AR072317A1 - DIXID OXO AZINIL ISOXAZOLINAS HERBICIDES OF SIX MEMBERS - Google Patents
DIXID OXO AZINIL ISOXAZOLINAS HERBICIDES OF SIX MEMBERSInfo
- Publication number
- AR072317A1 AR072317A1 ARP090102358A AR072317A1 AR 072317 A1 AR072317 A1 AR 072317A1 AR P090102358 A ARP090102358 A AR P090102358A AR 072317 A1 AR072317 A1 AR 072317A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- 7alkyl
- halogen
- independently
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 10
- 150000002367 halogens Chemical group 0.000 abstract 10
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 5
- 125000002837 carbocyclic group Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 abstract 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 1
- 125000005085 alkoxycarbonylalkoxy group Chemical group 0.000 abstract 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 1
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 1
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 1
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000005145 cycloalkylaminosulfonyl group Chemical group 0.000 abstract 1
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl 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
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004992 haloalkylamino group Chemical group 0.000 abstract 1
- 125000006809 haloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004661 haloalkylaminosulfonyl 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
- 125000006769 halocycloalkoxy group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Composiciones que contienen los compuestos de formula 1 y métodos para controlar la vegetacion indeseable que comprenden poner en contacto la vegetacion indeseable o su ambiente con una cantidad eficaz de un compuesto o una composicion de la solicitud. Reivindicacion 1: Un compuesto caracterizado porque se selecciona entre formula 1, N-oxidos y sales del mismo donde J es como en formulas (2), (3) (4) o (5); Q1 es N o CR9a; Q2 es N o CR9b; Q3 es N o CR9c; Q4 es N o CR9d; W1 es N o CR10a; W2 es N o CR10b; con la condicion de que cuando Q2 es N, luego W2 es CR10b; W3 es N o CR10c; W4 es N o CR10d; Y1 es N o CR11a; con la condicion de que cuando W1 es N, luego Y1 es CR11a; Y2 es N o CR11b; con la condicion de que cuando W2 es N, luego Y2 es CR11b; Y3 es N o CR11c, con la condicion de que cuando W3 es N, luego Y3 es CR11c; Y4 es N o CR11d; m es 0, 1 o 2; n es o 1; con la condicion de que la suma de n y m es no más que 2; R1 y R2 son independientemente H, alquilo C1-6, alquenilo C2-C6, alquinilo C2-6, cicloalquilo C3-6, haloalquilo C1-6, haloalquenilo C2-6, alquilcicloalquilo C4-6 o cicloalquilalquilo C4-6; o R1 y R2 se toman juntos con el carbono al cual se encuentran unidos para formar un anillo carbocíclico saturado C3-6 opcionalmente sustituido con alquilo C1-3, halogeno o haloalquilo C1-3; R3 es H, alquilo C1-6, alquenilo C2-C6, alquinilo C2-6, cicloalquilo C3-6, haloalquilo C1-6, haloalquenilo C2-6, alquilcicloalquilo C4-6 o cicloalquilalquilo C4-6; alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, haloalquiltio C1-6, -SCN, halogeno, ciano, nitro, azido, -CO2H o alcoxicarbonilo C2-5; R4 es