66971-55-9Relevant articles and documents
Synthesis of 3- and 5-hydrazino-1-methyl-4-nitropyrazoles
Baryshnenkova,Perevalov,Polyakov
, p. 1113 - 1113 (1997)
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Synthesis, crystal structure, spectroscopic and computational studies of 2-{1-[2-(1,3-dimethyl-4-nitro-1H-pyrazol-5-yl)hydrazono]ethyl}pyridine
Abushamleh, Ahmad S.,Abu-Safieh, Kayed A.,Khanfar, Monther A.,Assaf, Khaleel I.,Salameh, Bader A.,Alwahsh, Nisreen J.
, p. 224 - 235 (2019/08/01)
2-{1-[2-(1,3-Dimethyl-4-nitro-1H-pyrazol-5-yl)hydrazono]ethyl}-pyridine has been prepared from 5-hydrazino-1,3-dimethyl-4-nitro-1H-pyrazole and 2-acetylpyridine in an ethanolic solution. It crystallizes as an (E/Z) isomeric pair in the triclinic space group P-1 with the lattice parameters: a = 10.357(1) ?, b = 11.613(1) ?, c = 13.069(1) ?, α = 67.74(1)°, β = 70.77(1)°, γ = 67.92(1)°, volume = 1315.6(3) ?3, Z = 2. The isomeric pair (E/Z) is contained in the unit cell, where the N-H group is H-bonded to the pyridine nitrogen and to the oxygen of the nitro group in the Z-isomer and to the oxygen of the nitro group only in the E-isomer. NMR showed that the E-isomer is the major. DFT calculations were performed to further investigate the electronic properties of the synthesized compound.
5-Substituted derivatives of dipyrazolo[1,5-a:4',3'-e]pyrazine-6-carboxylic acids and esters
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, (2008/06/13)
New 5-substituted derivatives of dipyrazolo[1,5-a:4',3'-e]pyrazine-6-carboxylic acid, esters and their salts have the formula STR1 R1 is hydrogen, lower alkyl or phenyl-lower alkylene; R2 and R3 each is hydrogen or lower alkyl; X is oxygen or sulfur; and R4 is hydrogen, lower alkyl, phenyl-lower alkylene or amino-lower alkylene. The new compounds are useful as anti-inflammatory agents and immunosuppressive agents.