14C-labeled chlorogenic acid (specijic activity 30.6 nCilmg) was synthesized by reaction of diphenylmethyl-I-0-ethoxy-carbonyl- 4,5-0-isopropylidenequinate ( V ) with 0,O-dimethylcarbonyl caffeoyl chloride-u-14C (VIII) followed by selective hydrolysis of the protecting groups.
Microscale synthesis of volatile, 14C-labelled acid chlorides
β Scribed by Howard Parnes; Steve De Keczer
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- French
- Weight
- 195 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
β¦ Synopsis
A method for the microscale (one m o l e ) synthesis of volatile, 14C-labelled acid chlorides from Ba14C03 using vacuum line techniques is described. By a judicious choice of reagents, desired intermediates and products may be isolated in high yield by simple vacuum transfer techniques without fractionation.
π SIMILAR VOLUMES
14C-Labelled satigrel, or 4-cyano-5-(4'-methoxy tring-U-14CI phenyl)-5-(4"methoxyphenyl)-4-pentenoic acid was synthesized for drug metabolism and pharmacokinetic studies using 4,4'-diniethoxy [ring-U-W ] benzophenone as the starting material. The radiochemical yield was 10.0%. The specific radioacti
The synthesis of 14C-labelled crotamiton, which is a fungicide, an insecticide as well as a scabicide is described. Starting from 2-bromonitrobenzene and Cu14CN, 2-toluidine, labelled with 14C at the methyl group was prepared by the following sequence of reactions : N O ~-C ~H L + -~~C O O H
## Abstract [^14^C]Aminoguanidine was synthesized by the reaction of hydrazine sulphate with barium [^14^C]cyanamide in a oneβstep synthesis, and conveniently isolated by crystallization as the bicarbonate salt. The yield was 32%.