## Abstract The synthesis from carbonβ^14^C dioxide of 1, 3βdihydroβ1βmethylβ7βnitroβ5βphenylβ2Hβ1, 4βbenzodiazepinβ2βoneβ5β^14^C (I) for use in metabolic studies has been described. The synthesis was achieved by the sequence shown in figure 1. The overall yield of labelled nimetazepam (I) was near
Synthesis and characterization of 2-hydroxymethyl-1-methyl-4-nitro-5-imidazolcarbonitrile-4, 5-14C
β Scribed by Robert L. Ellsworth; Henry T. Meriwether; Holly E. Mertel
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 306 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
Preparation of the title compound, a key intermediate required to assist in the investigation and development of a new class of substances for controlling coccidiosis, is described. This labeled substance was synthesized in 10 steps, with a 17% overall radiochemical yield, from oxalicβ1,2β^14^C acid.
π SIMILAR VOLUMES
A synthesis of 3-cyano-4-methyl-5 ( 14 C)-methyl-2-(5-14C)pyrrolyloxamic acid is described. The compound, having specific activity of 66.7 pCi/mmole, was obtained in 19.68% overall yield from uniformly labelled 14C-l-alanine. 14 14 Key Words: 3-Cyano-4-methyl-5( C)-methyl-2-(5-C)pyrrolyloxamic acid,
A simple four-stage conversion of 2-1nethyl-4(5>nitroimidazole to 2-methyl-4(5)-nitr0['~N""]imidazole is reported. The method consists in N-nitration of the initial compound to ?-methyl-1,4-dinitroimidazole, treating the latter with ["Nlglycine and N-dealkylation of the obtained (~-rnethyl-4-nitro[~
## Synthesis of l-Methyl-4-(5-14C-3-methyl-5-isoxazolyl) pyridinium Chloride Received on 21st November 1968 l-Methyl-4-(3-methyl-5-isoxazolyl)pyridinium chloride (1) has been found to display interesting hypoglycemic activity in laboratory animals, and is currently undergoing extensive evaluation