AR101021A1 - Derivados de 2-amino-5-ceto-piridimina y su uso para combatir el crecimiento indeseado de plantas - Google Patents
Derivados de 2-amino-5-ceto-piridimina y su uso para combatir el crecimiento indeseado de plantasInfo
- Publication number
- AR101021A1 AR101021A1 ARP150102076A ARP150102076A AR101021A1 AR 101021 A1 AR101021 A1 AR 101021A1 AR P150102076 A ARP150102076 A AR P150102076A AR P150102076 A ARP150102076 A AR P150102076A AR 101021 A1 AR101021 A1 AR 101021A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- alkoxy
- cycloalkyl
- cycloalkenyl
- Prior art date
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 25
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical class 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 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
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000006621 (C3-C8) cycloalkyl-(C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000005974 C6-C14 arylcarbonyl group Chemical group 0.000 abstract 2
- 125000005914 C6-C14 aryloxy group Chemical group 0.000 abstract 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000005087 alkynylcarbonyl group Chemical group 0.000 abstract 2
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 abstract 2
- 150000001721 carbon Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000006779 haloalkynylcarbonyl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000006636 (C3-C8) cycloalkylcarbonyl group Chemical group 0.000 abstract 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000005109 alkynylthio group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000005135 aryl sulfinyl group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004465 cycloalkenyloxy group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- 235000019256 formaldehyde Nutrition 0.000 abstract 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 125000006776 haloalkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 1
- 125000006788 haloalkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 1
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- 125000004693 haloalkylthiocarbonyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Su uso en el área de la protección de plantas. Reivindicación 1: Compuestos de la fórmula general (1) y sus sales agroquímicamente compatibles en los cuales R¹ está seleccionado del grupo que se compone de alquilo C₁₋₆, haloalquilo C₁₋₆, alquilcarbonil C₁₋₆-alquilo C₁₋₄; alcoxicarbonil C₁₋₆-alquilo C₁₋₆, haloalcoxicarbonil C₁₋₆-alquilo C₁₋₆, alcoxicarbonil C₁₋₆-haloalquilo C₁₋₆, haloalcoxicarbonil C₁₋₆-haloalquilo C₁₋₆; alquenilo C₂₋₆, haloalquenilo C₂₋₆; alquinilo C₂₋₆, haloalquinilo C₂₋₆; tri-alquilsilil C₁₋₆-alquinilo C₂₋₆, di-alquilsilil C₁₋₆-alquinilo C₂₋₆, mono-alquilsilil C₁₋₆-alquinilo C₂₋₆; fenilsilil-alquinilo C₂₋₆; arilo C₆₋₁₄, los cuales pueden estar sustituidos en cada caso en la parte arilo con halógeno, alquilo C₁₋₆ y/o haloalquilo C₁₋₆; aril C₆₋₁₄-alquilo C₁₋₆; aminocarbonil-alquilo C₁₋₆; alcoxi C₁₋₆-alquilo C₁₋₆; cicloalquilo C₃₋₈, que dado el caso puede estar sustituido en el resto cicloalquilo con alquilo C₁₋₆ y/o halógeno; cicloalquil C₃₋₈-alquilo C₁₋₆, cicloalquil C₃₋₈-haloalquilo C₁₋₆ cicloalquenilo C₃₋₈, cicloalquenil C₃₋₈-alquilo C₁₋₆, cicloalquenil C₃₋₈-haloalquilo C₁₋₆, hidroxi-alquilo C₁₋₆, ciano-alquilo C₁₋₆; alquilsulfonil C₁₋₆-alquilo C₁₋₆, alquiltio C₁₋₆-alquilo C₁₋₆, alquilsulfinil C₁₋₆-alquilo C₁₋₆, haloalquilsulfonil C₁₋₆-alquilo C₁₋₆, haloalquiltio C₁₋₆-alquilo C₁₋₆, haloalquilsulfinil C₁₋₆-alquilo C₁₋₆, alquilsulfonil C₁₋₆-haloalquilo C₁₋₆, alquiltio C₁₋₆-haloalquilo C₁₋₆, alquilsulfinil C₁₋₆-haloalquilo C₁₋₆, haloalquilsulfonil C₁₋₆- haloalquilo C₁₋₆, haloalquiltio C₁₋₆-haloalquilo C₁₋₆, haloalquilsulfinil C₁₋₆-haloalquilo C₁₋₆; y R²ᵃ y R²ᵇ, están seleccionados cada uno independientemente entre sí del grupo que se compone de hidrógeno, halógeno, hidroxi, ciano, nitro, C(O)OH, C(O)NH₂; alquilo C₁₋₆, haloalquilo C₁₋₆, alquilcarbonilo C₁₋₆, haloalquilcarbonilo C₁₋₆, alquilcarboniloxi C₁₋₆, haloalquilcarboniloxi C₁₋₆, alquilcarbonil C₁₋₆-alquilo C₁₋₄; alcoxi C₁₋₆, haloalcoxi C₁₋₆, alcoxicarbonilo C₁₋₆, haloalcoxicarbonilo C₁₋₆, alcoxicarbonil C₁₋₆-alquilo C₁₋₆, haloalcoxicarbonil C₁₋₆-alquilo C₁₋₆, alcoxicarbonil C₁₋₆-haloalquilo C₁₋₆, haloalcoxicarbonil C₁₋₆-haloalquilo C₁₋₆; alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquenilcarbonilo C₂₋₆, haloalquenilcarbonilo C₂₋₆, alqueniloxi C₂₋₆, haloalqueniloxi C₂₋₆, alqueniloxicarbonilo C₂₋₆, haloalqueniloxicarbonilo C₂₋₆; alquinilo C₂₋₆, haloalquinilo C₂₋₆, alquinilcarbonilo C₂₋₆, haloalquinilcarbonilo C₂₋₆, alquiniloxi C₂₋₆, haloalquiniloxi C₂₋₆, alquiniloxicarbonilo C₂₋₆, haloalquiniloxicarbonilo C₂₋₆; tri-alquilsilil C₁₋₆-alquinilo C₂₋₆, di-alquilsilil C₁₋₆-alquinilo C₂₋₆, mono-alquilsilil C₁₋₆-alquinilo C₂₋₆; fenilsilil-alquinilo C₂₋₆; arilo C₆₋₁₄, ariloxi C₆₋₁₄, arilcarbonilo C₆₋₁₄ y ariloxicarbonilo C₆₋₁₄ los cuales pueden estar cada uno sustituidos en la parte arilo con halógeno, alquilo C₁₋₆ y/o haloalquilo C₁₋₆; aril C₆₋₁₄-alquilo C₁₋₆, aril C₆₋₁₄-alcoxi C₁₋₆, aril C₆₋₁₄-alquil C₁₋₆-carbonilo, aril C₆₋₁₄-alquil C₁₋₆-carboniloxi, aril C₆₋₁₄-alcoxicarbonilo C₁₋₆, aril C₆₋₁₄-alcoxicarboniloxi C₁₋₆; aminocarbonil-alquilo C₁₋₆, di-alquilaminocarbonil C₁₋₆-alquilo C₁₋₆; N-(haloalcanoil C₁₋₆)-amino-carbonilo, mono-(aril C₆₋₁₄)-amino-carbonilo, di-(aril C₆₋₁₄)-amino-carbonilo; alcoxi C₁₋₆-alquilo C₁₋₆, alcoxi C₁₋₆-alcoxi C₁₋₆,alcoxicarbonil C₁₋₆-alcoxi C₁₋₆; cicloalquilo C₃₋₈, que dado el caso puede estar sustituido en el resto cicloalquilo con alquilo C₁₋₆ y/o halógeno; cicloalcoxi C₃₋₈, cicloalquil C₃₋₈-alquilo C₁₋₆, cicloalquil C₃₋₈-haloalquilo C₁₋₆, cicloalquil C₃₋₈-alcoxi C₁₋₆, cicloalquil C₃₋₈-haloalcoxi C₁₋₆, cicloalquilcarbonilo C₃₋₈, cicloalcoxicarbonilo C₃₋₈, cicloalquil C₃₋₈-alquilcarbonilo C₁₋₆, cicloalquil C₃₋₈-haloalquilcarbonilo C₁₋₆, cicloalquil C₃₋₈-alcoxicarbonilo C₁₋₆, cicloalquil C₃₋₈-haloalcoxicarbonilo C₁₋₆, cicloalquilcarboniloxi C₃₋₈, cicloalcoxicarboniloxi C₃₋₈, cicloalquil C₃₋₈-alquilcarboniloxi C₁₋₆, cicloalquil C₃₋₈-haloalquilcarboniloxi C₁₋₆, cicloalquil C₃₋₈-alcoxicarboniloxi C₁₋₆, cicloalquil C₃₋₈-haloalcoxicarboniloxi C₁₋₆; cicloalquenilo C₃₋₈, cicloalqueniloxi C₃₋₈, cicloalquenil C₃₋₈-alquilo C₁₋₆, cicloalquenil C₃₋₈-haloalquilo C₁₋₆, cicloalquenil C₃₋₈-alcoxi C₁₋₆, cicloalquenil C₃₋₈-haloalcoxi C₁₋₆, cicloalquenilcarbonilo