Abstract
2-Amino-7-methyl-5-oxo-4-phenyl-4,5-dihydropyrano[3,2-c]pyran-3-carbonitrile, C16H12N2O3 is synthesized via one-pot multi-component reaction at room temperature using commercially available urea as inexpensive and environmentally benign organo-catalyst. Its structure is determined by single-crystal X-ray diffraction technique The crystals are monoclinic, a = 10.7357(12), b = 8.7774(8), c = 15.0759(16) Å, β = 103.575(11)°, Z = 4, sp. gr. P21/n, R = 0.0551 for 1696 observed reflections. The crystal structure is stabilized by N–H···N, C–H···O, and C–H···π interactions.
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References
G. Brahmachari, Handbook of Pharmaceutical Natural Products (Wiley-VCH Verlag GmbH, Weinheim, 2010).
T. Raj, R. K. Bhatia, A. Kapur, et al., Eur. J. Med. Chem. 45, 790 (2010).
W. Kemnitzer, J. Drewe, S. Jiang, et al., J. Med. Chem. 50, 2858 (2007).
D. Kumar, V. B. Reddy, S. Sharad, et al., Eur. J. Med. Chem. 44, 3805 (2009).
G. Brahmachari and B. Banerjee, ACS Sustainable Chem. Eng. 2, 411 (2014).
G. M. Sheldrick, Acta Crystallogr. A 64, 112 (2008).
L. J. Farrugia, J. Appl. Crystallogr. 30, 565 (1997).
L. J. Farrugia, J. Appl. Crystallogr. 32, 837 (1999).
M. Nardelli, J. Appl. Crystallogr. 28, 659 (1995).
A. L. Spek, Acta Crystallogr. D 65, 148 (2009).
S. K. Mohamed, M. Akkurt, M. N. Tahir, et al., Acta Crystallogr. E 68, o1965 (2012).
J. N. Low, J. Cobo, M. Nogueras, et al., Acta Crystallogr. C 59, o38 (2003).
F. H. Allen, O. Kennard, D. G. Watson, et al., J. Chem. Soc. Perkin Trans., 2, S1–19 (1987).
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Sharma, S., Banerjee, B., Brahmachari, G. et al. Synthesis, characterization, and crystal structure of 2-amino-7-methyl-5-oxo-4-phenyl-4,5-dihydropyrano[3,2-c]pyran-3-carbonitrile. Crystallogr. Rep. 60, 1126–1130 (2015). https://doi.org/10.1134/S1063774515070238
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DOI: https://doi.org/10.1134/S1063774515070238