会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 42. 发明专利
    • Indium trisalkylacetoacetate and its preparation
    • 硝酸三乙酯及其制备
    • JPS61118338A
    • 1986-06-05
    • JP23859384
    • 1984-11-14
    • Alps Electric Co LtdKawaken Fine Chem Co Ltd
    • TORIGOE TSUNEMITSUKANO MITSURUKATO YOSHINORI
    • H01B5/14C07C49/92C07F5/00
    • NEW MATERIAL:Indium trisalkylacetoacetate of formula I (R is 2W4C alkyl).
      EXAMPLE: Indium trisethylacetoacetate.
      USE: It has stability and solubility in an organic solvent, and is useful for forming an electrically conductive transparent coating film. It can be applied easily by screen-pinting. Since the compound is soluble in organic solvent, a paste having high concentration can be prepared easily. The paste is suitable espe cially for forming an electrically conductive transparent coating film for liquid crystal display element.
      PREPARATION: The compound of formula I can be prepared by reacting 1 mol of indium triisopropylate of formula II with preferably 3 mol of alkyl acetoacetate of formula III in a solvent such as benzene at ≥100°C.
      COPYRIGHT: (C)1986,JPO&Japio
    • 新材料:式I的三烷基乙酰乙酸铟(R为2-4C烷基)。 实施例:三乙酰乙酸铟。 用途:在有机溶剂中具有稳定性和溶解性,可用于形成导电性透明涂膜。 它可以轻松应用于丝印。 由于化合物可溶于有机溶剂,因此可以容易地制备高浓度的糊剂。 该浆料特别适用于形成用于液晶显示元件的导电透明涂膜。 制备:式I化合物可以通过使1摩尔式II的三异丙醇铟与优选3摩尔的式III的乙酰乙酸烷基酯在溶剂如苯中在> = 100℃下反应来制备。
    • 43. 发明专利
    • Perfumery composition
    • 造纸组合物
    • JPS59204115A
    • 1984-11-19
    • JP7879683
    • 1983-05-04
    • Kao CorpKawaken Fine Chem Co Ltd
    • FUKUDA SHIGEOSATOU TAKAMINAKAJIMA MOTOKI
    • A61K8/33A61Q13/00C11B9/00
    • PURPOSE: To provide a perfumery composition containing 3- and/or 2-(cyclohex-3- enyl)propanal, having refreshing green note and exhibiting sweet and mild fragrance when compounded with conventional compounded perfume.
      CONSTITUTION: A perfumery composition containing 0.01W10wt% of the compound of formula I (R is group of formula II or formula III). Although the compound of formula I exhibits strong unagreeable odor as it is, however, the compound of formula I wherein R is group of formula II exhibits leafy green fruity fragrance and the compound of formula I wherein R is group of formula III exhibits green spicy woody fragrance in an extremely dilute state. These compounds can be used, without being separated from each other, in the form of a mixture as a perfume for soap, detergent, cosmetic, etc.
      COPYRIGHT: (C)1984,JPO&Japio
    • 目的:提供含有3-和/或2-(环己-3-烯基)丙醛的香料组合物,当与常规复合香料混合时,具有清爽的绿色音符并呈现甜而温和的香味。 构成:含有0.01-10wt%式I化合物(R为式II或式III基团)的香料组合物。 尽管式I的化合物表现出强烈的不可原谅的气味,但是其中R为式II基团的式I化合物显示出绿叶绿色水果香料,其中R为式III基团的式I化合物显示出绿色木香 香味极度稀薄。 这些化合物可以不以彼此分离的形式用作香皂,洗涤剂,化妆品等作为混合物的形式使用。
    • 44. 发明专利
    • Preparation of omega-indol-3-yl-alkanol compound
    • OMEGA-INDOL-3-YL-ALKANOL化合物的制备
    • JPS58192867A
    • 1983-11-10
    • JP7450082
    • 1982-05-06
    • Kawaken Fine Chem Co Ltd
    • TAKANASHI KOUJIKUBO MASAAKI
    • C07D209/12
    • PURPOSE: To prepare the titled compound, in high yield, by reacting a phenylhydrazine compound with a specific amount of an oxacycloalkan-2-ol compound in the presence of the necessary amount of a strong acid to convert the mixture to hydrochloride.
      CONSTITUTION: The objective compound of formula VI is prepared by reacting (A) 1mol of a phenylhydrazine compound of formula I (R
      1 is H, lower alkyl, aryl, or aralkyl; R
      2 is R
      1 , lower alkoxy, aryloxy, aralkoxy, or halogen) with (B) 1.1W 3mol of one or more oxacycloalkan-2-ol compounds of formula II [R
      3 is H or lower alkyl; R
      4 is group of formula III (R
      7 is H or lower alkyl; k is 0W2) or formula IV; R
      5 is lower alkyl; n is 0 or 1] or formula V (R
      6 is H or CH
      3 ; l is 1 or 2), in a solvent containing one or more alcoholic compounds in the presence of a specific amount of a strong acid at 70W170°C for 30minW several hours.
      USE: Raw material indole derivatives, etc.
      COPYRIGHT: (C)1983,JPO&Japio
    • 目的:为了以高产率制备标题化合物,通过使苯肼化合物与特定量的氧杂环烷-2-醇化合物在必要量的强酸存在下反应,将混合物转化成盐酸盐。 结构式:式Ⅵ的目标化合物是通过使(A)1摩尔式I的苯肼化合物(R 1为H,低级烷基,芳基或芳烷基; R 2为R 1,低级烷氧基,芳氧基,芳烷氧基或卤素) 与(B)1.1-3mol的一种或多种式Ⅱ的氧杂环烷-2-醇化合物[R3是H或低级烷基; R4是式III的基团(R7是H或低级烷基; k是0-2)或式IV; R5是低级烷基; 在特定量的强酸存在下,在70-170℃下,在含有一种或多种醇化合物的溶剂中,n为0或1]或式V(R 6为H或CH 3; l为1或2) 30分钟 - 数小时。 用途:原料吲哚衍生物等
    • 45. 发明专利
    • Preparation of nicotinic acid derivative
    • 非酸性衍生物的制备
    • JPS57126478A
    • 1982-08-06
    • JP1119581
    • 1981-01-27
    • Kawaken Fine Chem Co Ltd
    • KAWAMOTO AKIRAYASAKA SHIYOUTA
    • C07D309/36C07D213/80C07D213/803C07D309/38
    • PURPOSE: To obtain 6-hydroxy-6-methylnicotinic acid advantageously, by reacting an N-N'-bis(6-methyl-4-oxo-3,4-dihydro-2-pyrrone-3-indenemethyl) alkylenediamide with ammonia.
      CONSTITUTION: Preferably 1mol compound shown by the formulaI(R
      1 and R
      2 are H, 1W3C alkyl, aryl; n is 2W3), e.g., N,N'-bis (6-methyl-4-oxo-3,4-dihydro-2- pyrrone-3-indenemethyl)ethylenediamine is reacted with 2W4mol ammonia using a solvent such as methoxyethanol in a sealed tube or in an autoclave at 80W 120°C, to give a compound shown by the formula II useful as an intermedate for drugs such as a cephalosporin derivative, etc. from industrially easily obtainable raw materials by one step without using expensive raw materials such as N,N'- dimethylformamide methylacetal, etc.
      COPYRIGHT: (C)1982,JPO&Japio
    • 目的:有利地通过使N-N'-双(6-甲基-4-氧代-3,4-二氢-2-吡咯烷-3-茚基甲基)亚烷基二胺与氨反应获得6-羟基-6-甲基烟酸。 构成:优选1摩尔化合物由式I表示(R1和R2是H,1-3C烷基,芳基; n是2-3),例如N,N'-双(6-甲基-4-氧代-3,4- - 二氢-2-吡咯烷-3-茚基甲基)乙二胺在密封管中或在80-120℃的高压釜中使用溶剂如甲氧基乙醇与2-4mol氨反应,得到式II所示的化合物 可用作工业上容易获得的原料等药物如头孢菌素衍生物的一个步骤,而不使用昂贵的原料如N,N'-二甲基甲酰胺甲缩醛等。
    • 46. 发明专利
    • Preparation of 2-aminopropanol derivative
    • 2-氨基丙醇衍生物的制备
    • JPS57126451A
    • 1982-08-06
    • JP1195781
    • 1981-01-29
    • Kawaken Fine Chem Co Ltd
    • NOZUE MORIAKIYANAGISAWA KUNIMICHI
    • C07B61/00B01J23/00B01J23/42C07C67/00C07C213/00C07C215/30C07C217/70
    • Y02P20/52
    • PURPOSE: To prepare the titled compound useful as a medicine for the circulatory organs, etx., economically and safely, by the catalytic reduction of a 2-hydroxyiminopropiophenone derivative in an organic solvent containing hydrochloric acid in the presence of a platinum-carbon catalyst.
      CONSTITUTION: The 1-pheny1-2-aminopropanol derivative of formula II (X is methyl, methoxy, OH or halogen) is prepared by the catalytic reduction of the compound of formulaIin an organic solvent containing hydrochloric acid in the prosence of a platinum-carbon catalyst. The amount of hydrochloric acid is 1W6mol, pref. 2W5mol/1mol of the starting compound. The solvent is pref. methanol, ethanol, etc. Since hydrogen chloride gas is not used in the reaction, the objective compound can be obtained safely, in high selectivity, with little side reactions. The compound of formula II is also useful as a drug acting to the sympathetic nervous system.
      COPYRIGHT: (C)1982,JPO&Japio
    • 目的:通过在铂 - 碳催化剂存在下,通过在含有盐酸的有机溶剂中催化还原2-羟基亚氨基苯基酮衍生物,制备用作循环器官药物的标题化合物,经济,安全。 构成:式Ⅱ的1-苯基-2-氨基丙醇衍生物(X是甲基,甲氧基,OH或卤素)是通过在含有盐酸的有机溶剂中催化还原式I化合物来制备的, 催化剂。 盐酸的量为1-6mol, 2-5mol / 1mol起始化合物。 溶剂优先。 甲醇,乙醇等。由于反应中不使用氯化氢气体,所以可以安全,高选择性,少量副反应得到目标化合物。 式II化合物也可用作作用于交感神经系统的药物。
    • 47. 发明专利
    • Preparation of 1,3-dialkyl-2-imidazolidinone
    • 1,3-二烷基-2-咪唑啉酮的制备
    • JPS57120570A
    • 1982-07-27
    • JP747281
    • 1981-01-21
    • Kawaken Fine Chem Co Ltd
    • ITOU KAZUHISATAKANO SUSUMUYASAKA SHIYOUTAISHII MUTSUO
    • C07D233/34
    • PURPOSE: To prepare 1,3-dialkyl-2-imidazolidinone useful as an intermediate raw material in organic synthetic chemistry, a phase-transfer catalyst, etc., easily, in high yield, by reacting 1,2-dichloroethane with an alkylamine, and then reacting the product with CO
      2 .
      CONSTITUTION: 1,2-Dichloroethane is made to react with an alkylamine of formula RNH
      2 (R is 1W3C alkyl) to obtain N,N'-alkylethylenediamine of formula II. After removing the by-products from the reaction mixture, or isolating and purifying the compound of formula II, the reaction product is made to react with solid or gaseous CO
      2 to afford the objective 1,3-dialkyl-2-imidazolidinone of formulaI.
      COPYRIGHT: (C)1982,JPO&Japio
    • 目的:通过使1,2-二氯乙烷与烷基胺反应,可以容易地以高产率制备有机合成化学中有用的中间原料的1,3-二烷基-2-咪唑烷酮,相转移催化剂等, 然后使产物与二氧化碳反应。 构成:使1,2-二氯乙烷与式RNH2(R为1-3C烷基)的烷基胺反应,得到式II的N,N'-烷基乙二胺。 在从反应混合物中除去副产物或分离和纯化式II化合物后,使反应产物与固体或气态CO 2反应,得到式I的目的1,3-二烷基-2-咪唑啉酮。
    • 48. 发明专利
    • Preparation of n,n'-dialkylethylenediamine
    • N,N'-二烷基乙烯基胺的制备
    • JPS57120552A
    • 1982-07-27
    • JP747381
    • 1981-01-21
    • Kawaken Fine Chem Co Ltd
    • TAKANO SUSUMUITOU KAZUHISAYASAKA SHIYOUTAISHII MUTSUO
    • C07B61/00B01J21/00B01J23/00B01J23/56B01J25/00C07C67/00C07C209/00C07C209/26C07C211/10
    • Y02P20/52
    • PURPOSE: To prepare the titled compound useful as an intermediate raw material in organic synthetic chemistry, economically, in an industrial scale, without troubles of apparatus corrosion nor necessitating high temperature and pressure, by reacting glyoxal with an alkylamine in the presence of H and a hydrogenation catalyst.
      CONSTITUTION: Glyoxal, an alkylamine (primary amine having 1W6C alkyl), a solvent such as water, and a hydrogenation catalyst (e.g. a platinum-group catalyst) are charged in an autoclave, the autoclave is sealed and substituted sufficiently with hydrogen, and the reactants are subjected to the catalytic amination reaction under normal or positive pressure. After the completion of the reaction, the content is cooled, the catalyst is separated, and the product is distilled under normal or reduced pressure to obtain the titled compound. The reaction temperature is pref. as low as possible, i.e. between normal temp. and 100°C. The reaction temperature of >100°C is undesirable because the polycondensation of the reaction products takes place. The hydrogen pressure is pref. 10W200kg/cm
      2 .
      COPYRIGHT: (C)1982,JPO&Japio
    • 目的:为了在有机合成化学中有效地制备作为中间原料的标题化合物,在经济上,在工业规模上,没有设备腐蚀的问题,也不需要高温和高压,通过乙二醛与烷基胺在H和 氢化催化剂。 构成:在高压釜中加入乙二醛,烷基胺(具有1-6C烷基的伯胺),溶剂如水和氢化催化剂(例如铂族催化剂),将高压釜密封并充分用氢气置换, 并在正常或正压下使反应物进行催化胺化反应。 反应完成后,将内容物冷却,分离催化剂,在正常或减压下蒸馏产物,得到标题化合物。 反应温度为最佳。 尽可能低,即在正常温度之间。 和100℃ 反应温度> 100℃是不合需要的,因为反应产物的缩聚发生。 氢气压力是最好的。 10-200kg / cm 2。
    • 49. 发明专利
    • Novel 1-(3'-aminopropyl)tetrahydro-beta-carboline compound and its preparation
    • 新型1- 3'-氨基丙酸四氢 - 碳 - 碳化合物及其制备方法
    • JPS5728087A
    • 1982-02-15
    • JP10305580
    • 1980-07-29
    • Kawaken Fine Chem Co Ltd
    • KUBO MASAAKIFUKUDA SHIGEOSASAKI TAKASHI
    • C07D471/04
    • NEW MATERIAL:A 1-(3'-aminopropyl)tetrahydro-β-carboline compound shown by the formula I [R is H, 1W6C alkyl, etc.; R
      1 is H, 1W6C alkyl, etc.; R
      2 and R
      3 are as shown for R
      1 , R
      5 CO-(R
      5 is 1W6C alkyl, etc.); R
      4 is H or 1W6C alkyl; group shown by the formula II may be group shown by the formula III (n is 1W3, m is 2 or 3; X is -CH
      2 -, O, etc.); when R
      3 is R
      5 CO- and the sum of the alkyl carbon of R
      4 and R
      5 is 4W8, R
      4 and R
      5 may be subjected to ring closure to form group shown by the formula IV (l is 4W8)].
      EXAMPLE: 1-(3'-Aminopropyl)tetrahydro-β-carboline.
      USE: An intermediate for synthesizing a drug, agricultural chemical, and indole alkaloid.
      PROCESS: A tryptamine compound shown by the formula V is reacted with a compound shown by the formula VI (R
      5 and R
      6 are 1W4C alkyl, etc.) in water and/or hydrophilic solvent at 60W140°C while the reaction solution being kept acidic, to give a compound shown by the formula I.
      COPYRIGHT: (C)1982,JPO&Japio
    • 新材料:式I所示的1-(3'-氨基丙基)四氢-β-咔啉化合物[R是H,1-6C烷基等; R 1是H,1-6C烷基等; R 2和R 3如R 1所示,R 5 CO-(R 5是1-6 C烷基等); R 4是H或1-6C烷基; 式II所示的基团可以是式III所示的基团(n为1-3,m为2或3; X为-CH 2 - ,O等); 当R 3为R 5 CO-且R 4和R 5的烷基碳之和为4-8时,R 4和R 5可以进行环封合 式(IV)表示的化合物(I为4-8)]。 实施例:1-(3'-氨基丙基)四氢-β-咔啉。 用途:合成药物,农药和吲哚生物碱的中间体。 方法:将式V所示的色胺化合物与式VI中所示的化合物(R 5和R 6为1-4 C烷基等)在水和/或亲水溶剂中在60-140℃下反应 同时使反应溶液保持酸性,得到式I所示的化合物。