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Co-crystallisation of 4-amino pyridine with succinic acid (1:1): spectroscopic, thermal, crystal structure, DFT/HF calculation and Hirshfeld surface analysis
Published in Molecular Physics, 2022
P. J. Srijana, Mulveer Singh, B. Narayana, B. K. Sarojini, U. Likhitha, Rajni Kant
Aminopyridines are N-heterocyclic amines with anti-bacterial and antithrombotic properties that have been used to treat various types of diseases [9]. In particular, 4-aminopyridine is the first drug molecule that is particularly used in the treatment of multiple sclerosis syndromes by blocking the potassium channel [10]. It has two hydrogen bond donors and two hydrogen bond acceptors, while in cationic form; it has three hydrogen bond donors. In general, 4-aminopyridine forms complexes with carboxylic acid, resulting in supra-molecular heterosynthon by establishing either neutral N–H···O or N+–H···O− hydrogen bonds. There are various reports in the literature on co-crystals and salts of 4-aminopyridine [11–16].