S. Massa et al., RESEARCH ON NITROGEN-CONTAINING HETEROCYCLIC-COMPOUNDS .20. SYNTHESISOF H-IMIDAZO[5,1-C]PYRROLO-[1,2-A][1,4]BENZODIAZEPINE AND ITS 6-DERIVATIVES, Journal of heterocyclic chemistry, 30(3), 1993, pp. 749-753
Starting from 1H-1-(2-aminomethylphenyl)pyrrole the synthesis of H-imi
dazo[5,1-c]pyrrolo[1,2-a][1,4]benzodiazepine, a novel nitrogen contain
ing tetracyclic ring, has been performed by two routes involving a thr
ee-step and a six-step sequence, respectively. The more complex sequen
ce offers the advantage to obtain also 3-alkyl and 3-aryl derivatives
of the parent nucleus. The three step sequence involves the use of tol
uene-4-sulfonylmethylisocyanide (TosMIC) as a synthon.