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AR035947A1 - Derivados sinteticos de 21-butenilespinosina de compuestos relacionados,composiciones insecticidas y acaricidas formuladas con dichos derivados y metodos de aplicacion de los derivados mencionados - Google Patents

Derivados sinteticos de 21-butenilespinosina de compuestos relacionados,composiciones insecticidas y acaricidas formuladas con dichos derivados y metodos de aplicacion de los derivados mencionados

Info

Publication number
AR035947A1
AR035947A1 ARP020101029A ARP020101029A AR035947A1 AR 035947 A1 AR035947 A1 AR 035947A1 AR P020101029 A ARP020101029 A AR P020101029A AR P020101029 A ARP020101029 A AR P020101029A AR 035947 A1 AR035947 A1 AR 035947A1
Authority
AR
Argentina
Prior art keywords
alkylcarbonyl
alkyl
formula
derivatives
group
Prior art date
Application number
ARP020101029A
Other languages
English (en)
Original Assignee
Dow Agrosciences Llc
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
Application filed by Dow Agrosciences Llc filed Critical Dow Agrosciences Llc
Publication of AR035947A1 publication Critical patent/AR035947A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H17/00Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
    • C07H17/04Heterocyclic radicals containing only oxygen as ring hetero atoms
    • C07H17/08Hetero rings containing eight or more ring members, e.g. erythromycins
    • 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
    • A01N45/00Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
    • A01N45/02Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring having three carbocyclic rings
    • 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
    • A01N63/00Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
    • A01N63/30Microbial fungi; Substances produced thereby or obtained therefrom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • A61P33/14Ectoparasiticides, e.g. scabicides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/26Acyclic or carbocyclic radicals, substituted by hetero rings
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Zoology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Veterinary Medicine (AREA)
  • Plant Pathology (AREA)
  • Wood Science & Technology (AREA)
  • Environmental Sciences (AREA)
  • Dentistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Mycology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Saccharide Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Pyrane Compounds (AREA)

Abstract

Se describen y reivindican derivados de síntesis relacionados con la 21-butenilespinosina. Específicamente se trata de fórmula (1), respectivamente de la fórmula (2), donde: R3 es un grupo de las fórmulas (3a) a (3v); R4 es H, OH, OR15, ó =O; R5 es H ó CH3; R6 y R7 son H o se combinan para formar una unión doble o un grupo epoxi; R8 en la fórmula (1) es un butenilo-1-trans, 1,3-butadienilo, n-butilo, 3-hidroxi-1-butenilo, n-propilo, 1-propenilo, 1,2-epoxi-1-butilo, 3-oxo-1-butenilo, ó CH3COR15CH=CH-, y R8 en la fórmula (2) es etilo; R9 es H o un grupo que contiene una de las fórmula (9a) a (9p); R15 es alquilo C2-6, alquilo C3-6 ramificado, cicloalquilo C3-7, alquilo C1-6-alcoxi C1-6, alquilo C1-6-alquiltio C1-6, halo-alquilo C1-6, alquenilo C2-6, formilo, alquinilo C2-6, alquilcarbonilo C1-6 o alquilcarbonilo C3-6 ramificado, cicloalquilcarbonilo C3-7, alquilcarbonilo C1-6-alcoxi C1-6, alquilcarbonilo C1-6 halo, alquenilcarbonilo C2-6, y alquinilcarbonilo C2-6; R16 en la fórmula (9m) es un alquilo C1-6, alquenilo C1-6, formilo, alquilcarbonilo C1-6 o alquilcarbonilo ramificado C3-6; N en la fórmula (9n) es un interger de 1 a 4; siempre que al menos se cumpla una de las siguientes condiciones: a) R3 se selecciona del grupo formado por las fórmulas (3g) a (3v); b) R4 es -OCH3, -OR15 ó =O; c) R6 y R7 son H o R6 y R7 se combinan para formar un grupo epoxi; d) R8 es propilo, n-butilo, 1,2-epoxi-1-butilo; CH3C(O)CH=CH, CH3CH(OCH3)CH=CH ó CH3CH(OR15)CH=CH; e) R9 se selecciona del grupo formado por las fórmulas (9j) a (9p); y siempre que el compuesto 22,23-dihidro-ram-I esté excluido. Dichos compuestos provienen de modificaciones introducidas, vía sintética, en factores que producen ciertas cepas de Saccharopolyspora pogona-LW 107129-NRRL 30141-, o cepas mutantes, que contienen genes inactivados de las O-metiltransferasa que poseen actividad acaricida e insecticida y que resultan útiles en la preparación de compuestos con actividad acaricida e insecticida. Se describen y reivindican además los objetos mencionados en el título.
ARP020101029A 2001-03-21 2002-03-21 Derivados sinteticos de 21-butenilespinosina de compuestos relacionados,composiciones insecticidas y acaricidas formuladas con dichos derivados y metodos de aplicacion de los derivados mencionados AR035947A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US27754601P 2001-03-21 2001-03-21

