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Synthesis, molecular and crystal structure of new 9,10-substituted deazaflavins

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Abstract

Cyclocondensation of 6-N-(3-hydroxypropyl)aminouracyl with 2-fluoro- or 2,3-dimethoxy-substituted benzaldehydes provided the corresponding 9,10-substituted 5-deazaflavins {pyrimido[4,5-b]quinoline-2,4-(3H,10H)diones}. X-ray diffraction analysis was carried out for 9-methoxy-10-(3-hydroxy-propyl)-substituted 5-deazaflavin derivative.

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Correspondence to R. G. Melik-Ohandzanyan.

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Original Russian Text © R.G. Melik-Ohandzanyan, T.R. Hovsepyan, S.G. Israelyan, R.A. Tamazyan, A.G. Ayvazyan, G.A. Panosyan, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 8, pp. 1178–1180.

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Melik-Ohandzanyan, R.G., Hovsepyan, T.R., Israelyan, S.G. et al. Synthesis, molecular and crystal structure of new 9,10-substituted deazaflavins. Russ J Org Chem 50, 1161–1163 (2014). https://doi.org/10.1134/S1070428014080156

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  • DOI: https://doi.org/10.1134/S1070428014080156

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