发明名称 SYNTHESIS OF AMINOLEVULINIC ACID
摘要 PURPOSE:To obtain the titled compound having physiological activity and labeled with stable isotope, easily, efficiently and selectively at a low cost in large quantities, by using a <13>C-cyanogen compound and succinyl chloride available at a relatively low cost as starting substances and treating with ultrasonic wave, etc. CONSTITUTION:A succinyl chloride compound of formula I (R is CH3 or C2H5; X is OH or Cl) and a <13>C-cyanogen compound of formula II (M is K, Na, Ag, Cu, etc.) are refluxed in a solvent such as acetonitrile in argon stream at 100 deg.C for 30min and the produced compound of formula III is mixed with a mixture of acetic acid and acetic anhydride and activated zinc powder and reduced and acetylated by applying ultrasonic wave for 5-10min. The obtained compound of formula IV is hydrolyzed with a mineral acid to quantitatively produce the objective [5-<13>C]-aminolevulinic acid hydrochloride of formula V. USE:The compound is expected to be useful as a diagnostic for congenital porphyria which is clinically genetic metabolic disease and for lead poisoning, etc., attracting public attention from the view point of labor hygienicity.
申请公布号 JPS62111954(A) 申请公布日期 1987.05.22
申请号 JP19850251070 申请日期 1985.11.09
申请人 JAPAN SPECTROSCOPIC CO 发明人 KAJIWARA MASAHIRO
分类号 A61K51/00;C07C67/00;C07C227/00;C07C227/14;C07C229/22;C09B59/00 主分类号 A61K51/00
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