Rp. Frutos et Gp. Roth, SYNTHESIS AND CHARACTERIZATION OF A NOVEL RANITIDINE DIMER, Bioorganic & medicinal chemistry letters, 7(23), 1997, pp. 3045-3048
A route towards the synthesis of a ranitidine bulk drug product impuri
ty is described. This protocol involves acetyl chloride initiated oxon
ium ion generation and subsequent trapping to form the corresponding r
anitidine dimer (1). This synthesis allowed for structure verification
of the impurity and provided reference supplies for further analytica
l and toxicology investigations. (C) 1997 Elsevier Science Ltd.