Monastrol Synthesis Using Subcritical EtOH: Response Surface Method for Optimization

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 72

فایل این مقاله در 10 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_IJCCE-44-4_009

تاریخ نمایه سازی: 16 خرداد 1404

چکیده مقاله:

Monastrol is an Eg۵ inhibitor that induces mitotic arrest and apoptosis. The efficiency of the Biginelli reaction for Monastrol synthesis can be enhanced by utilizing a subcritical EtOH. The response surface method was employed to optimize the synthesis yield of subcritical EtOH by varying the parameters of temperature, pressure, and reaction time. The synthesis yield of Monastrol using the optimum subcritical EtOH method was compared with the flux method, both utilizing three different catalysts: sodium hydrogen sulfate, hydrochloric acid, and ytterbium trifluoromethanesulfonate. The synthesis yield of Monastrol using the optimum subcritical EtOH method was found to be significantly higher compared to the flux method. Furthermore, the catalysts sodium hydrogen sulfate and ytterbium trifluoromethanesulfonate exhibited improved synthesis yield in comparison to the acid-catalyzed reactions. Additionally, the findings obtained from thin-layer chromatography confirmed the results obtained from LC-MS analysis. This innovative approach can be extended to other heteroaromatic aldehydes

نویسندگان

Yousuf Karimi

Student Research Committee, Mashhad University of Medical Sciences, Mashhad, I.R. IRAN

Mojgan Nejabat

Department of Medicinal Chemistry, Mashhad University of Medical Sciences, Mashhad, I.R. IRAN

Hossein Kamali

Department of Pharmaceutics, Mashhad University of Medical Sciences, Mashhad, I.R. IRAN

Farzin Hadizadeh

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, I.R. IRAN

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله 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 مقاله لینک شده اند :
  • Sheykhi-Estalkhjani A., Mahmoodi N.O., Yahyazadeh A., Nadamani M.P., Nahzomi H.T., ...
  • Mahmoodi N.O., Ramzanpour S., Ghanbari Pirbasti F., One‐Pot Multi‐Component Synthesis ...
  • Biginelli P., The Urea-Aldehyde Derivatives of Acetoacetic Esters, Gazz. Chim. ...
  • Rogerio K., Vitório F., Kümmerle A., Graebin C., Reações Multicomponentes: ...
  • Sweet F., Fissekis J.D., Synthesis of ۳, ۴-Dihydro-۲ (۱h)-Pyrimidinones and ...
  • Kappe C.O.A., Reexamination of the Mechanism of the Biginelli Dihydropyrimidine ...
  • Kapoor T.M., Mayer T.U., Coughlin M.L., Mitchison T.J., Probing Spindle ...
  • Cochran J.C., Gatial J.E., Kapoor T.M., Gilbert S.P., Monastrol Inhibition ...
  • Debonis S., Et Al. Interaction of the Mitotic Inhibitor Monastrol ...
  • Duan L., Et Al. Centrin: Another Target of Monastrol, an ...
  • Abassi Y.A., Et Al. Kinetic Cell-Based Morphological Screening: Prediction of ...
  • Zhu L., Et Al. Synthesis and Biological Evaluation of Novel ...
  • Prashantha Kumar B., Et Al. Synthesis of Novel Hantzsch Dihydropyridines ...
  • Al-Zaydi K.M., Al-Boqami M., Elnagdi N.M., Green Synthesis of Dihydropyrimidines ...
  • Simurova N., Maiboroda O., Biginelli Reaction–An Effective Method for the ...
  • Gilani A.G., Yazdanbakhsh M., Mahmoodi N., Moghadam M., Moradi E., ...
  • Kappe C.O., Recent Advances in the Biginelli Dihydropyrimidine Synthesis. New ...
  • Anjaneyulu B., Rao D.G., A Mini Review: Biginelli Reaction for ...
  • Erşatır M., Türk M., Giray E.S., An Efficient and Green ...
  • Hekmatshoar R., Kargar M., Hashemı Z., Golı F., Mostasharı A., ...
  • Oliverio M., Costanzo P., Nardi M., Rivalta I., Procopio A., ...
  • Dallinger D., Kappe C.O., Rapid Preparation of the Mitotic Kinesin ...
  • Villabrille P.I., Palermo V., Sathicq A.G., Vazquez P.G., Romanelli G.P., ...
  • Cheng Q., Et Al. Solvent-Free Synthesis of Monastrol Derivatives Catalyzed ...
  • Dondoni A., Massi A., Sabbatini S., Bertolasi V., Three-Component Biginelli ...
  • Kerr J.F., Wyllie A.H., Currie A.R., Apoptosis: A Basic Biological ...
  • Pachore S.S., Et Al. Successful Utilization of\Upbeta Β-Ketonitrile in Biginelli ...
  • Kantankar A., Rao Y.J., Mallikarjun G., Hemasri Y., Kethiri R.R., ...
  • Sridhar R., Perumal P.T., A New Protocol to Synthesize ۱, ...
  • Xu D.-Z., Li H.,Wang Y., Highly Enantioselective Biginelli Reaction Catalyzed ...
  • Devarajan N., Suresh P., Mil-۱۰۱-So ۳ H Metal–Organic Framework as ...
  • نمایش کامل مراجع