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. 2011 Dec 1;67(Pt 12):o3386-7.
doi: 10.1107/S1600536811048306. Epub 2011 Nov 19.

(2R)-4-[(9H-Fluoren-9-ylmeth-oxy)carbon-yl]-2-methyl-piperazin-1-ium chloride

(2R)-4-[(9H-Fluoren-9-ylmeth-oxy)carbon-yl]-2-methyl-piperazin-1-ium chloride

Anne Ertan et al. Acta Crystallogr Sect E Struct Rep Online. .

Abstract

The synthesis of the title salt, C(20)H(23)N(2)O(2) (+)·Cl(-), was carried out with a precursor of known absolute configuration (R) and the X-ray analysis confirmed that the product retained the absolute configuration. In the crystal, the dominant packing motif is a chain running along [010] generated by N-H⋯Cl hydrogen bonding. C-H⋯O and C-H⋯Cl inter-actions are also observed.

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Figures

Fig. 1.
Fig. 1.
Scheme I and II showing the two possible mono protected products, not possible to elucidate their structures by chromatographic or spectroscopic analysis.
Fig. 2.
Fig. 2.
View of the title compound showing the atom-labelling scheme. Displacement ellipsoids of non-H atoms are drawn at the 50% probability level. ORTEPII (Johnson, 1976).
Fig. 3.
Fig. 3.
Part of the molecular H-bond scheme with the molecules joined as chains containg equivalent symmetry translated units along the [1 0 0] direction. Dotted lines indicate H-bond interactions. The view is along the [1 0 0] direction. PLATON (Spek, 2009).
Fig. 4.
Fig. 4.
Spacefill packing diagram of the molecules in the unit cell along the [1 0 0] direction reflecting an efficient molecular packing arrangement. PLATON (Spek, 2009).

References

    1. ACD (2011). ACD/Labs Advanced Chemistry Development Inc., Toronto, Ontario, Canada.
    1. Altomare, A., Burla, M. C., Camalli, M., Cascarano, G. L., Giacovazzo, C., Guagliardi, A., Moliterni, A. G. G., Polidori, G. & Spagna, R. (1999). J. Appl. Cryst. 32, 115–119.
    1. Cho, Y. S., Borland, M., Brain, C., Chen, C. H.-T., Cheng, H., Chopra, R., Chung, K., Groarke, J., He, G., Hou, Y., Kim, S., Kovats, S., Lu, Y., OReilly, M., Shen, J., Smith, T., Trakshel, G., Vogtle, M., Xu, M., Xu, M. & Sung, M. J. (2010). J. Med. Chem. 53, 7938–57. - PubMed
    1. Flack, H. D. (1983). Acta Cryst. A39, 876–881.
    1. Johnson, C. K. (1976). ORTEPII Oak Ridge National Laboratory, Tennessee, USA