EventsThe 20th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session b. Bioorganic, Medicinal and Natural Products Chemistry of the event The 20th International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 2016
Citation
Javad Mokhtari Aliabad, Mehry Hosseini, Issa Yavari, Morteza Rouhani, A very efficient and convenient route for synthesis of imidazol-1-yl-acetic acid: the most important precursor for the synthesis of zoledronic acid, in Proceedings of The 20th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2016, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-20-b013
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A very efficient and convenient route for synthesis of imidazol-1-yl-acetic acid: the most important precursor for the synthesis of zoledronic acid

Mehry Hosseini 1
Issa Yavari 1
Morteza Rouhani 1
1. Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran, Iran
Abstract

Bisphosphonic acids are beneficial antihypercalcemic medicines and could be utilized as remedial factors for the therapy of illnesses which are specified by unusual calcium metabolism.[1] They have showed efficiency in detention bone decline and restituing normocalcemia in patients with metastatic bone disease, hypercalcemia of malignancy, osteoporosis and Paget’s disease and they have the potential for other medical usages as well. In this paper a convenient synthesis of imidazol-1-yl-acetic acid is described. Condensation reaction of a benzyl alcohol and a chloroacetyl chloride in the presence of N,N-diisopropylethylamine gave a benzyl 2-chloroacetate, which on treatment with an imidazole and then a hydrochloric acid afforded the imidazol-1-yl-acetic acid in good yield.

Keywords
Imidazol-1-yl-acetic acid
zoledronic acid
biphosphonic acids
hypercalcemia
drug precursors
Manuscript
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