key: cord-0825483-xa22286m
authors: Kumar Palli, Kishore; Ghosh, Palash; Krishna Avula, Shiva; Sridhara Shanmukha Rao, B.; Patil, Amol D.; Ghosh, Subhash; Sudhakar, Gangarajula; Raji Reddy, Chada; Mainkar, Prathama S.; Chandrasekhar, Srivari
title: Total Synthesis of Remdesivir(†)
date: 2021-12-09
journal: Tetrahedron Lett
DOI: 10.1016/j.tetlet.2021.153590
sha: 5570f895fb9ffac7fa0150a3da4cddbb845d4cf1
doc_id: 825483
cord_uid: xa22286m

Remdesivir, the first drug approved by the FDA to treat COVID-19, is in high demand for patients infected with the SARS-CoV-2 virus. Herein, we report a facile approach minimizing the protecting group manipulations to afford remdesivir in good overall yield.

Leave this area blank for abstract info The COVID-19 pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has created a devastating health crisis around the globe. [1] [2] [3] [4] [5] [6] To combat this pandemic, effective and affordable treatments are still being urgently sought. In 2020, the FDA approved remdesivir (1, GS-5734) as the first drug for the treatment of COVID- 19, 7, 8 and subsequently, related molecules such as galidesivir (2), sofosbuvir (3), and molnupiravir (4) were also found to be effective (Fig. 1 ). 9 Remdesivir (1), was initially developed by Gilead Sciences for the treatment of hepatitis C and Ebola virus infections. 10, 11 However, the clinical trials against Ebola were not successful. 12 Remdesivir is a prodrug with good cell permeability and hydrolyzes inside the cell to release a nucleotide triphosphate that targets the key RNA dependent RNA polymerase (RdRp) enzyme responsible for viral replication. The synthetic route developed by Gilead Sciences for the commercial production of remdesivir, 10, 11 involves protecting group manipulations of the sugar part during the synthesis, providing an opportunity for further improvements. Conversion of D-ribose (5) to 2,3,5-tri-O-benzyl-D-ribonolactone (6) followed by addition of modified nucleobase 4-amino-7-iodopyrrolo[2,1f] [1, 2, 4] triazine (7) onto the lactone gave C-glycosylated product 8 in low yield (40%). After cyanation, all three benzyl groups were deprotected using BCl 3 and the two secondary alcohols of the resulting triol were subsequently protected as isopropylidene ketal 10. Finally, introduction of phosphonate ester 11 to ketal 10 followed by hydrolysis of the ketal leads to the target compound remdesivir (1) (Scheme 1). 10 Later, to improve the yield of the Cglycosylation reaction, expensive NdCl 3 was used as an additive in stoichiometric amounts, which improved the yield to 69%. 13, 14 In view of the importance of this being the only FDA-approved drug for COVID-19 mitigation, we reasoned any improvement on the synthetic route would have a large impact on supplies. The opportunities we realized include (a) protecting group manipulations, viz, replacing the benzyl groups with those which could be introduced and removed by catalytic processes avoiding stoichiometric reagents, (b) avoiding the use of NdCl 3 , and (c) achieving anomeric selectivity with better yields. RdRp Remdesivir, the first drug approved by the FDA to treat COVID-19, is in high demand for patients infected with the SARS-CoV-2 virus. Herein, we report a facile approach minimizing the protecting group manipulations to afford remdesivir in good overall yield. We planned our synthesis from D-ribonolactone (12) , which is in the correct oxidation form to introduce the heterocyclic fragment at the anomeric carbon. It was also assumed that a bulky protecting group at the C-5 hydroxyl would enable better selectivity at the anomeric position. Thus, the primary hydroxyl group of commercially available D-ribonolactone (12, can also be synthesized from D-ribose in one step) was silylated with tert-butyldiphenyl silyl (TBDPS) group to afford the corresponding silyl ether 13 in 84% yield. 15 Further protection of the remaining two secondary alcohols using allyl tert-butyl carbonate (14) in the presence of 2 mol% Pd(PPh 3 ) 4 To introduce the desired phosphonate on the primary hydroxyl group, deprotection of the silyl group and Boc group was achieved under HF.pyridine conditions in one-pot to afford aminoalcohol 19 in 89% yield. 19 The next task was to carry out the P-chiral phosphorylation, a key step in the synthesis of remdesivir. 20 Coupling of 19 with the known chiral pentafluoro-phosphoramidate (20) 21 in the presence of t-BuMgCl gave phosphoramidate ester 21 in 86% yield as a single diastereoisomer. Finally, removal of the diallyl groups from 21 was accomplished by Pd-catalyzed reductive deallylation, using a method developed by our group, 22 to obtain the target molecule remdesivir (1) in 91% yield, whose spectral data were in good agreement with the reported data (Scheme 3).

In conclusion, a short synthetic approach to access remdesivir has been developed in seven longest linear steps (LLS) with 25% overall yield starting from D-ribonolactone (12) . The present strategy using a silyl/allyl protected sugar 15 has advantages including (i) avoiding the use of hazardous BCl 3 for benzyl deprotection, (ii) improvement in the coupling yield without any additive, (iii) use of catalytic methods for protection and deprotection of the allyl groups. We believe that the present approach is scalable and can be used for the synthesis of novel analogues in addition to remdesivir as anti-viral agents. 

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. Leave this area blank for abstract info

Current Protocols (2021)

Patent WO2020/247633

We thank the Council of Scientific and Industrial Research (CSIR), Ministry of Science and Technology, Government of India, for research funding (COVID-19 Mission Mode Project, HCP 0029). K.K.P thanks the University Grants Commission (UGC), New Delhi, for a research fellowship. P.G. thanks the CSIR, New Delhi, for a research fellowship. S.C. thanks the Science and Engineering Research Board (SERB), Government of India for the J C Bose fellowship (SB/S2/JCB-002/2015). We also thank Dr. B. Jagadeesh, Head, Centre for NMR, CSIR-IICT, for NMR analytical support.

IICT/Pubs./2021/279.