AR076610A1 - Compuestos spiro epoxidos como intermediarios - Google Patents

Compuestos spiro epoxidos como intermediarios

Info

Publication number
AR076610A1
AR076610A1 ARP100101855A ARP100101855A AR076610A1 AR 076610 A1 AR076610 A1 AR 076610A1 AR P100101855 A ARP100101855 A AR P100101855A AR P100101855 A ARP100101855 A AR P100101855A AR 076610 A1 AR076610 A1 AR 076610A1
Authority
AR
Argentina
Prior art keywords
alkyl
substituted
haloalkyl
alkoxy
halogen
Prior art date
Application number
ARP100101855A
Other languages
English (en)
Original Assignee
Syngenta Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB0909303A external-priority patent/GB0909303D0/en
Priority claimed from GB0921345A external-priority patent/GB0921345D0/en
Application filed by Syngenta Ltd filed Critical Syngenta Ltd
Publication of AR076610A1 publication Critical patent/AR076610A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/10Spiro-condensed systems
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/16Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D309/28Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D309/30Oxygen atoms, e.g. delta-lactones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/32Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Environmental Sciences (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Pest Control & Pesticides (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pyrane Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Epoxy Compounds (AREA)
  • Furan Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

Los compuestos son intermediarios adecuados en la preparacion de 4-fenil-3,5-pirandionas, 4-fenil-3,5-tiopirandionas y 6-fenilcicIohexan-1,3,5-trionas herbicidamente activas. Reivindicacion 1: Compuestos de la formula (1) donde R1 es halogeno, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4; R2 es hidrogeno, halogeno, metilsulfoniloxi, haloalquilsulfoniloxi C1-4, p-tolilsulfoniloxi, arilo opcionalmente sustituido o heteroarilo opcionalmente sustituido; r es 0, 1, 2 o 3; R3 si r es 1, es alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, ciano o nitro; o los sustituyentes R3, si r es 2 o 3, independientemente entre sí, son alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, ciano o nitro; Y es O, S, SO, SO2 o CO; R4, R5, R6 y R7, independientemente entre sí, son hidrogeno, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 alquilo C1-4, alquiltio C1-4 alquilo C1-4, alquilsulfinilo C1-4 alquilo C1-4, alquilsulfonilo C1-4 alquilo C1-4, ciclopropilo o ciclopropilo sustituido con alquilo C1 o C2, haloalquilo C1 o C2 o halogeno; ciclobutilo o ciclobutilo sustituido con alquilo C1 o C2; oxetanilo u oxetanilo sustituido con alquilo C1 o C2; cicloalquilo C5-7 o cicloalquilo C5-7 sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metileno del resto cicloalquilo se reemplaza opcionalmente por un átomo de oxígeno o azufre o un grupo sulfinilo o sulfonilo; cicloalquenilo C4-7 o cicloalquenilo C4-7 sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metileno del resto cicloalquenilo se reemplaza opcionalmente por un átomo de oxigeno o azufre o un grupo sulfinilo o sulfonilo; ciclopropilalquilo C1-5 o ciclopropilalquilo C1-5 sustituido con alquilo C1 o C2, haloalquilo C1 o C2 o halogeno; ciclobutilalquilo C1-5 o ciclobutilalquilo C1-5 sustituido con alquilo C1 o C2; oxetanilalquilo C1-5 u oxetanilalquilo C1-5 sustituido con alquilo C1 o C2; cicloalquilo C5-7 alquilo C1-5 o cicloalquilo C5-7 alquilo C1-5 sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metilo del resto cicloalquilo se reemplaza opcionalmente por un átomo de oxígeno o azufre o un grupo sulfinilo o sulfonilo; cicloalquenilo C4-7 alquilo C1-5 o cicloalquenilo C4-7 alquilo C1-5 el cual se encuentra sustituido con alquilo C1 o C2 o haloalquilo C1 o C2, donde un grupo metileno del resto cicloalquenilo se reemplaza opcionalmente por un átomo de oxígeno o azufre o un grupo sulfinilo o sulfonilo; fenilo o fenilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4 bencilo o bencilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4 heteroarilo o heteroarilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4; o R4 y R5, o R6 y R7, se unen para formar un anillo saturado o insaturado de 5 - 7 miembros donde un grupo metileno se reemplaza opcionalmente por un átomo de oxígeno o azufre, o un anillo saturado o insaturado de 5 - 7 miembros sustituido con alquilo C1 o C2, donde un grupo metileno del anillo se reemplaza opcionalmente por un átomo de oxígeno o azufre; o R4 y R7 se unen para formar un anillo saturado o insaturado de 5 - 7 miembros no sustituido o sustituido con alquilo C1 o C2, alcoxi C1 o C2, alcoxi C1 o C2 alquilo C1 o C2, hidroxi, halogeno, fenilo o fenilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4 heteroarilo o heteroarilo sustituido con alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, halogeno, nitro, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4 o alquilcarbonilo C1-4.
ARP100101855A 2009-05-29 2010-05-28 Compuestos spiro epoxidos como intermediarios AR076610A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0909303A GB0909303D0 (en) 2009-05-29 2009-05-29 Novel compounds
GB0921345A GB0921345D0 (en) 2009-12-04 2009-12-04 Novel compounds