H, alquilo C1-6, haloalquilo C1-6 o halogeno; o R3 y R4 se toman juntos con el carbono al cual se encuentran unidos para formar un anillo carbocíclico saturado C3-6 opcionalmente sustituido con alquilo C1-3, halogeno o haloalquilo C1-3; o R1 y R4 se toman juntos con los carbonos a los cuales se encuentran unidos para formar un anillo carbocíclico saturado C3-7 opcionalmente sustituido con alquilo C1-3, halogeno o haloalquilo C1-3; R5 es H, alquilo C1-2, halogeno, ciano o alcoxicarbonilo C2-5; R6 es H, alquilo C1-2 o halogeno; o R5 y R6 se toman juntos con el carbono al cual se encuentran unidos para formar un anillo carbocíclico saturado C3-6; R7 es H, -CN, alcoxicarbonilo C2-4, alquilsulfonilo C1-4, alquilcarbonilo C2-4 o haloalquilcarbonilo C2-4; cada R8a, R8b, R8c y R8d es independientemente alquilo C1-7, alquenilo C2-7, alquinilo C2-7, cicloalquilo C3-7, haloalquilo C1-7, haloalquenilo C2-7, alcoxialquilo C2-7, cicloalquilalquilo C4-7, haloalquinilo C3-7, alquilcarbonilalquilo C3-7, alcoxicarbonilalquilo C3-7, halocicloalquilalquilo C4-7, haloalcoxialquilo C2-7, alquiltioalquilo C2-7, alquilsulfonilalquilo C2-7, alquilsulfinilalquilo C2-7, cianoalquilo C2-7, haloalquiltioalquilo C2-7, haloalquilsulfonilalquilo C2-7, haloalquilsulfinilalquilo C2-7, haloalcoxicarbonilalquilo C3-7, haloalquilcarbonilalquilo C3-7, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6 o cicloalquilsulfonilo C3-6; y cada R9a, R9b, R9c, R9d, R10a, R10b, R10c, R10d, R11a, R11b, R11c y R11d es independientemente H, halogeno, ciano, alquilo C1-7, alquenilo C2-7, alquinilo C2-7, cicloalquilo C3-7, cicloalquilalquilo C4-7, alquilcicloalquilo C4-7, haloalquilo C1-7, haloalquenilo C2-7, haloalquinilo C3-7, halocicloalquilo C3-7, alcoxi C1-7, haloalcoxi C1-7, alqueniloxi C2-7, haloalqueniloxi C2-7, cicloalcoxi C3-7, halocicloalcoxi C3-7, alquiniloxi C2-7, cicloalquilalcoxi C4-7, halocicloalquilalcoxi C4-7, alquiltio C1-7, haloalquiltio C1-7, haloalquilsulfinilo C1-7, haloalquilsulfonilo C1-7, alquilamino C1-6, dialquilamino C2-7, haloalquilamino C1-7, alquilcarbonilo C2-7, alcoxicarbonilo C2-7, haloalquilcarbonilo C2-7, haloalcoxicarbonilo C2-7, alquilcarbonilalquilo C3-7, alcoxicarbonilalquilo C3-7, aminocarbonilo, alquilaminocarbonilo C2-8, haloalquilaminocarbonilo C2-8, dialquilaminocarbonilo C3-8, haloalquil(alquil)aminocarbonilo C3-8, cicloalquilaminocarbonilo C4-7, cicloalquil(alquil)aminocarbonilo C5-8, halocicloalquilalquilo C4-7, alcoxialquilo C2-7, haloalcoxialquilo C2-7, alquiltioalquilo C2-7, alquilsulfonilalquilo C2-7, alquilsulfinilalquilo C2-7, cianoalquilo C2-7, haloalquiltioalquilo C2-7, haloalquilsulfonilalquilo C2-7, haloalquilsulfinilalquilo C2-7, haloalcoxicarbonilalquilo C3-7, haloalquilcarbonilalquilo C3-7, alcoxialcoxi C2-7, haloalcoxialcoxi C2-7, alquiltioalcoxi C2-7, haloalquiltioalcoxi C2-7, haloalquilsulfonilalcoxi C2-7, haloalquilsulfinilalcoxi C2-7, nitro, trialquilsililo C3-10, aminosulfonilo, alquilaminosulfonilo C1-7, haloalquilaminosulfonilo C1-7, dialquilaminosulfonilo C2-8, haloalquil(alquil)aminosulfonilo C3-8, cicloalquilaminosulfonilo C3-6 o cicloalquil(alquil)aminosulfonilo C4-7 o Z; cada Z es independientemente -ON=CR12R13, -C(=NOR14)R15, cianoalcoxi