CAS: 57808-65-8; N-(5-Chloro-4-((4-Chlorophenyl)(Cyano)Methyl)-2-Methylphenyl)-2-Hydroxy-3,5-Diiodobenzamide

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CAS号123-91-1 1,4-二氧六环 | CAS号42016-91-1 3,5-二碘水杨酰氯 | CAS号61437-85-2 2-(4-氨基-2-氯-5-甲...

合成工艺路线路线简述

    对氯苯乙腈置于甲醇,Sodium Methylate,一水合肼,Sodium Hydroxide体系中,用 甲苯,二乙二醇 作为反应溶剂,化学反应 15.0H,反应生成 氯生太尔
    参考文献:氯氰碘柳胺钠的制备方法
    标题:氯氰碘柳胺钠的制备方法
    摘要:本发明公开了一种氯氰碘柳胺钠的制备方法,属于化学药物中间体制备方法技术领域,利用对氯苯乙腈,邻硝基对氯甲苯和2‑羟基‑3,5‑二碘苯甲酸为原料,经缩合反应,还原反应和再缩合反应,然后在氢氧化钠溶液中成盐制备2‑(三氟甲基)吡啶‑3‑甲醛.本发明方法,采用相对友好的还原剂替代铁粉等避免了铁泥和废水等污染物的排放,且简化了后处理,改进后的工艺操作安全简便,反应条件温和,产品收率较高,"三废"少,具有较高的工业化价值.

    海关参考信息

    专利信息


    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)

    专利号:US-10335382-B2
    优先权日:2013-06-14
    标 题:Use of hydrogen sulfide synthesis inhibitors for cancer therapy
    发明人:HELLMICH MARK; ZHOU JIA; SZABO CSABA
    权利人:HELLMICH MARK; ZHOU JIA; SZABO CSABA; UNIV TEXAS
    摘要:In certain aspects the methods comprise administering an inhibitor of hydrogen sulfide biosynthesis, a cystathionine-β-synthase (CBS) inhibitor, or a hydrogen sulfide neutralizing agent to a patient having a cancer associated with elevated production of hydrogen sulfide.

    专利号:WO-2021009026-A1
    优先权日:2019-07-12
    标 题 :Methyl 2-[(4-methoxyimino-tetralin-6-yl]prop-2-enoate derivatives, chromane, isochromane, 6,7,8,9-tetrahydrobenzo[7]annulene, 1h-isobenzofurane and indane analogues thereof, and similar compounds, as agrochemical fungicides
    发明人:WEISS MATTHIAS; WILLIAMS SIMON; RENDINE STEFANO; BOU HAMDAN FARHAN; HOFFMAN THOMAS; QUARANTA LAURA
    权利人:SYNGENTA CROP PROTECTION AG
    摘要:Compounds of formula (I): (Formula (I)) Formula (I) encompasses e.g. tetraline, chromane, isochromane, 6,7,8,9-tetrahydrobenzo[7]annulene, 1H-isobenzofurane and indane derivatives. The compounds of formula (I) are useful as a pesticides, especially as fungicides. The present description discloses the synthesis and characterisation of exemplary compounds as well as biological data thereof (e.g. pages 53 to 78; examples 1 to 10; table T1; compounds 1.1 to 1.54; examples A and B). Preferred compounds are e.g.: Methyl (E)-3-methoxy-2-[(4E)-4-methoxyimino-7-methyl-tetralin-6- yl]prop-2-enoate (example 2; compound 1.6 of table T1): (Formula (A)). Methyl (E)-3-methoxy-2-[(4Z)-4-methoxyiminoisochroman-6-yl]prop-2- enoate (example 6; compound 1.39 of table T1): (Formula (B))

    专利号:WO-2024022910-A1
    优先权日:2022-07-26
    标题 :1-[1-[2-(pyrimidin-4-yl)-1,2,4-triazol-3-yl]ethyl]-3-[2,4-dichloro-5-phenyl]urea derivatives and similar compounds as pesticides
    发明人:WEISS MATTHIAS; JEANGUENAT ANDRE; KILARU JAGADEESH PRATHAP; MUEHLEBACH MICHEL; SCARBOROUGH CHRISTOPHER CHARLES; STOLLER ANDRé; SUESSE LARS
    权利人:SYNGENTA CROP PROTECTION AG
    摘要:The present invention relates to compounds of formula (I) wherein: X is O or S; Q is Q a or Q b as pesticides and insecticides. Preferred compounds are e.g. 1-[1-[2-(pyrimidin-4-yl)-1,2,4-triazol-3-yl]ethyl]-3-[2,4-dichloro-5-phenyl]urea derivatives and similar compounds. An exemplary compound is e.g. 1-[(1S)-1-[2-(6-cyanopyrimidin-4-yl) -1,2,4-triazol-3-yllethyll-3-[2,4-dichloro-5-(trifluoromethyl)phenyllurea (example E1; compound P1). The present invention discloses the synthesis and characterisation of exemplary compounds as well as biological data thereof.

