Efficient Synthesis of a Key Intermediate for Moxifloxacin Via Intramolecular Double Stereodifferentiation

Author:

Liao Shouzhu12,Sun Guodong2ORCID,Wu Shuming12,Yang Zaiyou2,Hu Benquan2,Liu Zhuangfeng2,Qin Junhai2,Wang Hailong2,Wang Zhongqing312ORCID

Affiliation:

1. State Key Laboratory of Anti-Infective Drug Development (No. 2015DQ780357), Sunshine Lake Pharma Co., Ltd, Dongguan 523871, P. R. China

2. Department of Process Research and Development, HEC Pharm Group, Dongguan 523871, P. R. China

3. School of Pharmacy, Xiangnan University, Chenzhou 423000, Hunan, P. R. China

Funder

Government of Guangdong Province

State Key Laboratory of Anti-Infective Drug Development

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference36 articles.

1. Antibacterial activity of the fourth-generation fluoroquinolones gatifloxacin and moxifloxacin against ocular pathogens

2. Moxifloxacin

3. IQVIA Inc. 2016. Retrieved 2021-09-17, from IQVIA SMART Global MIDAS Edition database.

4. aPetersen, U.; Krebs, A.; Schenke, T.; Philipps, T.; Grohe, K.; Bremm, K.D.; Endermann, R.; Metzger, K. G.; Haller, I. Quinolone- and Naphthyridone Carboxylic Acid Derivatives as Antibacterial Agents. Patent EP0550903A1, 1993.

5. bRamakrishnan, Ar.; Bhawsar, S.; Narayana, V. Improved Process for The Preparation of (S,S)-2.8-Diazabicyclo[4.3.0]Nonane. Patent WO2009125425A2, 2009.

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