C₃₋₈, cicloalqueniloxicarbonilo C₃₋₈, cicloalquenil C₃₋₈-alquilcarbonilo C₁₋₆, cicloalquenil C₃₋₈-haloalquilcarbonilo C₁₋₆, cicloalquenil C₃₋₈-alcoxicarbonilo C₁₋₆, cicloalquenil C₃₋₈-haloalcoxicarbonilo C₁₋₆, cicloalquenilcarboniloxi C₃₋₈, cicloalqueniloxicarboniloxi C₃₋₈, cicloalquenil C₃₋₈-alquilcarboniloxi C₁₋₆, cicloalquenil C₃₋₈-haloalquilcarboniloxi C₁₋₆, cicloalquenil C₃₋₈-alcoxicarboniloxi C₁₋₆, cicloalquenil C₃₋₈-haloalcoxicarboniloxi C₁₋₆; hidroxi-alquilo C₁₋₆, hidroxi-alcoxi C₁₋₆ ciano-alcoxi C₁₋₆, ciano-alquilo C₁₋₆; y alquilsulfonilo C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, haloalquilsulfonilo C₁₋₆, haloalquiltio C₁₋₆, haloalquilsulfinilo C₁₋₆, alquilsulfonil C₁₋₆-alquilo C₁₋₆, alquiltio C₁₋₆-alquilo C₁₋₆, alquilsulfinil C₁₋₆-alquilo C₁₋₆, haloalquilsulfonil C₁₋₆-alquilo C₁₋₆, haloalquiltio C₁₋₆-alquilo C₁₋₆, haloalquilsulfinil C₁₋₆-alquilo C₁₋₆, alquilsulfonil C₁₋₆-haloalquilo C₁₋₆, alquiltio C₁₋₆-haloalquilo C₁₋₆, alquilsulfinil C₁₋₆-haloalquilo C₁₋₆, haloalquilsulfonil C₁₋₆-haloalquilo C₁₋₆, haloalquiltio C₁₋₆-haloalquilo C₁₋₆, haloalquilsulfinil C₁₋₆-haloalquilo C₁₋₆, alquilsulfoniloxi C₁₋₆, haloalquilsulfoniloxi C₁₋₆, alquiltiocarbonilo C₁₋₆, haloalquiltiocarbonilo C₁₋₆, alquiltiocarboniloxi C₁₋₆, haloalquiltiocarboniloxi C₁₋₆, alquiltio C₁₋₆-alquilo C₁₋₆, alquiltio C₁₋₆-alcoxi C₁₋₆, alquiltio C₁₋₆-alquilcarbonilo C₁₋₆, alquiltio C₁₋₆-alquilcarboniloxi C₁₋₆; arilsulfonilo C₄₋₁₄, ariltio C₆₋₁₄, arilsulfinilo C₆₋₁₄, cicloalquiltio C₃₋₈, alqueniltio C₃₋₈, cicloalqueniltio C₃₋₈ y alquiniltio C₃₋₆; y R¹ con R²ᵃ pueden estar unidos entre sí mediante un enlace, de modo que junto con los carbonos 4 (o el carbono 6) y 5 de la pirimidina y del grupo carbonilo en la posición 5 de la pirimidina resulta un carbociclo o un heterociclo de 5 a 7 miembros parcialmente hidrogenados que también pueden estar sustituidos; R³ está seleccionado del grupo que se compone de hidrógeno, alquilo C₁₋₆ alcoxi C₁₋₆, alcoxi C₁₋₆-alquilo C₁₋₆, alcoxi C₁₋₆-carbonilo y aminocarbonilo; R⁴ y R⁵, están seleccionados cada uno independientemente entre sí del grupo que se compone de hidrógeno, alquilo C₁₋₆, haloalquilo C₁₋₆, hidroxi, alcoxi C₁₋₆ y haloalcoxi C₁₋₆; o los restos R⁴ y R⁵ juntos con el átomo de carbono al que están unidos, forman un anillo de tres a siete miembros; y R⁶ y R⁷, están seleccionados cada uno independientemente entre sí del grupo que se compone de hidrógeno, alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, arilo C₆₋₁₄, ariloxi C₆₋₁₄, arilcarbonilo C₆₋₁₄ y ariloxicarbonilo C₆₋₁₄; o los restos R⁶ y R⁷ juntos forman un grupo alquileno C₁₋₇ que pueden contener uno o varios átomos de oxígeno y/o de azufre, pudiendo estar el grupo alquileno C₁₋₇ mono o polisustituido con halógeno y los respectivos sustituyentes halógeno pueden ser iguales o diferentes, y n es el número corriente 0, 1 ó 2 y R⁸, R⁹, R¹⁰ y R¹¹, están seleccionados cada uno independientemente entre sí del grupo que se compone de hidrógeno, halógeno, ciano, C(O)OH, C(O)NH₂, alquilo C₁₋₆, alquilcarbonilo C₁₋₆, alquiloxicarbonilo C₁₋₆, alquilaminocarbonilo C₁₋₆, di-alquilaminocarbonilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆,haloalcoxi C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquinilo