The title compound, C 12 H 14 N 6 , was synthesized via cyclocondensation of 5-amino-1-guanyl-3-phenyl-1,2,4-triazole with acetone. Only one tautomeric form with an H atom at the triazine N atom was observed in the crystal structure. The compound crystallizes with two almost identical molecules in t
Synthetic approaches to 5,7-disubstituted imidazo[5,1-f][1,2,4]triazin-4-amines
โ Scribed by Douglas S. Werner; Hanqing Dong; Mridula Kadalbajoo; Radoslaw S. Laufer; Paula A. Tavares-Greco; Brian R. Volk; Mark J. Mulvihill; Andrew P. Crew
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 391 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The preparation of 5,7-disubstituted imidazo [5,1-f ][1,2,4]triazin-4-amines, exemplified by 5-[3-(benzyloxy)phenyl]-7-cyclobutylimidazo[5,1-f ][1,2,4]triazin-4-amine, was developed through a linear and three convergent synthetic strategies, with the latter providing the greatest flexibility for diversification at the 5-position at the last step of the synthesis.
๐ SIMILAR VOLUMES
The title compound, C 12 H 14 N 6 , was synthesized via cyclocondensation of 5-guanidino-3-phenyl-1,2,4-triazole with acetone. Only one tautomeric form with the NH H atom vicinal to the methyl groups was observed in the crystal structure. The triazine ring adopts a flattened half-boat conformation.