Publications (1)

Publication Number Publication Date
AR035947A1 true AR035947A1 (es) 2004-07-28

Family

ID=23061327

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP020101029A AR035947A1 (es) 2001-03-21 2002-03-21 Derivados sinteticos de 21-butenilespinosina de compuestos relacionados,composiciones insecticidas y acaricidas formuladas con dichos derivados y metodos de aplicacion de los derivados mencionados

Country Status (12)

Country Link
EP (1) EP1370566B1 (es)
JP (1) JP4346310B2 (es)
KR (1) KR100904942B1 (es)
CN (1) CN100354293C (es)
AR (1) AR035947A1 (es)
AU (1) AU2008202480B2 (es)
DK (1) DK1370566T3 (es)
ES (1) ES2634110T3 (es)
IL (1) IL157975A0 (es)
MX (1) MXPA03008505A (es)
TW (1) TWI275592B (es)
WO (1) WO2002077004A1 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2496940T3 (es) * 2001-03-21 2014-09-22 Dow Agrosciences, Llc Derivados plaguicidas de las espinosinas
AR033022A1 (es) * 2001-03-30 2003-12-03 Dow Agrosciences Llc Genes biosinteticos para la produccion de insecticida de butenilespinosina
DK1492404T3 (da) * 2002-02-19 2012-04-23 Dow Agrosciences Llc Nye spinosyndannende polyketidsyntaser
DE10320505A1 (de) 2003-05-08 2004-11-25 Bayer Healthcare Ag Mittel zum Bekämpfen von Parasiten an Tieren
CN101535330B (zh) * 2006-11-03 2012-06-27 陶氏益农公司 选择性还原多杀菌素因子et-j和et-l制备多虫菌素
CN102202506B (zh) * 2008-09-22 2015-07-29 克里斯廷·克里蒂考 刺糖多孢菌素防污组合物、其使用方法、以及受到保护而免于附着污损生物的制品
CN102190694B (zh) * 2010-03-12 2015-09-09 中南大学 多杀菌素衍生物、制备方法及其作为杀虫剂的用途
AU2010101148C4 (en) * 2010-10-19 2015-01-22 Dow Agrosciences Llc Methods of controlling pests
CN102977166B (zh) * 2012-12-05 2015-07-29 湖南化工研究院 13-硫醚取代多杀菌素衍生物及其制备方法
CA2997499A1 (en) 2015-09-03 2017-03-09 Agrimetis, Llc Spinosyn derivatives as insecticides
BR102017003580B1 (pt) * 2016-03-04 2022-03-29 Dow Agrosciences Llc Sistema e processos para produzir spinetoram
CN110191888A (zh) * 2017-01-13 2019-08-30 阿格里麦蒂斯有限责任公司 氮丙啶多杀菌素衍生物和制备方法
EP4079744B1 (en) 2021-04-23 2025-08-06 Acies Bio d.o.o. Novel spinosyn compounds and their use as a pesticide
CN117255794A (zh) * 2021-04-23 2023-12-19 阿西耶斯生物公司 新型刺糖菌素前药
CA3216243A1 (en) 2021-04-23 2022-10-27 Acies Bio D.O.O. Novel spinosyn prodrugs
EP4101858A1 (en) 2021-06-08 2022-12-14 Acies Bio d.o.o. Novel spinosyn compounds

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE5591A1 (es) * 1988-12-19 1991-02-15 Lilly Co Eli Un nuevo grupo de compuestos de macrolida
US6001981A (en) 1996-06-13 1999-12-14 Dow Agrosciences Llc Synthetic modification of Spinosyn compounds
MXPA02002571A (es) * 1999-09-13 2002-10-24 Dow Agrosciences Llc Macrolidas pesticidas.
ES2496940T3 (es) * 2001-03-21 2014-09-22 Dow Agrosciences, Llc Derivados plaguicidas de las espinosinas

Also Published As

Publication number Publication date
ES2634110T3 (es) 2017-09-26
AU2008202480B2 (en) 2011-09-01
EP1370566B1 (en) 2017-04-19
WO2002077004A1 (en) 2002-10-03
KR20030085019A (ko) 2003-11-01
JP4346310B2 (ja) 2009-10-21
EP1370566A1 (en) 2003-12-17
MXPA03008505A (es) 2004-06-30
CN1531543A (zh) 2004-09-22
JP2004530665A (ja) 2004-10-07
AU2008202480A1 (en) 2008-06-26
CN100354293C (zh) 2007-12-12
IL157975A0 (en) 2004-03-28
TWI275592B (en) 2007-03-11
DK1370566T3 (en) 2017-07-24
KR100904942B1 (ko) 2009-06-29

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