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    • 49. 发明授权
    • Heteroaryl substituted hydroxyphenyltriazine uv-absorbers
    • 杂芳基取代的羟基苯基三嗪紫外线吸收剂
    • US06835329B2
    • 2004-12-28
    • US10398040
    • 2003-03-31
    • Dieter ReinehrHanspeter SauterRudolf Zink
    • Dieter ReinehrHanspeter SauterRudolf Zink
    • C07D25124
    • C07D403/10A61K8/4966A61Q17/04C07D413/10C08K5/3492
    • The present invention provides compounds having the formula (1) in which each of the radicals R1, R2, R3 and R4, independently, represent hydrogen, hydroxy, halogen, C1-C20-alkyl, C1-C20-alkoxy, CN or COOR5, in which R5 is C1-C20-alkyl and Z represents a heterocyclic residue selected from the 2H-benzo[1,2-d]triazol-2-yl, 2H-naphtho[1,2-d]triazol-2-yl, benzimidazol-2-yl, benzoxazol-2-yl and benzofuran-2-yl moieties, optionally substituted by C1-C4-alkyl, C1-C4-alkoxy, halogen or NHCOC1-C4-alkyl, a process for their preparation, new intermediate benzoxazinones useful for their preparation and use of the compounds of formula (1) as UV-absorbers which have improved absorption spectrum characteristics, superior resistance to exposure to UV light and excellent thermal stability, relative to known triphenyltriazine compounds.
    • 本发明提供具有式(1)的化合物,其中每个基团R 1,R 2,R 3和R 4独立地代表氢,羟基,卤素,C 1 -C 20 - 烷基,C 1 -C 20 - 烷氧基,CN或COOR 5, 其中R 5是C 1 -C 20 - 烷基,Z代表选自2H-苯并[1,2-d]三唑-2-基,2H-萘并[1,2-d]三唑-2-基的杂环残基, 苯并恶唑-2-基和苯并呋喃-2-基部分,任选被C 1 -C 4 - 烷基,C 1 -C 4 - 烷氧基,卤素或NHCOC 1 -C 4 - 烷基取代,其制备方法,新中间体 苯并恶嗪酮可用于制备和使用式(1)化合物作为UV吸收剂,其相对于已知的三苯基三嗪化合物具有改进的吸收光谱特征,优异的耐紫外线性和耐热稳定性。
    • 50. 发明授权
    • Process for the preparation of halogenated hydroxydiphenyl compounds
    • 卤代羟基二苯基化合物的制备方法
    • US06706930B2
    • 2004-03-16
    • US10275022
    • 2002-10-31
    • Armando Di TeodoroWerner HölzlDieter ReinehrRudolf Zink
    • Armando Di TeodoroWerner HölzlDieter ReinehrRudolf Zink
    • C07C4100
    • C07C45/46C07C41/26C07C45/71C07C49/807C07C49/84C07C43/295
    • There is described a process for the preparation of halogenated hydroxydiphenyl compounds of formula (1) by acylation of a halogenated benzene compound (first stage), etherification of the acylated compound with a halogenated phenol compound, which is not further substituted in the ortho-position (second stage), oxidation of the etherified compound (third stage) and hydrolysis of the oxidized compound in a fourth stage, wherein the reaction of the second stage is carried out in the presence of K2CO3 and any desired copper catalyst, where K2CO3 is used in a concentration of from 0.5 to 30 mol, based on the phenol compound employed of formula (6), according to the reaction scheme (I) in which R1 and R2 independently of one another are F, Cl or Br; R3 and R4 independently of one another are hydrogen; or C1-C4alkyl; m is 1 to 3; and n is 1 or 2. The compounds of formula (1) are used for protecting organic materials and articles from microorganisms.
    • 描述了通过酰化卤化苯化合物(第一阶段)制备式(1)的卤代羟基二苯基化合物的方法,酰化化合物与卤代酚化合物的醚化,其在邻位未被进一步取代 (第二阶段),醚化化合物的氧化(第三阶段)和氧化化合物在第四阶段的水解,其中第二阶段的反应在K 2 CO 3和任何所需的铜催化剂存在下进行,其中使用K 2 CO 3 根据反应式(I),其中R 1和R 2彼此独立地为F,Cl或Br,其浓度为0.5至30mol,基于式(6)所用的酚化合物; R 3和R 4彼此独立地是氢; 或C 1 -C 4烷基; m为1〜3; 并且n为1或2.式(1)化合物用于保护有机材料和制品免受微生物侵害。