Studies on Phenazines. XV. The Ring Cleavage of Phenazine. (1). 2, 3-Quinoxalinedicarboxylic Acid
Oxidation of phenazine gave 2, 3-quinoxalinedicarboxylic acid in the yield of 70%, together with small amount of another acidic substance. The latter was obtained by the similar oxidation of 1-and 2-methoxyphenazine in the yields of 45% and 24%, respectively. From quinoxalinedicarboxylic acid, 2-qui...
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Published in | Pharmaceutical Bulletin Vol. 5; no. 3; pp. 277 - 279 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Japan
The Pharmaceutical Society of Japan
1957
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Abstract | Oxidation of phenazine gave 2, 3-quinoxalinedicarboxylic acid in the yield of 70%, together with small amount of another acidic substance. The latter was obtained by the similar oxidation of 1-and 2-methoxyphenazine in the yields of 45% and 24%, respectively. From quinoxalinedicarboxylic acid, 2-quinoxaline-carbonamide, -carbohydrazide, and -hydroxamic acid were prepared and their antitubercular activities tested. |
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AbstractList | Oxidation of phenazine gave 2, 3-quinoxalinedicarboxylic acid in the yield of 70%, together with small amount of another acidic substance. The latter was obtained by the similar oxidation of 1-and 2-methoxyphenazine in the yields of 45% and 24%, respectively. From quinoxalinedicarboxylic acid, 2-quinoxaline-carbonamide, -carbohydrazide, and -hydroxamic acid were prepared and their antitubercular activities tested. |
Author | Yosioka, Itiro Otomasu, Hirotaka |
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Title | Studies on Phenazines. XV. The Ring Cleavage of Phenazine. (1). 2, 3-Quinoxalinedicarboxylic Acid |
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