C₂₋₆, alquinilcarbonilo C₂₋₆, haloalquinilcarbonilo C₂₋₆, alquiniloxi C₂₋₆, haloalquiniloxi C₂₋₆, alquiniloxicarbonilo C₂₋₆, haloalquiniloxicarbonilo C₂₋₆ y nitro; X representa un enlace (en caso que n = 1 o n = 2), CH₂, O, S, carbonilo, NH, CR¹²R¹³ y NR¹⁴ o CH₂O, CH₂S, siendo que en los dos grupos mencionados por último, el átomo de carbono está unido a la parte aromática y el heteroátomo O ó S está unida a la parte parcialmente hidrogenada de la amina; y R¹² y R¹³, están seleccionados cada uno independientemente entre sí del grupo que se compone de hidrógeno, alquilo C₁₋₆ y haloalquilo C₁₋₆; y R¹⁴ está seleccionado del grupo que se compone de hidrógeno, alquilo C₁₋₆ y haloalquilo C₁₋₆.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14175250 | 2014-07-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR101021A1 true AR101021A1 (es) | 2016-11-16 |
Family
ID=51022268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150102076A AR101021A1 (es) | 2014-07-01 | 2015-06-29 | Derivados de 2-amino-5-ceto-piridimina y su uso para combatir el crecimiento indeseado de plantas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US10183914B2 (es) |
| EP (1) | EP3164398B1 (es) |
| JP (1) | JP6629311B2 (es) |
| CN (1) | CN106687448A (es) |
| AR (1) | AR101021A1 (es) |
| AU (1) | AU2015282709A1 (es) |
| BR (1) | BR112016030808A2 (es) |
| CA (1) | CA2953863A1 (es) |
| MX (1) | MX2017000212A (es) |
| WO (1) | WO2016001118A1 (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11477982B2 (en) * | 2017-04-05 | 2022-10-25 | Bayer Cropscience Aktiengesellschaft | 2-amino-5-oxyalkyl-pyrimidine derivatives and their use for controlling undesired plant growth |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4123525A1 (de) | 1991-07-16 | 1993-01-21 | Basf Ag | Substituierte pyrimidinderivate und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
| JPH08183781A (ja) * | 1994-12-28 | 1996-07-16 | Idemitsu Kosan Co Ltd | トリアジン誘導体およびそれを有効成分とする除草剤 |
| EP2206703A1 (de) | 2008-12-30 | 2010-07-14 | Bayer CropScience AG | Pyrimidinderivate und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwachstums |
| GB0725218D0 (en) * | 2007-12-24 | 2008-02-06 | Syngenta Ltd | Chemical compounds |
| EP2210879A1 (de) * | 2008-12-30 | 2010-07-28 | Bayer CropScience AG | Pyrimidinderivate und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwachstums |
| BR112014024203B1 (pt) | 2012-03-29 | 2019-09-03 | Bayer Intellectual Property Gmbh | derivados de 5-aminopirimidina e sua utilização para o controle do crescimento de plantas indesejadas |
-
2015
- 2015-06-29 AR ARP150102076A patent/AR101021A1/es unknown
- 2015-06-29 US US15/321,629 patent/US10183914B2/en active Active
- 2015-06-29 CN CN201580046499.2A patent/CN106687448A/zh active Pending
- 2015-06-29 JP JP2017519970A patent/JP6629311B2/ja not_active Expired - Fee Related
- 2015-06-29 MX MX2017000212A patent/MX2017000212A/es unknown
- 2015-06-29 AU AU2015282709A patent/AU2015282709A1/en not_active Abandoned
- 2015-06-29 BR BR112016030808A patent/BR112016030808A2/pt not_active Application Discontinuation
- 2015-06-29 EP EP15731368.5A patent/EP3164398B1/de not_active Not-in-force
