Synthesis and Characterization of 7 - (3 - (substituted-phenoxy) propoxy) Quinazoline Derivatives

Article Preview

Abstract:

Four compounds of 7-(3- (substituted-phenoxy) propoxy) quinazoline compounds, including 7-(3-(2,4-dichlorophenoxy) propoxy)-N-(3-chlorophenyl)-6-methoxyquinazolin-4-amine, 7-(3-(2-chlo-rophenoxy) propoxy)-N-(3-chlorophenyl)-6-methoxyquinazolin-4-amine, 7-(3-(4-chlorophenoxy) prop-oxy)-N-(3-chlorophenyl)-6-methoxyquinazolin-4-amine, 7-(3-(naphthalen-3-yloxy) propoxy)-N-(3-chl-orophenyl)-6-methoxyquinazolin-4-amine, were synthesized from N-(5-(3-chloropropoxy)-2-cyano-4-methoxyphen-yl)-N, N-dimethylformamidine by cyclization,etheration, in the yield of 45.9%50.6%56.34% and 80.6% respectively. Their structures were characterized by IR, 1H NMR, 13C NMR, MS and elemental analysis.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 781-784)

Pages:

1003-1006

Citation:

Online since:

September 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] Y. Yarden, M. X. Sliwkowski. Nat. Rev. Mol. Cell. Biol. 2001, 2: 127-137.

Google Scholar

[2] S. Teman, H. Kawaguchi, A. K. El-Naggar, et al. J. Clin. Oncol. 2007, 25: 2164-2170.

Google Scholar

[3] F. Ciardiello, G. Tortora. Clin. Cancer Res. 2001, 7(10): 2958-2970.

Google Scholar

[4] (a) A. J. Bridges, H. Zhou, D. R. Cody, et al. J. Med. Chem. 1996, 39: 267-276. (b) M. Bos, J. Mendelsohn, Y. M. Kim, et al. Clin. Cancer Res. 1997, 3(11): 2099-2106.

Google Scholar

[5] A. A. Adjei, Drugs Future. 2001, 26(11): 1087-1092.

Google Scholar

[6] S. S. W. Ng, M. -S. Tsao, T. Nicklee, et al. Mol. Cancer Ther. 2002, 1: 777-783.

Google Scholar

[7] J. A. Bikker, N. Brooijmans, A. Wissner, et al. J. Med. Chem. 2009, 52(6): 1493-1502.

Google Scholar

[8] L. F. Hennequin,; E. S. E. Stokes, A. P. Thomas, et al. J. Med. Chem. 2002, 45: 1300-1312.

Google Scholar

[9] X. Cai, H. X. Zhai,; J. Wang, et al. J. Med. Chem. 2010, 53: 2000-(2009).

Google Scholar

[10] J. Domarkas, F. Dudouit, C. Williams, et al. J. Med. Chem. 2006, 49: 3544-3552.

Google Scholar

[11] A. Antonello, A. Tarozzi, F. Morroni, et al. J. Med. Chem. 2006, 49: 6642-6645.

Google Scholar

[12] H. -R. Tsou, N. Mamuya, B. D. Johnson, et al. J. Med. Chem. 2001, 44: 2719-2734.

Google Scholar

[13] X. D. Zhang, G. J. Xie, D. W. S. Chalisi, Z. Z. Chen, X. Chen. CN: 03108814. 7, (2004).

Google Scholar

[14] L. F. Hennequin, A. P. Thomas, C. Johnstone, et al. J. Med. Chem. 1999, 42: 5369-5389.

Google Scholar

[15] L. F. Hennequin, E. S. E. Stokes, A. P. Thomas, et al. J. Med. Chem. 2002, 45: 1300-1312.

Google Scholar

[16] C. Ditchfield, V. L. Johnson, A. Tighe, et al. The Journal of Cell Biology, 2003, 161: 267-280.

Google Scholar

[17] P. A. Ple´, T. P. Green, L. F. Hennequin, et al. J. Med. Chem. 2004, 47: 871- 887.

Google Scholar

[18] L. F. Hennequin, J. Allen, J. Breed, J. Curwen, et al. J. Med. Chem. 2006, 49: 6465- 6488.

Google Scholar

[19] K. M. Foote, A. A. Mortlock, N. M. Heron, et al. Bioorg. Med. Chem. Lett. 2008, 18: 1904-(1909).

Google Scholar

[20] H. P. Yan, G. P. Ouyang. Chinese Journal of Organic Chemistry, 2011, 31(6): 901-907. (In Chinese).

Google Scholar

[21] H. P. Yan, G. P. Ouyang. Fine Chemical Intermediates, 2010, 40(5): 40-42. (In Chinese).

Google Scholar