C2-6, alcoxihaloalquilo C2-6 o alcoxicarbonilalcoxi C3-7; o fenilo opcionalmente sustituidos con hasta dos sustituyentes seleccionados entre R16; o anillo heterocíclico de 5 o 6 miembros opcionalmente sustituidos con hasta dos sustituyentes seleccionados entre R17 sobre carbonos miembros del anillo y R18 sobre nitrogenos miembros del anillo; cada R12 es independientemente H o alquilo C1-6; cada R13 es independientemente H, alquilo C1-6 o alcoxi C1-4; o un par de R12 y R13 en una instancia de -ON=CR12R13 se toman juntos como -(CH2)2-, -(CH2)3-, -(CH2)4- o -(CH2)5-; cada R14 y R15 es independientemente H o alquilo C1-4; o un par de R14 y R15 en una instancia de -C(=NOR14)R15 se toman juntos como -(CH2)2-, -(CH2)3- o -(CH2)4-; cada R16 es independientemente alquilo C1-6, halogeno, alcoxi C1-4, haloalquilo C1-4 o haloalcoxi C1-4; cada R17 es independientemente alquilo C1-6, halogeno, alcoxi C1-4, haloalquilo C1-4 o haloalcoxi C1-4; y cada R18 es independientemente alquilo C1-6.Compositions containing the compounds of formula 1 and methods for controlling undesirable vegetation comprising contacting undesirable vegetation or its environment with an effective amount of a compound or a composition of the application. Claim 1: A compound characterized in that it is selected from formula 1, N-oxides and salts thereof wherein J is as in formulas (2), (3) (4) or (5); Q1 is N or CR9a; Q2 is N or CR9b; Q3 is N or CR9c; Q4 is N or CR9d; W1 is N or CR10a; W2 is N or CR10b; with the proviso that when Q2 is N, then W2 is CR10b; W3 is N or CR10c; W4 is N or CR10d; Y1 is N or CR11a; with the proviso that when W1 is N, then Y1 is CR11a; Y2 is N or CR11b; with the proviso that when W2 is N, then Y2 is CR11b; Y3 is N or CR11c, with the proviso that when W3 is N, then Y3 is CR11c; Y4 is N or CR11d; m is 0, 1 or 2; n is or 1; with the proviso that the sum of n and m is no more than 2; R1 and R2 are independently H, C1-6 alkyl, C2-C6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, C1-6 haloalkyl, C2-6 haloalkenyl, C4-6 alkylcycloalkyl or C4-6 cycloalkylalkyl; or R1 and R2 are taken together with the carbon to which they are attached to form a C3-6 saturated carbocyclic ring optionally substituted with C1-3 alkyl, halogen or C1-3 haloalkyl; R3 is H, C1-6 alkyl, C2-C6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, C1-6 haloalkyl, C2-6 haloalkenyl, C4-6 alkylcycloalkyl or C4-6 cycloalkylalkyl; C1-6 alkoxy, C1-6 haloalkoxy, C1-6 alkylthio, C1-6 haloalkylthio, -SCN, halogen, cyano, nitro, azido, -CO2H or C2-5 alkoxycarbonyl; R4 is H, C1-6 alkyl, C1-6 haloalkyl or halogen; or R3 and R4 are taken together with the carbon to which they are attached to form a C3-6 saturated carbocyclic ring optionally substituted with C1-3 alkyl, halogen or C1-3 haloalkyl; or R1 and R4 are taken together with the carbons to which they are attached to form a C3-7 saturated carbocyclic ring optionally substituted with C1-3 alkyl, halogen or C1-3 haloalkyl; R5 is H, C1-2 alkyl, halogen, cyano or C2-5 alkoxycarbonyl; R6 is H, C1-2 alkyl or halogen; or R5 and R6 are taken together with the carbon to which they are attached to form a C3-6 saturated carbocyclic ring; R7 is