Publications (1)

Publication Number Publication Date
AR076610A1 true AR076610A1 (es) 2011-06-22

Family

ID=42338979

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP100101855A AR076610A1 (es) 2009-05-29 2010-05-28 Compuestos spiro epoxidos como intermediarios

Country Status (19)

Country Link
US (2) US8680299B2 (es)
EP (1) EP2435415A1 (es)
JP (1) JP5735491B2 (es)
KR (1) KR20120018182A (es)
CN (1) CN102448948B (es)
AP (1) AP2011006038A0 (es)
AR (1) AR076610A1 (es)
AU (1) AU2010252000B2 (es)
BR (1) BRPI1014691A2 (es)
CA (1) CA2763830A1 (es)
CL (1) CL2011003009A1 (es)
CO (1) CO6470820A2 (es)
CU (1) CU20110220A7 (es)
EA (1) EA020243B1 (es)
EC (1) ECSP11011485A (es)
IL (1) IL216364A0 (es)
MX (1) MX2011012533A (es)
TW (1) TW201043608A (es)
WO (1) WO2010136431A1 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101918386B (zh) * 2007-12-13 2013-11-13 辛根塔有限公司 用作除草剂的4-苯基吡喃-3,5-二酮、4-苯基噻喃-3,5-二酮和2-苯基环己-1,3,5-三酮
US8680299B2 (en) * 2009-05-29 2014-03-25 Syngenta Limited Spiro epoxides as intermediates
WO2011073616A2 (en) 2009-12-17 2011-06-23 Syngenta Limited Herbicidal compositions comprising, and methods of use of, herbicidally active pyrandiones
WO2012175899A1 (en) 2011-06-23 2012-12-27 Syngenta Limited Herbicidal composition comprising a pyrandione herbicide and a sulfonyl urea herbicide
GB201310047D0 (en) 2013-06-05 2013-07-17 Syngenta Ltd Compounds
WO2020249691A1 (en) 2019-06-12 2020-12-17 Nouryon Chemicals International B.V. Process for the production of diacyl peroxides
JP7336541B2 (ja) 2019-06-12 2023-08-31 ヌーリオン ケミカルズ インターナショナル ベスローテン フェノーツハップ 過酸化ジアシルを生成するためのプロセス
EP3983340B1 (en) * 2019-06-12 2023-08-02 Nouryon Chemicals International B.V. Method for isolating carboxylic acid from an aqueous side stream
WO2024056517A1 (en) 2022-09-14 2024-03-21 Basf Se Use of an alkylether sulfate for improving the efficacy of herbicides
EP4338592A1 (en) 2022-09-15 2024-03-20 Basf Se Use of compound for improving the efficacy of herbicides

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8680012B2 (en) * 2006-12-14 2014-03-25 Syngenta Crop Protection Llc 4-phenyl-pyrane-3,5-diones,4-phenyl-thiopyrane-3,6-diones and cyclohexanetriones as novel herbicides
GB0704652D0 (en) * 2007-03-09 2007-04-18 Syngenta Participations Ag Novel herbicides
CN101918386B (zh) * 2007-12-13 2013-11-13 辛根塔有限公司 用作除草剂的4-苯基吡喃-3,5-二酮、4-苯基噻喃-3,5-二酮和2-苯基环己-1,3,5-三酮
GB0900641D0 (en) * 2009-01-15 2009-02-25 Syngenta Ltd Novel herbicides
US8680299B2 (en) * 2009-05-29 2014-03-25 Syngenta Limited Spiro epoxides as intermediates

Also Published As

Publication number Publication date
CL2011003009A1 (es) 2012-06-22
JP2012528104A (ja) 2012-11-12
BRPI1014691A2 (pt) 2015-08-25
WO2010136431A9 (en) 2011-03-10
TW201043608A (en) 2010-12-16
EA201101675A1 (ru) 2012-08-30
US8987476B2 (en) 2015-03-24
WO2010136431A1 (en) 2010-12-02
AU2010252000B2 (en) 2014-08-14
US20120077993A1 (en) 2012-03-29
US8680299B2 (en) 2014-03-25
ECSP11011485A (es) 2011-12-30
CN102448948B (zh) 2014-08-13
CN102448948A (zh) 2012-05-09
IL216364A0 (en) 2012-01-31
EA020243B1 (ru) 2014-09-30
CO6470820A2 (es) 2012-06-29
AU2010252000A1 (en) 2011-12-08
AP2011006038A0 (en) 2011-12-31
MX2011012533A (es) 2011-12-14
US20140135508A1 (en) 2014-05-15
EP2435415A1 (en) 2012-04-04
CU20110220A7 (es) 2012-03-15
JP5735491B2 (ja) 2015-06-17
CA2763830A1 (en) 2010-12-02
KR20120018182A (ko) 2012-02-29

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