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Synthesis and crystal structure of ()-2-(6-chloroimidazo[1,2-]pyridin-2-yl)-3-[4-(di-methyl-amino)phen-yl]acrylo-nitrile.

クロロイミダゾピリジン誘導体アクリロニトリル化合物の合成と結晶構造解析

other not specified not assessed

Abstract

The crystal structure of a compound incorporating a 6-chloroimidazo[1,2-a]pyridine unit linked to a dimethylaminophenyl-substituted acrylonitrile moiety was determined at 100 K. Within the crystal lattice, intermolecular C-H···N and C-H···Cl hydrogen bonds generate a network propagating along the [010] direction. C-H···π and π-π stacking interactions, together with additional intermolecular contacts, further stabilize the packing. Hirshfeld surface analysis quantified the relative contributions of key contacts: H···H at 30.2%, H···C/C···H at 28.6%, H···N/N···H at 19.9%, H···Cl/Cl···H at 12.2%, and C···C at 3.7%.

Bibliographic

Authors
Akonan L, Ziki E, N'guessan DUJ, Coulibaly S, Ouattara M, Adohi-Krou V
Journal
Acta Crystallogr E Crystallogr Commun
Year
2025 (2025-09-01)
PMID
40918573
DOI
10.1107/S2056989025007248
PMC
PMC12412701

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Delivery context

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

Safety notes

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

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Cite as: H2 Papers — PMID 40918573. https://h2-papers.org/en/papers/40918573
Source: PubMed PMID 40918573