Synthesis of 14C-labelled 2,4,-diamino-5-phenylthiazole hydrochloride (amiphenazole)
✍ Scribed by Jeffrey G. Adams; Paul J. Nicholls; Hywel Williams
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 155 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis of 2,4‐diamino‐5‐phenylthiazole hydrochloride labelled with carbon – 14 in the 2‐position has been effected whereby the ^14^C‐label was introduced in the last step. The overall yields were 34.5% (gravimetrically) and 32.8% (radiochemically).
📜 SIMILAR VOLUMES
## Abstract Radioisotopic labelling of a novel histamine level reducing and antiinflammatory agent is described. The 2‐hydroxy‐5‐carbomethoxybenzy ‐^14^C‐oxyamine hydrochloride was prepared for the purpose of radioisotopic indication and further for pharmacological and action mechanism studies.
## Abstract ^14^C‐labelled (S)‐(+)‐2‐[4‐(p‐fluorobenzoyl)‐1‐piperidyl]‐1‐naphthylethanol hydrochloride (5), an anti‐ischemic drug, was synthesized for studying the pharmacokinetic profiles of the compound in four steps using 2‐[carbonyl‐^14^C]acetonaphthone (1) as a labelled starting material.
## Abstract A method of carbon‐^14^C introduction into the molecule of a new drug 4‐methyl‐2‐pyridyl‐2‐furamide hydrochloride /MEPAF/ has been elaborated and furan‐2‐^14^C‐carboxylic acid has been synthesized. Radioactivity distribution and chemical yields in this synthesis were established.