A concise synthesis of [carbonyl‐11C]melatonin and N‐[carbonyl‐ 11C]acetylserotonin

Rapid chemical syntheses of [carbonyl- 11C]melatonin and N-[carbonyl- 11C]acetylserotonin starting from [11C]carbon dioxide are described. The radiochemical yield (based on [carbonyl-11C]-acetic acid), purity, and the specific activity (end of bombardment) of the former are 12%, >98%, and 4.2 Ci/μmol, respectively. The latter is also synthesized with the same radiochemical yield, purity, and specific activity. The total times required for their syntheses are ca. 45 min, respectively.

[1]  G. Slegers,et al.  Enzymatic synthesis of [11C]N-acetylserotonin , 1990 .

[2]  C. Gottfries Disturbance of the 5-hydroxytryptamine metabolism in brains from patients with Alzheimer's dementia. , 1990, Journal of neural transmission. Supplementum.

[3]  R. Reiter,et al.  Melatonin receptors: current status, facts, and hypotheses. , 1990, Life sciences.

[4]  A. Miles Melatonin: perspectives in the life sciences. , 1989, Life sciences.

[5]  K. Ishiwata,et al.  A convenient synthesis of D‐[1‐11C]glucopyranose and D‐[1‐11C]galactopyranose using diborane , 1989 .

[6]  K. Ishiwata,et al.  Comparative study of specific activity of [11C]methyl iodide: A search for the source of carrier carbon , 1988 .

[7]  S. Luthra,et al.  Radiosynthesis of NCA [carbonyl-11C]6-fluoromelatonin. , 1988, International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes.

[8]  S. Luthra,et al.  The preparation of a carbon-11 labelled neurohormone--[11C]melatonin. , 1987, International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes.