2369-89-3Relevant academic research and scientific papers
7-Amino-2,5-dimethylpyrazolo[1,5-a]-pyrimidine hemihydrate redetermined at 120 K: A three-dimensional hydrogen-bonded framework
Portilla, Jaime,Quiroga, Jairo,Cobo, Justo,Low, John N.,Glidewell, Christopher
, p. o186-o189 (2006)
In the title compound, C8H10N4·0. 5H2O, where the water molecules lie on twofold rotation axes in the space group C2, the components are linked by three hydrogen bonds, one each of O-H...N, N-H...N and N-H...O types, into a complex three-dimensional framework structure.
Synthesis of novel 5-amino-1-aroylpyrazoles
Quiroga, Jairo,Portilla, Jaime,Abonía, Rodrigo,Insuasty, Braulio,Nogueras, Manuel,Cobo, Justo
body text, p. 5943 - 5945 (2009/04/11)
A series of 5-amino-1-aroylpyrazoles 3 are synthesized directly by the reaction of β-aminocrotononitrile 1 with some structures containing the hydrazine moiety (X-NHNH2) 2 by refluxing ethanol in presence of sodium acetate. When semicarbazide 3i was used (X = CONH2), the reaction afforded the unexpected 7-aminopyrazolo[1,5-a]pyrimidine 4.
Pyrazolo[1,5-a]pyrido[3,2-e]pyrimidine-7-carboxylic acid derivatives
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, (2008/06/13)
New derivatives of pyrazolo[1,5-a]pyrido[3,2-e]-pyrimidine-7-carboxylic acid have the general formula STR1 The new compounds are useful as central nervous system depressants and an anti-inflammatory agents.
