Abstract

The racemic title dipyrrolopyrrolizine compound crystallizes from dimethylformamide as a disolvate, C(55)H(39)Cl(2)N(7)O(6)·2C(3)H(7)NO. None of the four fused heterocyclic rings is planar; one adopts an envelope conformation, two others adopt half-chair conformations and the fourth adopts a conformation intermediate between an envelope and a half-chair. The arrangement of the ring fusions is such as to preclude the possibility of internal mirror symmetry. The three independent molecular components are weakly linked by C-H···O hydrogen bonds, and the dipyrrolopyrrolizine molecules are linked by a combination of four C-H···O and one C-H···π(arene) hydrogen bond to form a three-dimensional framework, from which the dimethylformamide solvent molecules are pendent. However, aromatic π-π stacking interactions are absent in the structure.

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