N-methyl pyridinium-p-toluene Sulfonate (NMPyTs) catalyzed synthesis of pyrano[۲,۳-c]pyrazoles

Publish Year: 1395
نوع سند: مقاله ژورنالی
زبان: English
View: 280

This Paper With 10 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_ICC-5-3_005

تاریخ نمایه سازی: 2 مهر 1398

Abstract:

Abstarct:A simple one-pot synthesis of pyrano[ ۲,۳-c]pyrazoles was developed by a three-component reaction of various benzaldehydes, malononitrile and ۱-phenyl or hydro-۳-methyl-۱H-pyrazol-۵(۴H)-one in the presence of N-methyl pyridinium p-toluene sulfonate (NMPyTs) as a catalyst. All of the synthesized compounds were identified by IR, ۱H NMR, ۱۳C NMR and mass spectroscopy techniques. In the mentioned method, the use of thermal condition is avoided. The key advantages of this process are high yields, shorter reaction times, easy work-up, and purification of products by the non-chromatographic method. The synthesis of pyrano[۲,۳-c] pyrazoles using NMPyTs as an efficient catalyst is the novel methodology work.

Authors

Vinod Kamble

Institute of Science, Dept. of Chemistry Nagpur

Giribala Bondle

Dept. of Chemistry Dr. BAMU, Abad.

Sandeep Atkore

Dept. of Biochemistry, Dr. BAMU, Abad

مراجع و منابع این Paper:

لیست زیر مراجع و منابع استفاده شده در این Paper را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود Paper لینک شده اند :
  • J.L. Wang, D. Lui, Z.J. Zhang, S. Shan, X. Han, ...
  • M.N. Nasr, M.M. Gineinah, Arch. Pharm. Med. Chem., 2002, 35, ...
  • V.K. Ahluwalia, A. Dahiya, V. Garg, Indian J. Chem., 1997, ...
  • S.C. Kuo, L.J. Huang, H.J. Nakamura, J. Med. Chem., 1984, ...
  • M.E. Zaki, H.A Soliman, O.A. Hiekal, A.E.Z. Rashad, Naturforsch. C., ...
  • N. Foloppe, L.M. Fisher, R. Howes, A. Potter, A.G.S. Robertson, ...
  • H. Junek, H. Aigner, XXXV, Chem. Ber., 1973, 106, 914-921. ...
  • H.H. Otto, Arch. Pharm., 1974, 307, 444-447. ...
  • (a) Y.A. Sharanin, L.N. Shcherbina, L.G. Sharanina, V.V. Puzanova, VI: ...
  • (a) A.M. Shestopalov, Y.M. Emeliyanova, A.A. Shestopalov, L.A. Rodinovskaya, Z.I. ...
  • G. Vasuki, K. Kandhasamy, Tetrahedron Lett., 2008, 49, 5636-5638. ...
  • A. Siddekha, A. Nizam, M.A. Pasha, Spectrochim. Acta A., 2011, ...
  • S.A. El-Assaly, Der Pharma Chem., 2011, 3(5), 81-86. ...
  • S. Gogoi, C.G. Zhao, Tetrahedron Lett., 2009, 50, 2252-2255. ...
  • K. Kanagaraj, K. Pitchumani, Tetrahedron Lett., 2010, 51, 3312-3316. ...
  • J. Ebrahimi, A. Mohanndi, V. Pakjoo, E. Bahramzadeh, A. Habibi, ...
  • J.M. Khurana, A. Chaudhary, Green Chem. Lett. Rev., 2012, 5, ...
  • H. Mecadon, I. Kharbangar, B.M. Laloo, M.R. Rohman, I. Kharkongor, ...
  • H.V.  Chavan, S.B. Babar, R.U. Hoval, B.P. Bandgar, Bull. Korean ...
  • M.B.M. Reddy, V.P. Jayashankara, M.A.  Pasha, Synth. Commun., 2010, 40, ...
  • H.G. Kathrotiya, R.G. Patel, M.P. Patel, J. Serb. Chem. Soc., ...
  • M.S. Wu, D.L. Kong, X.Z.  Zhang, Acta Cryst. E., 2011, ...
  • M.B.M. Reddy, M.A. Pasha, Indian J. Chem., 2012, (51B), 537-541. ...
  • J.M. Khurana, B. Nand, S. Kumar, Synth. Commun., 2011, 41, ...
  • P.V. Shinde, J.B. Gujar, B.B. Shingate, M.S. Shingare, Bull. Korean ...
  • M. Babaie, H. Sheibani, Arabian J. Chem., 2011, 4, 159-162. ...
  • S.H.S. Azzam, M.A. Pasha, Tetrahedron Lett., 2012, 53, 6834-6837. ...
  • M. Wu, Q. Feng, D. Wan, J. Ma, Synth. Commun., ...
  • A.S. Nagarajan, B.S.R. Reddy, Synlett., 2009, 2002-2004. ...
  • M. Bihani, P.P. Bora, G. Bez, J. Chem., 2013, 1-8. ...
  • J.F. Zhou, S.J. Tu, J.F. Zhu, S.J. Tu, H.Q. Zhu, ...
  • S.B. Guo, S.X. Wang, J.T. Li, Synth, Commun., 2007, 37, ...
  • J.M. Khurana, A. Chaudhary, Green Chem. Lett. Rev., 2012, 5, ...
  • T.S. Jin, R.Q.  Zhao, T.S. Li, Arkivoc., 2006, (xi) 176-182. ...
  • نمایش کامل مراجع