Halogen-Containing 2-methylpyrimido[1,2-a]-benzimidazol-4(10H)-ones / Ulomskiy E.N., El'Tsov O.S., Borisov S.S., Savateev K.V., Voinkov E.K., Fedotov V.V., Rusinov V.L. // Chemistry of Heterocyclic Compounds. - 2014. - V. 50, l. 7. - P. 1005-1013.

ISSN:
00093122
Type:
Article
Abstract:
We have synthesized a series of 3-halo-substituted pyrimidobenzimidazolones and studied the alkylation reaction of the obtained derivatives. © 2014 Springer Science+Business Media New York.
Author keywords:
alkylation; azolopyrimidines; halogenation; nitrogen heterocycles; pyrimido[1,2-a]benzimidazol-4(10H)-one
Index keywords:
нет данных
DOI:
10.1007/s10593-014-1556-6
Смотреть в Scopus:
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84919914564&doi=10.1007%2fs10593-014-1556-6&partnerID=40&md5=513b9e9c2d2e642c427c9f24c428f2df
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Link https://www.scopus.com/inward/record.uri?eid=2-s2.0-84919914564&doi=10.1007%2fs10593-014-1556-6&partnerID=40&md5=513b9e9c2d2e642c427c9f24c428f2df
Affiliations Ural Federal University Named after the First President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, Russian Federation
Author Keywords alkylation; azolopyrimidines; halogenation; nitrogen heterocycles; pyrimido[1,2-a]benzimidazol-4(10H)-one
References Swan, S.K., Smith, W.B., Marbury, T.C., Schumacher, M., Dougherty, C., Mico, B.A., Villano, S.A., (2007) J. Clin. Pharmacol., 47, p. 209. , 1:CAS:528:DC%2BD2sXitVClsbo%3D; Chou, S., Marousek, G.I., (2006) Antimicrob. Agents Chemother., 50, p. 3470. , 1:CAS:528:DC%2BD28XhtVylsbbP; Jones, E.D., Vandegraff, N., Le, G., Choi, N., Issa, W., Macfarlane, K., Thienthong, N., Deadman, J.J., (2010) Bioorg. Med. Chem. Lett., 20, p. 5913. , 1:CAS:528:DC%2BC3cXhtFGnt73K; Chiba, T., Shigeta, S., Numazaki, Y., (1995) Biol. Pharm. Bull., 18, p. 1081. , 1:CAS:528:DyaK2MXotlGnsLo%3D; Wilcken, R., Zimmermann, M.O., Lange, A., Joerger, A.C., Boeckler, F.M., (2013) J. Med. Chem., 56, p. 1363. , 1:CAS:528:DC%2BC38Xhs1GrurfJ; Di Braccio, M., Grossi, G., Signorello, M.G., Leoncini, G., Cichero, E., Fossa, P., Alfei, S., Damonte, G., (2013) Eur. J. Med. Chem., 62, p. 564; Da Settimo, A., Primofiore, G., Da Settimo, F., Marini, A.M., Taliani, S., Salerno, S., Dalla Via, L., (2003) J. Heterocycl. Chem., 40, p. 1091; Witvrouw, M., Daelemans, D., Pannecouque, C., Neyts, J., Andrei, G., Snoeck, R., Vandamme, A.M., De Clercq, E., (1998) Antivir. Chem. Chemother., 9, p. 403. , 1:CAS:528:DyaK1cXmsFCntbk%3D; Filipponi, E., Cruciani, G., Tabarrini, O., Cecchetti, V., Fravolini, A., (2001) J. Comput. Aided Mol. Des., 15, p. 203. , 1:CAS:528:DC%2BD3MXitlWjt7c%3D; Hermecz, I., (1984) Synthesis, p. 152; Ogura, H., Kawano, M., Itoh, T., (1973) Chem. Pharm. Bull., 21, p. 2019. , 1:CAS:528:DyaE3sXltlOjtbY%3D; Ulomskiy, E.N., Medvedeva, N.R., Shchepochkin, A.V., Eltsov, O.S., Rusinov, V.L., Chupakhin, O.N., Deyeva, E.G., Kiselev, O.I., (2011) Chem. Heterocycl. Compd., 47, p. 1164. , 1:CAS:528:DC%2BC3MXhs1Grt73O; Bohme, H., Weisel, K.H., (1976) Arch. Pharm. (Weinheim), 309, p. 959. , 1:STN:280:DyaE2s7jtlGktg%3D%3D; Sirko, S.M., Gorobets, N.Y., Musatov, V.I., Desenko, S.M., (2009) Molecules, 14, p. 5223. , 1:CAS:528:DC%2BD1MXhsF2gurbL; Puttaraju, K.B., Shivashankar, K., Chandra, Mahendra, M., Rasal, V.P., Venkata Vivek, P.N., Rai, K., Beebina Chanu, M., (2013) Eur. J. Med. Chem., 69, p. 316. , 1:CAS:528:DC%2BC3sXhslart7rN; http://shelx.uni-ac.gwdg.de/SHELX/download.php
Correspondence Address Ulomskiy, E.N.; Ural Federal University Named after the First President of Russia B. N. Yeltsin, 19 Mira St., Russian Federation
Publisher Springer New York LLC
CODEN CHCCA
Language of Original Document English
Abbreviated Source Title Chem. Heterocycl. Compd.
Source Scopus