Synthesis of 2-Alkylamino/Alkoxy-3-Arylthieno[3,2-d]Pyrimidin-4(3H)-One Derivatives

Qiu Hong Dai; Quan Bin Liao; Nian Yu Huang; Ming Guo Liu

doi:10.4028/www.scientific.net/AMR.740.469

Paper Titles

Enhancement of Dispersion Stability of Carbon Nanotube in Solvents
p.449

Blocked Polyurethane/Tetrabromo Vinyl Ester Interpenetrating Polymer Networks: Thermal and Flame Retardant Properties
p.455

The Research of Structural Parameters on Natural Frequency of Laminated Composite Plates
p.461

Synthesis of the Novel Compounds 2-Lactosylthio-3-Alkyl/Alkoxythieno[3,2-d]Pyrimidin-4(3H)-Ones
p.465

Synthesis of 2-Alkylamino/Alkoxy-3-Arylthieno[3,2-d]Pyrimidin-4(3H)-One Derivatives
p.469

Corrosion Protection of Mg Alloy by a TiO₂ Coating Prepared by Sol-Gel Method
p.473

Influence of Metal Ions on β-D-glucosidase Activity, Growth and Astaxanthin Production of Xanthophyllomyces dendrorhous
p.478

Nanoscale Order in ZnTe:(Cd, O)
p.483

The Influence of Nanofilled Aluminum Oxide on Electrical Tree Growth Behavior under High Voltage Non-Uniform Field Stress
p.488

HomeAdvanced Materials ResearchAdvanced Materials Research Vol. 740Synthesis of...

Synthesis of 2-Alkylamino/Alkoxy-3-Arylthieno[3,2-d]Pyrimidin-4(3H)-One Derivatives

Abstract:

The title compounds 2-alkylamino/alkoxy-3-arylthieno [3,2-pyrimidin-4(3H)-ones were synthesized by base catalytic reactions of primary amines or alcohols with carbodiimides,which were obtained from the aza-wittig reaction of iminophosphorane 2 and arylisocyanates.The conditions of cyclization and spectral properties were researched.

You might also be interested in these eBooks

Materials, Mechatronics and Automation II

View Preview

Info:

Periodical:

Advanced Materials Research (Volume 740)

Pages:

469-472

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.740.469

Citation:

Cite this paper

Online since:

August 2013

Authors:

Qiu Hong Dai, Quan Bin Liao, Nian Yu Huang, Ming Guo Liu

Keywords:

Aminothiophene, Aza-Wittig Reaction, Carbodiimide, Iminophosphorane, Thieno[3,2-d]pyrimidin-4(3H)-One

Export:

RIS, BibTeX

Price:

Permissions CCC:

Request Permissions

Permissions PLS:

Request Permissions

Сopyright:

Citation:

References

[1] M.W. Ding, S.Z. Xu, J.F. Zhao: The Journal of Organic Chemistry. 69 (2004), p.8366.

Google Scholar

[2] R.V. Chambhare, B.G. Khadse, A.S. Bobde, R.H. Bahekar: European Journal of Medicinal Chemistry. 38 (2003), p.89.

Google Scholar

[3] Y.D. Wang, S. Johnson, D. Powell, J.P. McGinnis, M. Miranda S.K. Rabindran. Bioorganic & Medicinal Chemistry Letters. 15 (2005), p.3763.

DOI: 10.1016/j.bmcl.2005.05.127

Google Scholar

[4] L.D. Jennings, S.L. Kincaid, Y.D. Wang, G. Krishnamurthy, C.F. Beyer, J.P. McGinnis, M. Miranda, C.M. Discafani S.K. Rabindran: Bioorganic & Medicinal Chemistry Letters. 15 (2005), p.4731.

DOI: 10.1016/j.bmcl.2005.07.072

Google Scholar

[5] F. Al-Omran, A.A. El-Khair: Journal of Heterocyclic Chemistry. 41(2004), p.909.

Google Scholar

[6] M.W. Ding, Y.F. Chen, N.Y. Huang: European Journal of Organic Chemistry. 18 (2004), p.3872.

Google Scholar

[7] Q.B. Liao, M.G. Liu, L. Yu, M. Zhu, M.W. Ding: Chinese Journalof Organic Chemistry. 29 (2009), p.1582.

Google Scholar

[8] M.G. Liu, Y. Zhong, M.W. Ding: Chemical Research in Chinese Universities. 24 (2008), p.437.

Google Scholar

[9] D. Vazquez, C. Peinador, J.M. Quintela: Tetrahedron. 60 (2004), p.275.

Google Scholar

[10] Y.G. Hu, A.H. Zheng, X.Z. Ruan, M.W. Ding: Beilstei Journal organic Chemistry. 24 (2008), p.49.

Google Scholar