An Efficient and Large Scale Process for Synthesis of Valacyclovir Dr. Reddy's Communication No. IPDO IPM-00156
Corresponding Author(s) : V.V.N.K.V. Prasada Raju
prasadvvnkv@drreddys.com
Asian Journal of Chemistry,
Vol. 22 No. 5 (2010): Vol 22 Issue 5
Abstract
A facile, commercially viable and large scale process is developed for an antiviral drug substance, valacyclovir hydrochloride. Several process related critical factors including organic and heavy metal impurities are efficiently addressed in this process.
Keywords
Antiviral
Valacyclovir
Racemization
D-Isomer
Metal impurities
Resin
Prasada Raju, V., Vedantham, R., D. Khunt, M., T. Mathad, V., K. Dubey, P., & Kalyan Chakravarthy, A. (2010). An Efficient and Large Scale Process for Synthesis of Valacyclovir Dr. Reddy’s Communication No. IPDO IPM-00156. Asian Journal of Chemistry, 22(5), 4092–4098. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/11652
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