Abstract

In the title compound, C35H47ClN4O, the two pyrrolidine rings have envelope conformations. The conformation of the macrocycle is stabilized by N—H⋯N hydrogen bonds and a C—H⋯N inter­action. The benzoyl ring is inclined to the adjacent pyrrole ring by 11.66 (11)°, with a centroid–centroid distance of 3.7488 (13) Å. In the crystal, molecules are linked by N—H⋯O hydrogen bonds into helical chains propagating in [010] and C—H⋯O and C—H⋯π interactions are also observed.

Highlights

  • In the title compound, C35H47ClN4O, the two pyrrolidine rings have envelope conformations

  • The conformation of the macrocycle is stabilized by N—H N hydrogen bonds and a

  • The benzoyl ring is inclined to the adjacent pyrrole ring by 11.66 (11), with a centroid–centroid distance of 3.7488 (13) Å

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Summary

Data collection

H atoms treated by a mixture of independent and constrained refinement max = 0.24 e Å3. R factor = 0.053; wR factor = 0.102; data-to-parameter ratio = 15.5. C35H47ClN4O, the two pyrrolidine rings have envelope conformations. The conformation of the macrocycle is stabilized by N—H N hydrogen bonds and a. The benzoyl ring is inclined to the adjacent pyrrole ring by 11.66 (11) , with a centroid–centroid distance of 3.7488 (13) Å. Molecules are linked by N—H O hydrogen bonds into helical chains propagating in [010] and C—H O and C—H interactions are observed

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