Specifically labelled phenylacetic acid and mandelic acid derivatives, metabolites of L-Dopa, have been synthesized via the intermediary labelled benzyl alcohols, which were prepared by reduction of the methyl esters of the appropriate benzoic acids. The benzyl alcohols have been converted to the co
Synthesis of 1-[2-hydroxy-4-(3-sulfo-1-propyloxy)-phenyl]- -3-(3-hydroxy-4-methoxyphenyl)-propan-1-one-1-14C sodium salt
✍ Scribed by E. Koltai; K. Esses-Reiter; D. Bánfi
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- French
- Weight
- 258 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
1‐[2‐hydroxy‐4‐(3‐sulfo‐1‐propyloxy)‐phenyl]‐3‐ ‐(3‐hydroxy‐4‐methoxyphenyl)‐propan‐1‐one sodium salt labelled with ^14^C at its carbonyl group (1) was synthetized starting from sodium acetate‐1‐^14^C through acetyl chloride‐1‐^14^C, resacetophenone‐carbonyl‐^14^C (2), 2‐hydroxy‐4‐(3‐sulfo‐1‐propyloxy)‐acetophenone‐carbonyl‐^14^C sodium salt (3) and 1‐[2‐hydroxy‐4‐(3‐sulfo‐1‐propyloxy)‐phenyl]‐3(3‐hydroxy‐4‐methoxyphenyl)‐2‐ propen‐1‐one‐1‐^14^C (4).
📜 SIMILAR VOLUMES
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Tema~epam-2-'~C, 7-Chloro-1,3-ihydro-3-hydroxy-1 -methyl-5-phenyl-2H-1,4-benzodiazepin-2-one--"C, was prepared in a f ive-step synthesis. Chl~roacetic-l-~~C acid was converted to the acid chloride with thionyl chloride. The acid chloride was allowed to react with 2-methylamino-5-chloro-benzophenone