Synthesis of tritium labeled 1-amidino-3-(P-nitro-phenyl)urea: A potential antimalarial agent
✍ Scribed by Theodore S. T. Wang; Rashid A. Fawwaz; Ronald L. van Heertum
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 219 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Five steps were required to synthesize the title compound. This involved a catalytic exchange reaction, nitration, hydrolysis, and condensation. The overall radiochemical yield was 28.87% and the specific activity was 12.4 mCi/mmol, with a radiochemical purity of more than 95.7%.
📜 SIMILAR VOLUMES
## Abstract The title compound was prepared by the LiAlT~4~ reduction of 5‐fluoro‐3‐[3‐[4‐(5‐methoxy‐4‐pyrimidinyl)‐1‐piperazinyl]‐3‐oxopropyl]‐1H‐indole. The radiochemical purity of the product was 98.9% and the specific activity was calculated as 53.0 Ci/mmol from HPLC analyses and 55.6 Ci/mmol f