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5-FLUORO-5,6-DIHYDROURACIL DERIVATIVE

机译:5-氟-5,6-二氢尿嘧啶衍生物

摘要

NEW MATERIAL:The compound of formula I [X is halogen; Y is -NR2- (R2 is H or lower alkyl) or -O-; Z is lower alkylene; l is 0 or 1; R1 is carboxyl, lower alkoxycarbonyl or group of formula II (R3 is cyano; R4 is benzoyloxy, etc.)]. EXAMPLE:dl-5-Bromo-6-(4-carboxy-N-methylanilino)-5-fluoro-5,6-dihydrou racil. USE:A carcinostatic agent. PREPARATION:The compound of formula I can be produced e.g. by reacting a compound of formula III (R5 is lower alkanoyl) with a compound of formula IV in an inert solvent (e.g. ketone, ether, aromatic hydrocarbon, etc.) in the presence of an acid acceptor (e.g. potassium carbonate, pyridine, etc.) at room temperature-80 deg.C for 1-24hr.
机译:新材料:式I的化合物[X为卤素; Y为-NR 2-(R 2为H或低级烷基)或-O-; Z为低级亚烷基; l是0或1; R 1为羧基,低级烷氧羰基或式II的基团(R 3为氰基; R 4为苯甲酰氧基等)]。实施例:dl-5-溴-6-(4-羧基-N-甲基苯胺基)-5-氟-5,6-二氢尿嘧啶。用途:抗癌剂。制备:可以制备例如式I的化合物。在酸性受体(例如碳酸钾)的存在下,在惰性溶剂(例如酮,醚,芳烃等)中,使式III化合物(R 5为低级烷酰基)与式IV化合物反应吡啶等)在室温-80摄氏度下放置1-24小时。

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