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    • 1. 发明专利
    • Method for producing 5-aryl-3-amino-2-alkoxycarbonylthiophene compound
    • 5-亚氨基-3-氨基-2-烷氧羰基二苯醚化合物的制备方法
    • JP2011168556A
    • 2011-09-01
    • JP2010035627
    • 2010-02-22
    • Sumitomo Seika Chem Co Ltd住友精化株式会社
    • FUJITA KOJISATAKE SHUZOASHIKAWA MASAYASUFUKADA KANAKO
    • C07D333/40
    • PROBLEM TO BE SOLVED: To provide a method for simply producing a 5-aryl-3-amino-2-alkoxycarbonylthiophene compound useful as a medicine, etc., in a high yield.
      SOLUTION: The method for producing a 5-aryl-3-amino-2-alkoxycarbonylthiophene compound represented by formula (4) (wherein R
      1 is a hydrogen atom, halogen atom, 1C-4C alkyl, 1C-4C alkoxy, nitro or trifluoromethyl; R
      2 is a hydrogen atom or 1C-4C alkyl) includes reacting an acetophenone compound which may be substituted or not with a halogen atom, a 1C-4C alkyl group, a 1C-4C alkoxy group, a nitro group or a trifluoromethyl group with an N-substituted formamide, a chlorinating agent and a hydroxylamine compound to give a 3-chloro-3-arylacrylonitrile compound containing an aryl group which may be substituted or not as the above, continuously, reacting the resultant compound with thioglycolic acid or a thioglycolic acid ester compound in the presence of a base.
      COPYRIGHT: (C)2011,JPO&INPIT
    • 待解决的问题:提供以高产率简单地制备用作药物等的5-芳基-3-氨基-2-烷氧基羰基噻吩化合物的方法。 解决方案:制备由式(4)表示的5-芳基-3-氨基-2-烷氧基羰基噻吩化合物的方法(其中R 1 是氢原子,卤素原子,1C-4C 烷基,1C-4C烷氧基,硝基或三氟甲基; R 2是氢原子或1C-4C烷基)包括使可被取代或不与卤素原子取代的苯乙酮化合物,1C-4C 烷基,1C-4C烷氧基,硝基或三氟甲基与N-取代甲酰胺,氯化剂和羟胺化合物反应,得到含有可被取代的芳基的3-氯-3-芳基丙烯腈化合物 或不如上所述,在碱的存在下,使所得化合物与巯基乙酸或巯基乙酸酯化合物反应。 版权所有(C)2011,JPO&INPIT
    • 6. 发明专利
    • (e)-n-monoalkyl-3-oxo-3-(2-thienyl)propenamine and method for manufacturing the same as well as method for manufacturing (e, z)-n-monoalkyl-3-oxo-3-(2-thienyl) propenamine
    • (E)-N-单甲基-3-氧代-3-(2-噻吩基)丙炔及其制备方法以及制备(E,Z)-N-单甲基-3-氧代-3-(2 -THIENYL)PROPENAMINE
    • JP2013256501A
    • 2013-12-26
    • JP2013146139
    • 2013-07-12
    • Sumitomo Seika Chem Co Ltd住友精化株式会社
    • SATAKE SHUZOHAYASHISAKA TOKUYUKIFUSHIYA ICHIROTANAKA MUNEAKIKAGANO HIROKAZU
    • C07D333/22
    • C07D333/22
    • PROBLEM TO BE SOLVED: To provide an (E)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine expressed by formula (1) that is used in a method for manufacturing with ease and in a high yield an (E, Z)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine.SOLUTION: An (E)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine expressed by formula (1) is manufactured in such a way that a solution in which (Z)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine is dissolved in a solvent, is kept at a temperature of 25°C or below to crystallize and from the deposited crystals the crystals with a particle diameter of 100 μm or less are fractionated. (E, Z)-N-monoalkyl-3-oxo-3-(2-thienyl)propenamine is manufactured in such a way that a reaction liquid which is obtained by the reaction of an alkali metal salt of β-oxo-β-(2-thienyl)propanal with a monoalkylamine compound is added with a water-insoluble organic solvent to liquid-separate into an organic layer, to which seed crystals containing the compound expressed by formula (1) are added and kept at a temperature of 25°C or below (In the formula, R is a 1-4C alkyl group.).
