## Abstract The preparation of ^14^C labelled 1‐(4‐chlorophenyl)‐2‐methy 1‐2‐aminopropane hydrochloride is described. The radioactive carbon was introduced into the central position of the aminopropyl group in order to study the pharmacological properties and mode of action of the anorexigenic drug
Synthesis of 14C-labelled 1-(2,6-dimethyphenylamino)-2-dimethylamino-propane
✍ Scribed by G. Zólyomi; Z. Zubovics; L. Toldy
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 245 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
The antiarrhytmic 1-(2,6-dimethylphenylamin0)-2--dimethylamino-propane (&) was labelled with I4C for pharmacokinetic study. A convenient synthesis, using 2-brom0propionyl-l-~~C chloride as radioactive key intermediate, involving an improved method for the reduction of N-( 2-dimethylaminopropionyl)-2,6--dimethylaniline (8) was elaborated.
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## Abstract ^14^C‐Labelled myosmine ([2′‐^14^C]‐3‐(1‐pyrrolin‐2‐yl)pyridine) was synthesized for autoradiography studies starting from [carboxyl‐^14^C]‐nicotinic acid by initial esterification of the latter in the presence of 1,1,1‐triethoxyethane. Without any purification the ethyl nicotinate form
## Abstract 4‐|2‐(Dimethylamino)ethyl‐2‐^14^C| phenol (hordenine‐α‐^14^C) has been synthesised in three steps from |^14^C|potassium cyanide and __p__‐benzyloxybenzyl chloride which in turn was obtained in four steps from __p__‐hydroxybenzoic acid.
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