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    • 5. 发明授权
    • Synthesis, uses and compositions of crystal hydrogels
    • 水凝胶的合成,用途和组成
    • US07347988B2
    • 2008-03-25
    • US10295484
    • 2002-11-15
    • Zhibing HuXihua LuJun GaoTong CaiGang HuangBo Zhou
    • Zhibing HuXihua LuJun GaoTong CaiGang HuangBo Zhou
    • A61K7/021
    • G02B1/04C08F220/56C08J3/075G01N2021/7723
    • A method is disclosed for creating hydrogels with ordered crystalline structures that exhibit a characteristic colored opalescence. In addition to the unique optical properties, these materials contain a large amount of water in their crosslinked networks. The manufacturing processes include synthesizing monodispersed hydrogel nanoparticles containing specific reactive functional groups, self-assembly of these particles to form a crystalline structure, and subsequent crosslinking neighboring spheres to stabilize the entire network. Polymerizing a hydrogel monomeric composition around the crystalline structure can enhance the mechanical strength. The resulting network is dimensionally and thermodynamically stabile under various pH and temperature conditions. The color and volume of these crystalline hydrogel networks can reversibly change in response to external stimuli such as temperature, pH and other environmental conditions. These new materials may lead to a variety of technological and artistic applications, ranging from sensors, displays, controlled drug delivery devices, jewelry and decorative consumer products.
    • 公开了一种用于产生具有有色晶体结构的水凝胶的方法,其具有特征性的着色乳光。 除了独特的光学性能之外,这些材料在其交联网络中含有大量的水。 制造方法包括合成包含特定反应性官能团的单分散水凝胶纳米颗粒,这些颗粒的自组装形成晶体结构,随后交联相邻球体以稳定整个网络。 在晶体结构周围聚合水凝胶单体组合物可以增强机械强度。 所得到的网络在各种pH和温度条件下在尺寸和热力学上是稳定的。 这些结晶水凝胶网络的颜色和体积可以响应于诸如温度,pH和其他环境条件的外部刺激而可逆地改变。 这些新材料可能导致各种技术和艺术应用,从传感器,显示器,受控药物输送装置,首饰和装饰消费品。
    • 6. 发明申请
    • method for preparing 2-(N-substituted)-amino-benzimidazole derivatives
    • 制备2-(N-取代) - 氨基 - 苯并咪唑衍生物的方法
    • US20130345436A1
    • 2013-12-26
    • US13976865
    • 2011-01-26
    • Yueheng JiangTong CaiLimin QueZhigang Lin
    • Yueheng JiangTong CaiLimin QueZhigang Lin
    • C07D235/30
    • C07D235/30C07C273/1836C07C303/40C07D235/14Y02P20/55C07C311/21C07C275/40
    • A method for preparing 2-(N-substituted)-amino-benzimidazole derivatives is provided, which comprises the following steps: (1) reacting a compound of 2-(N-protecting group)-O-aryl diamine with a compound of N-phenoxycarbonyl monosubstituted amine to obtain a compound of 2-(N-protecting group)-amino aryl urea; (2) in a suitable organic solvent, performing dehydrating cyclization reaction of the compound of 2-(N-protecting group)-amino aryl urea in the presence of an organic base and dichloro triphenylphosphine prepared by triphenylphosphine oxide with oxalyl chloride or diphosgene or triphosgene, or dibromo triphenylphosphine prepared by triphenylphosphine oxide with bromine, to produce a compound of 1-protecting group-2-(N-substituted)-amino-benzimidazole; (3) deprotecting the resulting compound of 1-protecting group-2-(N-substituted)-amino-benzimidazole to obtain the compound 2-(N-substituted)-amino-benzimidazole.
    • 提供了制备2-(N-取代的) - 氨基 - 苯并咪唑衍生物的方法,其包括以下步骤:(1)使2-(N-保护基)-O-芳基二胺的化合物与N - 苯氧基羰基单取代胺,得到2-(N-保护基) - 氨基芳基脲的化合物; (2)在合适的有机溶剂中,在有机碱和通过三苯基氧化膦与草酰氯或双光气或三光气制备的二氯三苯基膦存在下进行2-(N-保护基) - 氨基芳基脲的化合物的脱水环化反应 或由三苯基膦氧化物与溴制备的二溴三苯基膦,得到1-保护基-2-(N-取代的) - 氨基 - 苯并咪唑的化合物; (3)将所得的1-保护基-2-(N-取代的) - 氨基 - 苯并咪唑化合物脱保护,得到化合物2-(N-取代的) - 氨基 - 苯并咪唑。
    • 8. 发明授权
    • Preparation method of high-optical purity N2-[1 -(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine
    • 高光纯度N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸的制备方法
    • US08940929B2
    • 2015-01-27
    • US13822690
    • 2010-09-29
    • Limin QueYueheng JiangZhigang LinTong Cai
    • Limin QueYueheng JiangZhigang LinTong Cai
    • C07C229/00C07C51/42C07C231/20
    • C07C51/42C07B2200/07C07C231/20C07C233/47
    • Disclosed is a preparation method of high-optical purity N2-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine. The method includes: adding crude N2-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine to one or more organic solvents, and then reacting with an organic acid to form a salt, which is precipitated, thereby achieving the purpose of separation and purification; next, adding the obtained solid or mother concentrate into deionized water, and then adding an inorganic base or an organic base for basification, so as to adjust the pH value, removing the organic acid, filtering, washing and drying, to obtain the high-optical purity N2-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine, where the molar ratio of 1S-isomer to 1R-isomer is equal to or greater than 99:1.
    • 公开了高光学纯度N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸的制备方法。 该方法包括:向一种或多种有机溶剂中加入粗N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸,然后与有机酸反应形成盐, 沉淀,从而达到分离纯化的目的; 然后,将得到的固体或母体浓缩物加入去离子水中,然后加入无机碱或有机碱进行碱化,调节pH值,除去有机酸,过滤,洗涤和干燥, 光学纯度N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸,其中1S-异构体与1R-异构体的摩尔比等于或大于99:1。
    • 10. 发明申请
    • PREPARATION METHOD OF HIGH-OPTICAL PURITY N2-[1-(S)-ETHOXYCARBONYL-3-PHENYLPROPYL]-N6-TRIFLUOROACETYL-L-LYSINE
    • 高光固化N2- [1-(S) - 乙氧羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸的制备方法
    • US20130178651A1
    • 2013-07-11
    • US13822690
    • 2010-09-29
    • Limin QueYueheng JiangZhigang LinTong Cai
    • Limin QueYueheng JiangZhigang LinTong Cai
    • C07C51/42
    • C07C51/42C07B2200/07C07C231/20C07C233/47
    • Disclosed is a preparation method of high-optical purity N2-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine. The method includes: adding crude N2-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine to one or more organic solvents, and then reacting with an organic acid to form a salt, which is precipitated, thereby achieving the purpose of separation and purification; next, adding the obtained solid or mother concentrate into deionized water, and then adding an inorganic base or an organic base for basification, so as to adjust the pH value, removing the organic acid, filtering, washing and drying, to obtain the high-optical purity N2-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-N6-trifluoroacetyl-L-lysine, where the molar ratio of 1S-isomer to 1R-isomer is equal to or greater than 99:1.
    • 公开了高光学纯度N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸的制备方法。 该方法包括:向一种或多种有机溶剂中加入粗N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸,然后与有机酸反应形成盐, 沉淀,从而达到分离纯化的目的; 然后,将得到的固体或母体浓缩物加入去离子水中,然后加入无机碱或有机碱进行碱化,调节pH值,除去有机酸,过滤,洗涤和干燥, 光学纯度N2- [1-(S) - 乙氧基羰基-3-苯基丙基] -N6-三氟乙酰基-L-赖氨酸,其中1S-异构体与1R-异构体的摩尔比等于或大于99:1。