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    • 42. 发明授权
    • Pyrylium salts
    • 吡喃鎓盐
    • US4476313A
    • 1984-10-09
    • US494392
    • 1983-05-13
    • Kevin T. Potts
    • Kevin T. Potts
    • C07D213/22C07D213/50C07D213/70C07D215/36C07D309/34C07D311/30C07D333/22C07D333/28C07D335/02C07D405/14C07D409/06C07D409/14
    • C07D213/22C07C323/00C07D213/50C07D213/70C07D215/36C07D309/34C07D311/30C07D333/22C07D333/28C07D335/02C07D405/14C07D409/06C07D409/14
    • A method is disclosed for preparing pyrylium and thiapyrylium salts having the formula represented below (where X is O,S or Se): ##STR1## and where R.sup.1 and R.sup.2 represents a branched or unbranched alkyl radical having up to about 15 carbon atoms, an aromatic group having as substituents alkyl radicals with 1 to about 15 carbon atoms, alkoxy radicals having 1 to about 4 carbon atoms, substituted amino radicals have 1 to 2 carbon radicals containing 1 to about 4 carbon atoms, an heterocyclic group having as substitute alkyl radicals with 1 to about 15 carbon atoms, alkoxy radicals having 1 to about 4 carbon atoms and amino radicals having 1 or 2 carbon radicals containing 1 to about 4 carbons, thiophene radicals and furan radical containing a variety of substituents; R.sup.3 represents a thioalkyl radical having 1 to about 4 carbon atoms thiobenzyl, thioaryl and thiocycloalkyl, as well as thiohetaryl radicals such as thiohydridyl and related 5-and-membered systems; and Z.sup.- is an anionic function. The salts are prepared by condensing the methyl ketone with carbon disulfide in the presence of sodium hydride, treating the product with methyl iodide to form the .alpha.-oxoketenedithioacetal; condensing the .alpha.-oxoketenedithioacetal with another methyl ketone in the presence of two equivalents of potassium tert-butoxide to form a 1,5-enedione; and cyclizing the enedione with tetrafluoroboric acid.
    • 公开了一种制备具有下式(其中X为O,S或Se)的吡喃鎓和硫代吡喃鎓盐的方法:其中R 1和R 2表示具有至多约15个碳原子的支链或非支链烷基, 作为具有1至约15个碳原子的取代基的烷基的芳族基团,具有1至约4个碳原子的烷氧基,取代的氨基具有1至2个含有1至约4个碳原子的碳基,具有作为替代烷基的杂环基 具有1至约15个碳原子,具有1至约4个碳原子的烷氧基和具有1至约4个碳的1或2个碳基的氨基,包含各种取代基的噻吩基和呋喃基; R3表示具有1至约4个碳原子的硫代烷基硫代苄基,硫代芳基和硫代环烷基,以及硫代芳基如硫代氢化基和相关的5-元系体系; Z-是阴离子官能团。 盐在氢化钠存在下将甲基酮与二硫化碳缩合制备,用甲基碘处理产物以形成α-酮酮二硫缩醛; 在二当量的叔丁醇钾存在下,将α-氧基酮二硫缩醛与另一种甲基酮缩合形成1,5-烯二酮; 并用四氟硼酸环化烯酮。
    • 43. 发明授权
    • Substituted 2,2'-bipyridyl compounds and process for preparing same
    • 取代的2,2'-联吡啶化合物及其制备方法
    • US4177349A
    • 1979-12-04
    • US928396
    • 1978-07-27
    • Charles K. McGill
    • Charles K. McGill
    • C07D213/22C07D213/73
    • C07D213/22C07D213/73
    • A process for preparing substituted 2,2'-bipyridyl compounds and several compounds so prepared, the process comprising the steps of first selecting a substituted pyridine of the formula defined herein, then mixing a stoichiometric excess of the substituted pyridine with an amount of sodamide, causing the resultant mixture to be at a temperature sufficiently high to cause substituted 2,2'-bipyridyl formation, and isolating the substituted 2,2'-bipyridyl thereby formed. The new substituted 2,2'-bipyridyl compounds are selected from the group consisting of 4,4'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(cyclohexylmethyl)-2,2'-bipyridyl; 5,5'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-phenylpropyl)-2,2'-bipyridyl; 4,4'-di-(4-tetrahydropyranyl)-2,2'-bipyridyl; 4,4'-di-benzyl-2,2'-bipyridyl; 6,6'-di-isoamyl-2,2'-bipyridyl; and 4,4'-di-(t-butyl)-2,2'-bipyridyl.
    • 制备取代的2,2'-联吡啶化合物和如此制备的若干化合物的方法,该方法包括以下步骤:首先选择本文定义的式的取代吡啶,然后将化学计量过量的取代的吡啶与一定量的聚丁二酰胺混合, 使得所得混合物的温度足够高以引起取代的2,2'-联吡啶形成,并分离由此形成的取代的2,2'-联吡啶。 新的取代的2,2'-联吡啶化合物选自4,4'-二(5-壬基)-2,2'-联吡啶基; 4,4'-二(3-戊基)-2,2'-联吡啶; 6,6'-二(3-戊基)-2,2'-联吡啶; 6,6'-二(5-壬基)-2,2'-联吡啶; 4,4'-二(环己基甲基)-2,2'-联吡啶; 5,5'-二(5-壬基)-2,2'-联吡啶基; 4,4'-二(3-苯基丙基)-2,2'-联吡啶; 4,4'-二(4-四氢吡喃基)-2,2'-联吡啶; 4,4'-二苄基-2,2'-联吡啶; 6,6'-二 - 异戊基-2,2'-联吡啶; 和4,4'-二 - (叔丁基)-2,2'-联吡啶。