Novel Ring Contraction of 6-Azauracil Derivatives
✍ Scribed by Hanna Wojtowicz-Rajchel; Joanna Szczepkowska-Sztolcman; Andrzej Katrusiak; Krzysztof Golankiewicz
- Book ID
- 104202821
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 124 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
21008C with and without an electrophilic agent. Reactions of appropriate 6-azauracils with t-butyllithium and lithium diisopropylamide gave, as a result of a ring contraction, compounds 5 and 6. The structure of compound 5 was undeniably established by X-ray analysis. A mechanism of the novel ring transformation of 1,2,4-triazines to imidazoles is discussed.
📜 SIMILAR VOLUMES
In spite of the fact that a great number of several 4-substituted derivatives of phenazone has already been prepared, the only derivative with 6-azauracile cycle up to now is 4-(2-thio-6-azauraciI-5-yl)-phenazone, prepared by Schmid?'.
## Abstract By diazotization of 3‐(2‐aminophenyl)‐1,2‐dihydroquinoxaline 1c, its 3‐(4‐aminophenyl)‐isomer**2c**, 3‐(2‐aminobenzyl)‐1,2‐dihydroquinoxaline‐2‐one **3c** and its 3‐(4‐aminobenzyl)‐isomer **4c** and by azo coupling of formed diazonium salts with ethyl cyanoacetylcarbamate, corresponding