Synthesis of ribonucleosides of 4(5)-cyano-5(4)-methylimidazole and related 4-substituted-5-methylimidazole ribosides
作者:J. Ignacio Andrés、M. Teresa García-Lopez
DOI:10.1002/jhet.5570230308
日期:1986.5
methanolic ammonia, ammonium chloride in liquid ammonia and potassium hydrosulfide provided 4-cyano-1-β-D-ribofuranosyl-5-methylimidazole (6), 1-β-D-ribofuranosyl-5-methylimidazole-4-carboxamide (2) and 1-β-D-ribofuranosyl-5-methylimidazole-4-thiocarboxamide (11) respectively. Reaction of 6 with hydroxylamine afforded the corresponding 4-carboxamidoxime substituted nucleoside (13) which on catalytic reduction
获得了4-氰基-1-(2,3,5-三-O-乙酰基-β-D-呋喃呋喃糖基)-5-甲基咪唑(4)及其相应的5-氰基-4-甲基取代的异构体(5)通过氰化汞法对4(5)-氰基5(4)-甲基咪唑(3)进行核糖基化或3的三甲基甲硅烷基衍生物的核糖基化。用甲醇氨,液氨中的氯化铵和氢硫化钾处理4得到4-氰基-1-β-D-呋喃呋喃糖基-5-甲基咪唑(6),1-β-D-呋喃呋喃糖基-5-甲基咪唑-4-羧酰胺(2)和1-β-D-呋喃呋喃糖基-5-甲基咪唑-4-硫代羧酰胺(11) 分别。的反应6与羟胺,得到相应的4- carboxamidoxime取代的核苷(13),其上在氯化铵的存在下催化还原,被转化成1-β-d-D-呋喃核糖基-5-甲基咪唑-4-甲脒(14),为盐酸盐盐。