Out-smarting smart drug modafinil through flow chemistry?
Green Chemistry Pub Date: 2022-02-07 DOI: 10.1039/D1GC04666G
Abstract
Modafinil is an anti-narcoleptic drug used to treat excessive daytime sleepiness associated with sleep apnea and shift-work disorder. It is unique in its lack of significant side-effects or addiction-inducing properties and is currently utilized as a superior alternative to other options (e.g., amphetamines). Since the original report of its synthesis in 1976, nearly 20 manuscripts and patents have been published that propose alternative synthetic routes that limit the formation of problematic impurities, reduce the number of steps, or improve the green metrics of the process. Herein we show how the synthesis of modafinil can be improved in a continuous flow setup to deliver modafinil in 77% yield over three steps. No intermediate purification steps are required to obtain an output stream with modafinil in over 80% purity from which USP-grade modafinil can be isolated by precipitation, filtration and washing with solvent. The synthesis, performed entirely in class 3 FDA solvents, has a lower E-factor than current industrial processes and results entirely in innocuous side products (NaCl, NaHSO4). Finally, the process can be conducted in a single concatenated flow setup and is the first step in our efforts towards constructing an end-to-end pharmaceutical manufacturing system.
Recommended Literature
- [1] Emerging investigators Polym. Chem., 2015,6, 5501-5502 10.1039/C5PY90111A
- [2] Esterase-responsive polymeric prodrug-based tumor targeting nanoparticles for improved anti-tumor performance against colon cancer? Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun CaoRSC Adv., 2016,6, 42109-42119 10.1039/C6RA05236C
- [3] Evolution of cellulose into flexible conductive green electronics: a smart strategy to fabricate sustainable electrodes for supercapacitors Tengfei Yu,Yuehan Wu,Wei Li,Bin LiRSC Adv., 2014,4, 34134-34143 10.1039/C4RA07017H
- [4] Enantiomorphic symmetry breaking in crystallization of molten sodium chlorate? Martin R. Ward,Gary W. Copeland,Andrew J. AlexanderChem. Commun., 2010,46, 7634-7636 10.1039/C0CC02563A
- [5] Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals? Shojiro Kimura,Tetsuro KusamotoChem. Commun., 2020,56, 11195-11198 10.1039/D0CC04830E
- [6] Distinct roles of SNARE-mimicking lipopeptides during initial steps of membrane fusion? Alena Koukalová,?árka Pokorná,Aimee L. Boyle,Nestor Lopez Mora,Alexander Kros,Martin Hof,Radek ?achlNanoscale, 2018,10, 19064-19073 10.1039/C8NR05730C
- [7] Excellent peroxidase mimicking property of CuO/Pt nanocomposites and their application as an ascorbic acid sensor? Xinhuan Wang,Shuangfei Cai,Cui QiAnalyst, 2017,142, 2500-2506 10.1039/C7AN00589J
- [8] Embedding cyclic nitrone in mesoporous silica particles for EPR spin trapping of superoxide and other radicals? Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael HardyAnalyst, 2019,144, 4194-4203 10.1039/C9AN00468H
- [9] Excitable dynamics in the bromate–sulfite–ferrocyanide reaction J. Zagora,M. Vosla?,L. Schreiberová,I. SchreiberPhys. Chem. Chem. Phys., 2002,4, 1284-1291 10.1039/B110048C
- [10] EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis? Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” KimLab Chip, 2009,9, 1732-1739 10.1039/B821508A
Journal Name:Green Chemistry
research_products
-
CAS no.: 89640-58-4