    专利号:US-2014315720-A1
    优先权日:2012-10-24
    标 题 :Polysaccharide ester microspheres and methods and articles relating thereto
    发明人:FALLON DENIS G; GARRETT THOMAS S; KIZER LAWTON E; ZAZZARA KAREN L; COMBS MICHAEL T; JOHNSON RICHARD K; DEHART GARY
    权利人:CELANESE ACETATE LLC
    摘要:A method for producing a polysaccharide ester microsphere may include forming a polysaccharide ester product from a polysaccharide synthesis, wherein the polysaccharide ester product comprises a polysaccharide ester and a solvent; diluting the polysaccharide ester product, thereby yielding a polysaccharide ester dope; and forming a plurality of polysaccharide ester microspheres from the polysaccharide ester dope. Suitable polysaccharides may include, but are not limited to, starch, cellulose, hemicellulose, algenates, chitosan, and any combination thereof. Esters thereof may be organic esters (e.g., acetate and the like), inorganic esters (e.g., sulfonates and the like), or combinations thereof. Further, the solids conent of the polysaccharide ester dope, in some instances, may be greater than about 16 wt %.
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    主要参考文献


    1: Novobilský A, Höglund J. First report of closantel treatment failure against Fasciola hepatica in cattle. Int J Parasitol Drugs Drug Resist. 2015 Aug 28;5(3):172-7. doi: 10.1016/j.ijpddr.2015.07.003. eCollection 2015 Dec.
    2: Snoj T, Cebulj-Kadunc N, Kobal S. Does closantel in therapeutic doses display thyroid hormone-like activity in sheep? J Vet Pharmacol Ther. 2015 Jun;38(3):297-300. doi: 10.1111/jvp.12188. Epub 2014 Nov 20. doi: 10.3109/10837450.2015.1035725. Epub 2015 Aug 31. doi: 10.1016/j.vetpar.2016.08.009. Epub 2016 Aug 5. doi: 10.1016/j.vetpar.2015.10.029. Epub 2015 Nov 10. doi: 10.1001/jamaophthalmol.2015.191. doi: 10.1038/ja.2015.127. Epub 2015 Dec 16.
    9: Solana MV, Mera y Sierra R, Scarcella S, Neira G, Solana HD. In vivo assessment of closantel ovicidal activity in Fasciola hepatica eggs. Exp Parasitol. 2016 Jan;160:49-53. doi: 10.1016/j.exppara.2015.10.010. Epub 2015 Nov 6. doi: 10.1016/j.vetpar.2014.11.016. Epub 2014 Nov 24. doi: 10.1111/jvp.12135. Epub 2014 Jun 6. doi: 10.1016/j.chroma.2014.02.090. Epub 2014 Mar 12. doi: 10.1021/jf4022866. Epub 2013 Aug 30. BMC Ophthalmol. 2016 Nov 29;16(1):207.

    合成参考文献


    摘要:Veterinariya. Veterinary Science., 75(8)(23), 1998
    参考文献:10.1016/s0021-9673(99)00135-1
    摘要:Stoev G, Dakova T, Michailova A. Quantitative determination of Closantel residues in milk by high-performance liquid chromatography with fluorescence detection. J Chromatogr A. 1999 Jun 18;846(1-2):383–6. doi: 10.1016/s0021-9673(99)00135-1.
    参考文献:10.1023/a:1014214122167
    摘要:Keyyu JD, Mahingika HM, Magwisha HB, Kassuku AA. Efficacy of Albendazole and Levamisole against Gastrointestinal Nematodes of Sheep and Goats in Morogoro, Tanzania. Tropical Animal Health and Production. 2002 Mar;34(2):115–20. doi: 10.1023/a:1014214122167.
    参考文献:10.1016/j.ijpddr.2015.07.003
    摘要:Novobilský A, Höglund J. First report of closantel treatment failure against Fasciola hepatica in cattle. International Journal for Parasitology: Drugs and Drug Resistance. 2015 Dec;5(3):172–7. doi: 10.1016/j.ijpddr.2015.07.003.
    参考文献:10.1007/s00436-017-5393-2
    摘要:Venjakob PL, Thiele G, Clausen PH, Nijhof AM. Toxocara vitulorum infection in German beef cattle. Parasitol Res. 2017 Mar;116(3):1085–8. doi: 10.1007/s00436-017-5393-2.
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