    • 要解决的问题:提供一种用于制备方法的式(1)表示的(E)-N-单烷基-3-氧代-3-(2-噻吩基)丙烯胺,并且以高产率a (E,Z)-N-单烷基-3-氧代-3-(2-噻吩基)丙烯胺。溶液:由式((E,Z)-N-单烷基-3-氧代-3- 1)以使(Z)-N-单烷基-3-氧代-3-(2-噻吩基)丙烯胺溶解在溶剂中的溶液的温度保持在25℃以下的温度 从析出的结晶中析出粒径为100μm以下的晶体。 (E,Z)-N-单烷基-3-氧代-3-(2-噻吩基)丙烯胺的制备方法是使通过碱金属盐与氧化反应生成的反应液 加入具有单烷基胺化合物的(2-噻吩基)丙醛与水不溶性有机溶剂一起液体分离成有机层,加入含有式(1)表示的化合物的晶种并保持在其中 为25℃以下(式中,R为1-4C烷基)。
    • 8. 发明专利
    • Method for producing nitrothiophenol
    • 生产硝基苯酚的方法
    • JP2012051842A
    • 2012-03-15
    • JP2010196243
    • 2010-09-01
    • Sumitomo Seika Chem Co Ltd住友精化株式会社
    • FUJITA KOJISATAKE SHUZOASHIKAWA MASAYASU
    • C07C319/28C07C319/06C07C323/09
    • PROBLEM TO BE SOLVED: To provide a method for producing a nitrothiophenol, by which the nitrothiophenol can be obtained in high purity.SOLUTION: The method for producing the nitrothiophenol comprises a nitrothiophenol production process and a purification process. The nitrothiophenol production process comprises hydrolyzing a specific halomethylthionitrobenzene to obtain a mixture containing the nitrothiophenol. The purification process comprises treating the mixture with an alkali compound in the presence of the aqueous solution of the alkali compound and a hydrophobic organic solvent, separating the water phase from the organic solvent phase, and then treating the water phase with an acid compound in the presence of an aqueous solution of the acid compound and the hydrophobic organic solvent to isolate the nitrothiophenol from the mixture, thereby purifying.
    • 待解决的问题:提供硝基苯硫酚的制备方法,通过该方法可以获得高纯度的硝基苯硫酚。 解决方案:硝基苯硫酚的制备方法包括硝基苯硫酚生产方法和纯化方法。 硝基苯硫酚的制备方法包括水解特定的卤代甲硫基硝基苯,得到含有硝基苯硫酚的混合物。 纯化方法包括在碱性化合物的水溶液和疏水性有机溶剂的存在下用碱性化合物处理混合物,将水相与有机溶剂相分离,然后用酸化合物处理水相 存在酸化合物和疏水性有机溶剂的水溶液以从混合物中分离出硝基苯硫酚,从而进行纯化。 版权所有(C)2012,JPO&INPIT
    • 9. 发明专利
    • Method of producing thiophene sulfonyl carbamate
    • 生产噻吩磺酸碳酸酯的方法
    • JP2012041288A
    • 2012-03-01
    • JP2010182675
    • 2010-08-18
    • Sumitomo Seika Chem Co Ltd住友精化株式会社
    • TANAKA MUNEAKISATAKE SHUZOFURUKAMI KENJIKOBAYASHI TETSUYA
    • C07D333/34
    • PROBLEM TO BE SOLVED: To provide a method of producing thiophene sulfonyl carbamate useful as an intermediate of a medicine, a pesticide or the like efficiently and by high purity.SOLUTION: The method comprises reacting thiophene sulfonamide expressed by formula (1) (wherein Xdenotes a hydrogen atom or a halogen atom), and alkyl halocarbonate expressed by X-CO-OR (wherein Xdenotes a halogen atom, and R denotes a 1-4C alkyl group) in a hydrophilic organic solvent in the presence of an alkali metal carbonate and water to produce thiophene sulfonyl carbamate expressed by formula (3) (wherein Xdenotes the same atom as that of formula (1), and R denotes a 1-4C alkyl group).
    • 待解决的问题:提供以有效和高纯度生产用作药物,农药等的中间体的噻吩磺酰基氨基甲酸酯的方法。 解决方案:该方法包括使由式(1)表示的噻吩磺酰胺(其中X 1 表示氢原子或卤素原子)和由X'表示的卤代碳酸烷基酯反应, 亲水性(其中X 2 表示卤素原子,R表示1-4C烷基) 有机溶剂在碱金属碳酸盐和水的存在下反应以制备由式(3)表示的噻吩磺酰氨基甲酸酯(其中X 1 表示与式(1)相同的原子, ,R表示1-4C烷基)。 版权所有(C)2012,JPO&INPIT