CAS: 239110-15-7; Fluopicolide

该化合物是一种合成杀真菌剂,主要用于农业,以控制作物中各种真菌疾病;它属于被称为箱式磷酰胺的化合物类别,具有独特的行动方式,它通过针对线粒体呼吸链,抑制真菌呼吸;这一机制使它能够有效对付微软温和其他宇宙细胞等病原体;氟化二烯酸通常作为一种花生喷雾,因其系统特性而闻名,允许植物吸收并随着时间的推移提供保护;该物质一般被认为对哺乳动物和有益生物具有低毒性,在综合虫害管理战略中成为首选选择;此外,它具有相对较低的环境持久性,有助于其在可持续农业中的有利形象;但是,它应该像所有农药一样,用来标注指示,以尽量减少对非目标生物和环境的潜在风险.

结构式图片

欧盟法规

[欧盟农药活性物质

上下游产品

2,6-Dichlorobenzoyl chloride [3-chloro-5-(trifluoromethyl)-pyridin-2-yl]methanamine hydr°Chloride 2,6-dichloro-benzonitrile (3-chloro-5-(trifluoromethyl)pyridin-2-yl)methanol

合成工艺路线路线简述

    2-(氨甲基)-3-氯-5-三氟甲基吡啶盐酸盐,2,6-二氯苯甲酰氯置于三乙胺体系中,用 乙醇 用作溶剂,化学反应 12.0H,反应生成氟吡菌胺
    参考文献:3-氯-5-三氟甲基-2-吡啶甲胺盐的制备方法
    标题:3-氯-5-三氟甲基-2-吡啶甲胺盐的制备方法
    摘要:本发明公开了一种制备3‑氯‑5‑三氟甲基‑2‑吡啶甲胺盐的方法,该化合物主要用于防治卵菌纲病原菌引起的病害的杀菌剂氟啶酰菌胺合成的中间化合物.本发明的制备方法通过间歇分步反应制取各步中间化工物,最后得到的3‑氯‑5‑三氟甲基‑2‑吡啶甲胺盐化合物和2,6‑二氯苯甲酰氯在有机胺和溶剂存在下反应制得最终目的物氟啶酰菌胺;在制备过程中经过亲核取代反应,亚胺水解和脱羧反应得到目标产物,反应条件温和,操作简单,比较适合工业化生产.

    海关参考信息

    专利信息


    专利号:WO-2025056767-A1
    优先权日:2023-09-15
    标题 :Process for the preparation of enantiomerically enriched aliphatic amines
    发明人:BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
    权利人:SYNGENTA CROP PROTECTION AG
    摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.

    专利号:WO-2024013736-A1
    优先权日:2022-07-12
    标题 :Process for preparing substituted benzamides
    发明人:HAMIRANI BHAVINKUMAR; MAHESH GANDHAM; SREEDEVI MANNAM; PILLAI BIJUKUMAR GOPINATHAN
    权利人:ADAMA MAKHTESHIM LTD
    摘要:The present invention relates to new intermediates for the preparation of pyridylmethylbenzamides via substituted hydroxyiminopyridines or acetamidopyridines, and their innovative preparation processes. The invention discloses, in particular, the total synthesis of fluopicolide fungicide. The preparation of the main substances of the fluopicolide synthesis, specifically, substituted pyridine-2-ylmethanamine or its salt, is disclosed via two different synthesis routes, comprises two novel substances.

    专利号:US-10906880-B2
    优先权日:2016-01-26
    标题:Kind of isothiazole oxime ether-containing strobilurin derivatives and its preparation methods and application
    发明人:FAN ZHIJIN; CHEN LAI; GUO XIAOFENG; ZHU YUJIE; QIAN XIAOLIN; MA LIUYONG; ZHANG NAILOU; WANG HAIXIA; ZHANG ZHIMING; XU JINGHUA; SONG YINQI
    权利人:UNIV NANKAI
    摘要:The present invention is that provided a synthesis method of a series of isothiazole oxime ether containing strobilurin derivatives IV. The present invention relates to 3,4-dichloroisothiazolyl oxime ether strobilurin derivatives, and their chemical structural formula is as shown by IV. n n n n n n n n n n The invention discloses the structural formula of the above compound, the synthesis method and the use as an insecticide, a fungicide, an anti-plant virus agent, and an agriculturally acceptable auxiliary or synergist and a commercial insecticide. The use of a fungicide, an anti-plant virus agent and an acaricide in combination for controlling agricultural, forestry, horticultural plant pests, diseases, virus diseases and preparation methods.

    专利号:US-9968097-B2
    优先权日:2012-05-30
    标题:Composition comprising a biological control agent and a fungicide selected from inhibitors of the lipid membrane synthesis, the melanine biosynthesis, the nucleic acid synthesis or the signal transduction
    发明人:WACHENDORFF-NEUMANN ULRIKE; ANDERSCH WOLFRAM; STENZEL KLAUS; SPRINGER BERND
    权利人:BAYER CROPSCIENCE AG
    摘要:The present invention relates to a composition comprising at least one biological control agent. Furthermore, the present invention relates to the use of this composition as well as a method for reducing overall damage of plants and plant parts.

    专利号:WO-2021074309-A1
    优先权日:2019-10-16
    标 题:1-(3-quinolyl)-3,4-dihydroisoquinoline derivatives as fungicides for combating specific phytopathogens
    发明人:WEISS MATTHIAS; QUARANTA LAURA; BOU HAMDAN FARHAN; MAHAJAN ATUL; WILLIAMS SIMON; KILARU JAGADEESH; SEN INDIRA; BIERI STEPHANE; DIGGELMANN MARTIN
    权利人:SYNGENTA CROP PROTECTION AG
    摘要:1-(3-quinolyl)-3,4-dihydroisoquinoline derivatives of formula (I) as well as a method of combating, preventing or controlling the phytopathogens Mycosphaerella graminicola (Septoria tritici), Fusarium culmorum, Gibberella zeae (Fusarium graminearum) and Monographella nivalis (Microdochium nivale), which comprises applying to the phytopathogen, to the locus of the phytopathogen, or to a plant susceptible to attack by the phytopathogen, or to propagation material thereof, a fungicidally effective amount of a 1-(3-quinolyl)-3,4-dihydroisoquinoline derivative of formula (I). The present description discloses the synthesis of exemplary compounds, formulation examples, relevant biological data (antifungal activity against Mycosphaerella graminicola (Septoria tritici), Fusarium culmorum, Gibberella zeae (Fusarium graminearum) and Monographella nivalis (Microdochium nivale) when spayed on plants), as well as comparative data against three prior art compounds (e.g. pages 52 to 85; formulation examples; examples A1 to A3; table E; compounds E.01 to E.187; biological examples). Exemplary compounds are e.g.: 5-bromo-1-(8-fluoro-3-quinolyl)spiro[4H-isoquinoline-3,1'- cyclopropane] (example A1) 5-bromo-1-(8-fluoro-3-quinolyl)-3,3-dimethyl-4H-isoquinoline (example A2) 1-(8-fluoro-3-quinolyl)-3,3-dimethyl-4H-isoquinoline-5-carbonitrile (example A3)

    专利号:WO-2021074311-A1
    优先权日:2019-10-16
    标题:1-(3-quinolyl)-1,2,3,4-tetrahydroisoquinoline derivatives as fungicides for combating specific phytopathogens
    发明人:WEISS MATTHIAS; QUARANTA LAURA; BOU HAMDAN FARHAN; MAHAJAN ATUL; WILLIAMS SIMON; KILARU JAGADEESH; BIERI STEPHANE; DIGGELMANN MARTIN
    权利人:SYNGENTA CROP PROTECTION AG
    摘要:1-(3-quinolyl)-1,2,3,4-tetrahydroisoquinoline derivatives of formula (I) as well as a method of combating, preventing or controlling the phytopathogens Mycosphaerella graminicola (Septoria tritici), Fusarium culmorum, Gibberella zeae (Fusarium graminearum) and Monographella nivalis (Microdochium nivale), which comprises applying to the phytopathogen, to the locus of the phytopathogen, or to a plant susceptible to attack by the phytopathogen, or to propagation material thereof, a fungicidally effective amount of a 1-(3-quinolyl)-1,2,3,4-tetrahydroisoquinoline derivatives of formula (I). The present description discloses the synthesis of exemplary compounds, formulation examples, relevant biological data (antifungal activity against Mycosphaerella graminicola, Monographella nivalis, Fusarium culmorum and/or Gibberella zeae when spayed on plants) (e.g. pages 47 to 55; examples A1 and A2; compounds E.01 to E.17; table E). An exemplary compounds is e.g.: 3-(5-bromo-3,3-dimethyl-2,4-dihydro-1 H-isoquinolin-1-yl)-8-fluoro- quinoline (example A1)
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    合成参考文献


    摘要:National Pesticide Information Retrieval System's USEPA/OPP Chemical Ingredients Database on Fluopicolide (239110-15-7). Available from, as of July 2, 2018:
    摘要:MacBean C, ed; e-Pesticide Manual. 15th ed., ver. 5.1, Alton, UK; British Crop Protection Council. Fluopicolide (239110-15-7) (2008-2010)
    摘要:California Environmental Protection Agency/Department of Pesticide Regulation; Summary of Toxicology Data on Fluopicolide p.20 (2007). Available from, as of February 4, 2011: California Environmental Protection Agency/Department of Pesticide Regulation; Summary of Toxicology Data on Fluopicolide p.18 (2007). Available from, as of June 28, 2018:
    摘要:USEPA/Office of Pesticide Programs; Environmental Fate and Ecological Risk Assessment for Fluopicolide. p.40 Identification Number: EPA-HQ-OPP-2006-0481-0015 (July 2007). Available from, as of June 28, 2018:
    摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)
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