- 2015-06-29 WO PCT/EP2015/064661 patent/WO2016001118A1/de not_active Ceased
- 2015-06-29 CA CA2953863A patent/CA2953863A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN106687448A (zh) | 2017-05-17 |
| US10183914B2 (en) | 2019-01-22 |
| JP6629311B2 (ja) | 2020-01-15 |
| BR112016030808A2 (pt) | 2017-08-22 |
| CA2953863A1 (en) | 2016-01-07 |
| MX2017000212A (es) | 2017-05-01 |
| EP3164398B1 (de) | 2018-06-13 |
| AU2015282709A1 (en) | 2017-01-19 |
| US20170158644A1 (en) | 2017-06-08 |
| JP2017521491A (ja) | 2017-08-03 |
| EP3164398A1 (de) | 2017-05-10 |
| WO2016001118A1 (de) | 2016-01-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR099823A1 (es) | Compuestos bicíclicos de 7 eslabones | |
| AR069489A1 (es) | Derivados de 3-(bencilsulfinil)-5,5-dimetil-4,5-dihidroisoxazol y derivados de 5,5-dimetil-3-[(1h-pirazol-4-ilmetil)sulfinil]-4,5-dihidroisoxazol quirales, proce-dimientos para su preparacion asi como su uso como herbicidas y como re-guladores del crecimiento de las plantas | |
| AR116993A2 (es) | Compuestos heterociclos bicíclicos y sus usos en terapia | |
| AR104618A1 (es) | Herbicidas derivados de compuestos bicíclicos sustituidos con arilo | |
| AR090862A1 (es) | Compuestos de tetrazolinona y su uso para combatir plagas | |
| AR087624A1 (es) | Derivados fenilicos y/o heterociclicos nitrogenados de sulfuro y sulfoxido utiles como pesticidas | |
| AR106100A1 (es) | Compuestos bicíclicos como inhibidores duales atx / ca | |
| AR099122A1 (es) | Derivados de pirimidiniloxi benceno como herbicidas | |
| AR088449A1 (es) | Benzilindazoles sustituidos | |
| AR088029A1 (es) | Compuestos de pirimidina sustituidos, composiciones farmaceuticas que los contienen y uso de los mismos para el tratamiento del dolor, accidentes cerebrovasculares, epilepsia y otras enfermedades del sistema nervioso central | |
| AR097936A1 (es) | Compuestos herbicidas | |
| MX380421B (es) | Compuestos herbicidas de pirimidiniloxi benceno sustituido. | |
| AR107170A1 (es) | Compuestos heterocíclicos tricíclicos condesados como inhibidores de integrasa del vih | |
| AR105322A1 (es) | Heterociclos nitrogenados como pesticidas | |
| AR103265A1 (es) | Compuestos de azolina sustituidos con un sistema de anillos condensado | |
| AR096613A1 (es) | Moduladores de la acetil-coa carboxilasa | |
| AR109346A1 (es) | Derivados de heterociclos bicíclicos condensados como pesticidas | |
| AR103266A1 (es) | Compuestos cíclicos sustituidos con un sistema de anillos condensado para combatir plagas de invertebrados | |
| AR101489A1 (es) | Compuestos reguladores del crecimiento vegetal | |
| AR101906A1 (es) | 1,3,4-tiadiazoles que tienen actividad herbicida, sus composiciones agronómicas y uso relacionado | |
| AR099701A1 (es) | Compuestos heterocíclicos como agentes plaguicidas | |
| AR105460A1 (es) | Derivados sustituidos de 2-pirimidina furano / tienocicloalquilamino y su uso para el control del crecimiento de plantas no deseables | |
| AR101488A1 (es) | Compuestos reguladores del crecimiento vegetal | |
| AR107140A1 (es) | Derivados de 2-amino-5-cetoxim-pirimidina y su uso para combatir crecimiento indeseado de plantas | |
| AR089887A1 (es) | Compuestos fungicidas de pirimidina |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |