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    • 75. 发明申请
    • Process For Producing N,N'-Carbonyldiimidazole
    • 制备N,N'-羰基二咪唑的方法
    • US20090088575A1
    • 2009-04-02
    • US11547524
    • 2005-03-29
    • Yoshikazu AokiNorimasa YokoyamaMasateru Yasumura
    • Yoshikazu AokiNorimasa YokoyamaMasateru Yasumura
    • C07D403/06
    • C07D233/54Y02P20/582
    • The present invention provides a process for producing N,N′-carbonyldiimidazole, comprising: reacting phosgene, diphosgene, or triphosgene with imidazole in an inert solvent to produce N,N′-carbonyldiimidazole; to imidazole hydrochloride yielded as a by-product in the above step, adding a gaseous or liquid basic compound represented by the below-shown general formula (1) in an inert solvent to conduct neutralization reaction; and circulating the imidazole thus generated to use it as a starting material for N,N′-carbonyldiimidazole production.In the general formula (1), R1, R2, and R3 each independently represents a hydrogen atom, a methyl group, or an ethyl group. The CDI produced by the production process of the invention is a compound useful in the fields of synthesis of pharmaceutical agents, synthesis of agricultural chemicals, peptide synthesis, and the like, e.g., intermolecular condensation reactions, intramolecular condensation reactions for synthesizing N-carboxylic anhydrides, production of activated esters, and the like. The compound is especially suitable for use in applications where colorlessness is required.
    • 本发明提供了制备N,N'-羰基二咪唑的方法,其包括:将光气,二光气或三光气与咪唑在惰性溶剂中反应以产生N,N'-羰基二咪唑; 在上述步骤中作为副产物产生的咪唑盐酸盐,在惰性溶剂中加入由下述通式(1)表示的气态或液态碱性化合物进行中和反应; 并使由此产生的咪唑循环使用其作为N,N'-羰基二咪唑生产的起始原料。 在通式(1)中,R 1,R 2和R 3各自独立地表示氢原子,甲基或乙基。 通过本发明的制造方法制备的CDI是可用于药物合成,农药合成,肽合成等领域的化合物,例如分子间缩合反应,用于合成N-羧酸酐的分子内缩合反应 ,活性酯的制备等。 该化合物特别适用于需要无色性的应用。