliques bicycliques condensés utilisés comme pesticides |
| KR20190084310A (ko) * | 2016-11-23 | 2019-07-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 살충제로서의 2-[3-(알킬술포닐)-2H-인다졸-2-일]-3H-이미다조[4,5-b]피리딘 유도체 및 유사한 화합물 |
| EP3305786A3 (de) | 2018-01-22 | 2018-07-25 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
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- 2017-09-15 US US16/333,385 patent/US10611779B2/en active Active
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| CO2019002513A2 (es) | 2019-03-29 |
| JP7165126B2 (ja) | 2022-11-02 |
| ZA201902562B (en) | 2022-12-21 |
| US10611779B2 (en) | 2020-04-07 |
| MX2019003136A (es) | 2019-07-18 |
| ES2904305T3 (es) | 2022-04-04 |
| JP2019529429A (ja) | 2019-10-17 |
| CN118702706A (zh) | 2024-09-27 |
| PH12019500586A1 (en) | 2020-01-20 |
| KR20190047070A (ko) | 2019-05-07 |
| CL2019000714A1 (es) | 2019-08-02 |
| MA46264A (fr) | 2019-07-31 |
| CN109963860A (zh) | 2019-07-02 |
| IL265382A (en) | 2019-05-30 |
| BR112019005323A2 (pt) | 2019-07-02 |
| AU2017328614B2 (en) | 2022-01-13 |
| UY37409A (es) | 2018-04-30 |
| EP3515921A1 (de) | 2019-07-31 |
| US20190248811A1 (en) | 2019-08-15 |
| EP3515921B1 (de) | 2021-10-27 |
| WO2018050825A1 (de) | 2018-03-22 |
| AU2017328614A1 (en) | 2019-04-11 |
| KR102468453B1 (ko) | 2022-11-17 |
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