## Abstract In the first publication in this series it was shown that only partial reduction of the pyrazine ring occurs in the catalytic hydrogenation of tetra‐carbethoxypyrazine. The remaining double bonds in the resultant reaction product are apparently stabilised. In agreement with the hypothes
Investigations on pyrazine derivatives. VII: On the conversion of pyrazine 2,5-dicarboxylic acid into some derivatives of 2-aminopyrazine 5-carboxylic acid
✍ Scribed by W. J. Schut; H. I. X. Mager; W. Berends
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 445 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Pyrazine 2,5‐dicarboxylic acid was prepared by oxidation of 2,5‐dimethylpyrazine with selenium dioxide. 2,5‐Diethoxycarbonylpyrazine appeared to be a suitable starting‐material for the preparation of monocarbamoyl‐ and monocarboxyhydrazide derivatives. Hofmann degradation of 2‐carbamoyl‐5‐ethoxycarbonylpyrazine into 2‐aminopyrazine 5‐carboxylic acid proved to be rather difficult. The monocarboxyhydrazides in this series could be readily converted into acid azides and eventually into pyrazine‐urethanes.
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