H, -CN, C2-4 alkoxycarbonyl, C1-4 alkylsulfonyl, C2-4 alkylcarbonyl or C2-4 haloalkylcarbonyl; each R8a, R8b, R8c and R8d is independently C1-7 alkyl, C2-7 alkenyl, C2-7 alkynyl, C3-7 cycloalkyl, C1-7 haloalkyl, C2-7 haloalkenyl, C2-7 alkoxyalkyl, C4-7 cycloalkylalkyl, C3-7 haloalkynyl, C3-7 alkylcarbonylalkyl C3-7 alkoxycarbonylalkyl C4-7 alkyl, C2-7 haloalkoxyalkyl, C2-7 alkylthioalkyl, C2-7 alkylsulfonylalkylC2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl, C2-7alkyl C2-7 haloalkylsulfonylalkyl, C2-7 haloalkylsulfinylalkyl, C3-7 haloalkoxycarbonylalkyl C3-7 alkyl, C1-6 alkylsulfonyl, C1-6 haloalkylsulfonyl or C3-6 cycloalkylsulfonyl; and each R9a, R9b, R9c, R9d, R10a, R10b, R10c, R10d, R11a, R11b, R11c and R11d is independently H, halogen, cyano, C1-7 alkyl, C2-7 alkenyl, C2-7 alkynyl, C3 cycloalkyl -7, C4-7 cycloalkylalkyl, C4-7 alkylcycloalkyl, C1-7 haloalkyl, C2-7 haloalkenyl, C3-7 haloalkenyl, C3-7 halocycloalkyl, C1-7 alkoxy, C1-7 haloalkoxy, C2-7 alkenyloxy -7, C3-7 cycloalkoxy, C3-7 halocycloalkoxy, C2-7 alkynyloxy, C4-7 cycloalkylalkoxy, C4-7 halocycloalkylalkoxy, C1-7 alkylthio, C1-7 haloalkylthio, C1-7 haloalkylsulfinyl, C1-7 haloalkylsulfonyl, -6, C2-7 dialkylamino, C1-7 haloalkylamino, C2-7 alkylcarbonyl, C2-7 alkoxycarbonyl, C2-7 haloalkylcarbonyl, C2-7 haloalkoxycarbonyl, C3-7 alkylcarbonylalkyl, C3-7 alkoxycarbonyl, C2- alkylaminocarbonyl C2-8 haloalkylaminocarbonyl, C3-8 dialkylaminocarbonyl, C3-8 haloalkyl (alkyl) aminocarbonyl, C4-7 cycloalkylaminocarbonyl, cycloalkyl (alkyl) aminocarbonyl C5-8, C4-7 I halocycloalkylalkyl, C2-7 alkoxyalkyl, haloalkoxyalkyl C2-7, C2-7 alkylthioalkyl, C2-7 alkylsulfonylalkyl, alkylsulfinylalkyl C2-7, C2-7 cyanoalkyl, haloalquiltioalquilo C2-7, C2-7 haloalquilsulfonilalquilo, haloalquilsulfinilalquilo C2-7, haloalkoxycarbonylalkyl C3-7, haloalkylcarbonylalkyl C3-7, alkoxyalkoxy C2-7, haloalkoxyalkoxy C2-7, alkylthioalkoxy C2-7, haloalkylthioalkoxy C2-7, haloalkylsulfonylalkyl alkoxy C2-7yl, alkylalkyl-C3-7 alkylalkyl-C3-7-alkyl , aminosulfonyl, C1-7 alkylaminosulfonyl, C1-7 haloalkylaminosulfonyl, C2-8 dialkylaminosulfonyl, C3-8 haloalkyl (alkyl) aminosulfonyl, C3-6 cycloalkylaminosulfonyl or C4-7 or cycloalkyl (alkyl) aminosulfonyl; each Z is independently -ON = CR12R13, -C (= NOR14) R15, C2-6 cyanoalkoxy, C2-6 alkoxyhaloalkyl or C3-7 alkoxycarbonylalkoxy; or phenyl optionally substituted with up to two substituents selected from R16; or 5- or 6-membered heterocyclic ring optionally substituted with up to two substituents selected from R17 on ring member carbons and R18 on ring member nitrogen; each R12 is independently H or C1-6 alkyl; each R13 is independently H, C1-6 alkyl or C1-4 alkoxy; or a pair of R12 and R13 in an instance of -ON = CR12R13 are taken together as - (CH2) 2-, - (CH2) 3-, - (CH2) 4- or - (CH2) 5-; each R14 and R15 is independently H or C1-4 alkyl; or a pair of R14 and R15 in an instance of -C (= NOR14) R15 are taken together as - (CH2) 2-, - (CH2) 3- or - (CH2) 4-; each R16 is independently C1-6 alkyl, halogen, C1-4 alkoxy, C1-4 haloalkyl or C1-4 haloalkoxy; each R17 is independently C1-6 alkyl, halogen, C1-4 alkoxy, C1-4 haloalkyl or C1-4 haloalkoxy; and each R18 is independently C1-6 alkyl.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7549508P | 2008-06-25 | 2008-06-25 | |
