N N , di-2 chloroethyl 4-amino 2-methyl 1-methoxy naphtalen i s labelled with C on two different positions. -uniformly on the four carbons of the dichloroethyl group by means of radioactive ethylene oxide. -o n the carbon of the methoxy group by means of radioactive methyl iodide. ## 14 RESUME L
Synthese DU N- [(ethyl - 1 pyrrolidinyl -2) methyl] methoxy-2 sulfamoyl -5 benzamide (sulpiride) marque AU 14C
✍ Scribed by J. P. Noël; A. Benakis; M. Herbert; L. Pichat; M. Thominet
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- French
- Weight
- 287 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Sulpiride: N‐[léthyl‐l pyrrolidinyl‐2) methyl] methoxy‐2 sulfamoyl‐5 benzamide, has been labelled with carbon 14 in the carbonyl group by a five step synthesis from barium carbonate ^14^C. The specific activity of the final product is 37.6 mCi/mM (110 μCi/mg), and the radiochemical purity 99.5%. UV‐ and mass spectrometry confirm the identity of the labelled compound with the reference material, as well as the position labelled with ^14^C.
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