Two o f t h e m i n o r m e t a b o l i t e s o f t h e a n t i t h y r o i d d r u g 6 -p r o p y l -2t h i o u r a c i l ( I ) have been i s o l a t e d f r o m r a t u r i n e i d e n t i f i e d as S-methyl-6 -p r o p y l -2 -t h i o u r a c i l
Synthesis of 6-n-propyl-2-thiouracil-6−14C
✍ Scribed by D. P. Thornhill; D. S. Sitar
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- French
- Weight
- 202 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
6‐n‐Propyl‐2‐thiouracil‐6−^14^C was prepared from sodium butyrate‐1−^14^C, with a radiochemical yield of 34%. Butyryl chloride‐1−^14^C was prepared from butyric acid‐1−^14^C and condensed with sodio ethylacetoacetate to yield ethyl β‐oxohexanoate‐β−^14^C. The β‐keto ester was condensed with thiourea in sodium ethoxide to yield the 2 substituted thiouracil.
📜 SIMILAR VOLUMES
## Abstract Synthesis of 6‐/N,N‐1′, 6′‐hexyleneformamidine‐^14^C/penicillanic acid /VII/ was carried out. N‐formyl‐^14^C‐hexamethyleneimine /II/ was obtained from formic‐14C acid and hexamethyleneimine /I/. The product was chlorinated with oxalyl chloride. The obtained N,N‐1, 6‐hexylenechloroformim
## Abstract For Abstract see ChemInform Abstract in Full Text.