| US8660408P | 2008-08-06 | 2008-08-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR072317A1 true AR072317A1 (en) | 2010-08-18 |
Family
ID=41045240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090102358 AR072317A1 (en) | 2008-06-25 | 2009-06-25 | DIXID OXO AZINIL ISOXAZOLINAS HERBICIDES OF SIX MEMBERS |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR072317A1 (en) |
| UY (1) | UY31932A (en) |
| WO (1) | WO2009158258A1 (en) |
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| US8962584B2 (en) | 2009-10-14 | 2015-02-24 | Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. | Compositions for controlling Varroa mites in bees |
| CN102822350B (en) | 2010-03-08 | 2015-05-06 | 孟山都技术公司 | Polynucleotide molecules for gene regulation in plants |
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| WO2013039990A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control |
| US10240161B2 (en) | 2012-05-24 | 2019-03-26 | A.B. Seeds Ltd. | Compositions and methods for silencing gene expression |
| US9073878B2 (en) | 2012-11-21 | 2015-07-07 | Zenith Epigenetics Corp. | Cyclic amines as bromodomain inhibitors |
| US9765039B2 (en) | 2012-11-21 | 2017-09-19 | Zenith Epigenetics Ltd. | Biaryl derivatives as bromodomain inhibitors |
| CA2895905A1 (en) | 2012-12-21 | 2014-06-26 | Zenith Epigenetics Corp. | Novel heterocyclic compounds as bromodomain inhibitors |
| CA2896762A1 (en) | 2013-01-01 | 2014-07-10 | A.B. Seeds Ltd. | Methods of introducing dsrna to plant seeds for modulating gene expression |
| US10683505B2 (en) | 2013-01-01 | 2020-06-16 | Monsanto Technology Llc | Methods of introducing dsRNA to plant seeds for modulating gene expression |
| CA2905104A1 (en) | 2013-03-13 | 2014-10-09 | Monsanto Technology Llc | Control of lolium species by topical application of herbicidal composition comprising dsrna |
| AU2014249015B2 (en) | 2013-03-13 | 2020-04-16 | Monsanto Technology Llc | Methods and compositions for weed control |
| US10568328B2 (en) | 2013-03-15 | 2020-02-25 | Monsanto Technology Llc | Methods and compositions for weed control |
| WO2015004533A2 (en) | 2013-06-21 | 2015-01-15 | Zenith Epigenetics Corp. | Novel substituted bicyclic compounds as bromodomain inhibitors |
| PL3010503T3 (en) | 2013-06-21 | 2020-08-24 | Zenith Epigenetics Ltd. | Novel bicyclic bromodomain inhibitors |
| US9850496B2 (en) | 2013-07-19 | 2017-12-26 | Monsanto Technology Llc | Compositions and methods for controlling Leptinotarsa |
| PL3030663T3 (en) | 2013-07-19 | 2020-04-30 | Monsanto Technology Llc | Compositions and methods for controlling leptinotarsa |
| EP3027604B1 (en) | 2013-07-31 | 2019-02-20 | Zenith Epigenetics Ltd. | Novel quinazolinones as bromodomain inhibitors |
| PL3066200T3 (en) | 2013-11-04 | 2025-03-31 | Greenlight Biosciences, Inc. | Compositions and methods for controlling arthropod parasite and pest infestations |
| UA119253C2 (en) | 2013-12-10 | 2019-05-27 | Біолоджикс, Інк. | METHOD FOR VARROA TREATMENT AND VEGETABLES |
| AR099092A1 (en) | 2014-01-15 | 2016-06-29 | Monsanto Technology Llc | METHODS AND COMPOSITIONS FOR WEED CONTROL USING EPSPS POLYUCLEOTIDES |
| EP3420809A1 (en) | 2014-04-01 | 2019-01-02 | Monsanto Technology LLC | Compositions and methods for controlling insect pests |
| CN106795515B (en) | 2014-06-23 | 2021-06-08 | 孟山都技术公司 | Compositions and methods for regulating gene expression via RNA interference |
| EP3161138A4 (en) | 2014-06-25 | 2017-12-06 | Monsanto Technology LLC | Methods and compositions for delivering nucleic acids to plant cells and regulating gene expression |
| AR101348A1 (en) | 2014-07-29 | 2016-12-14 | Monsanto Technology Llc | COMPOSITIONS AND METHODS FOR PEST CONTROL BY INSECTS |
| US10710992B2 (en) | 2014-12-01 | 2020-07-14 | Zenith Epigenetics Ltd. | Substituted pyridinones as bromodomain inhibitors |
| EP3227280B1 (en) | 2014-12-01 | 2019-04-24 | Zenith Epigenetics Ltd. | Substituted pyridines as bromodomain inhibitors |
| CN107207474B (en) | 2014-12-11 | 2021-05-07 | 恒翼生物医药科技(上海)有限公司 | Substituted heterocycles as bromodomain inhibitors |
| US10231953B2 (en) | 2014-12-17 | 2019-03-19 | Zenith Epigenetics Ltd. | Inhibitors of bromodomains |
| UA124255C2 (en) | 2015-01-22 | 2021-08-18 | Монсанто Текнолоджі Елелсі | INSECTICIDAL COMPOSITION AND METHOD OF CONTROL OF LEPTINOTARSA |
| UY36703A (en) | 2015-06-02 | 2016-12-30 | Monsanto Technology Llc | COMPOSITIONS AND METHODS FOR THE ADMINISTRATION OF A POLINUCLEOTIDE ON A PLANT |
| WO2016196782A1 (en) | 2015-06-03 | 2016-12-08 | Monsanto Technology Llc | Methods and compositions for introducing nucleic acids into plants |
| MY202046A (en) * | 2018-09-27 | 2024-03-30 | Fmc Corp | Intermediates for Preparing Herbicidal Pyridazinones |
| KR20230053729A (en) * | 2019-10-31 | 2023-04-21 | 구미아이 가가쿠 고교 가부시키가이샤 | Herbicide and production method for intermediate thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4465133B2 (en) * | 2001-02-08 | 2010-05-19 | クミアイ化学工業株式会社 | Isoxazoline derivatives and herbicides containing the same as active ingredients |
| DE60238194D1 (en) * | 2001-06-21 | 2010-12-16 | Kumiai Chemical Industry Co | ISOXAZOLINE DERIVATIVES AND HERBICIDES |
| UA78071C2 (en) * | 2002-08-07 | 2007-02-15 | Kumiai Chemical Industry Co | Herbicidal composition |
| ES2338135T3 (en) * | 2004-09-03 | 2010-05-04 | Syngenta Limited | ISOXAZOLINE DERIVATIVES AND ITS USE AS HERBICIDES. |
| PL1799657T3 (en) * | 2004-10-05 | 2010-05-31 | Syngenta Ltd | Isoxazoline derivatives and their use as herbicides |
| DE102005031412A1 (en) * | 2005-07-06 | 2007-01-11 | Bayer Cropscience Gmbh | 3- [1-Halo-1-aryl-methane-sulfonyl] and 3- [1-halo-1-heteroaryl-methanesulfonyl] -isoxazoline derivatives, processes for their preparation and use as herbicides and plant growth regulators |
| GB0526044D0 (en) * | 2005-12-21 | 2006-02-01 | Syngenta Ltd | Novel herbicides |
-
2009
- 2009-06-18 WO PCT/US2009/047725 patent/WO2009158258A1/en not_active Ceased
- 2009-06-23 UY UY0001031932A patent/UY31932A/en not_active Application Discontinuation
- 2009-06-25 AR ARP090102358 patent/AR072317A1/en unknown
Also Published As
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|---|---|
| UY31932A (en) | 2010-01-29 |
| WO2009158258A1 (en) | 2009-12-30 |
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