Process Development of the HCV NS5B Site D Inhibitor MK-8876

Author:

Williams Michael J.1,Chen Qinghao1,Codan Lorenzo2,Dermenjian Renee K.1,Dreher Spencer1,Gibson Andrew W.3,He Xianliang4,Jin Yan1,Keen Stephen P.3,Lee Alfred Y.1,Lieberman David R.3,Lin Wei4,Liu Guiquan4,McLaughlin Mark1,Reibarkh Mikhail1,Scott Jeremy P.3,Strickfuss Sophie3,Tan Lushi1,Varsolona Richard J.1,Wen Feng4

Affiliation:

1. Department of Process Research and Development, Merck Research Laboratories, Rahway, New Jersey 07065, United States

2. Werthenstein BioPharma GmbH (MSD Switzerland), Industrie Nord 1, CH-6105 Schachen, Switzerland

3. Department of Process Chemistry, Merck Sharp & Dohme Ltd., Hertford Road, Hoddesdon, Hertfordshire EN11 9BU, United Kingdom

4. WuXi AppTec Co., Ltd., No. 1 Building, #288 FuTe ZhongLu, WaiGaoQiao Free Trade Zone, Shanghai 200131, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference24 articles.

1. Epidemiology and natural history of HCV infection

2. ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C

3. The global burden of hepatitis C

4. A general approach to substituted 6H-pyrido[2′,3′:5,6] [1,3]oxazino[3,4-a]indole via cyclization from an indoline precursor followed by re-aromatization

5. bMcComas, C. C.; Liverton, N. J.; Habermann, J.; Koch, U.; Narjes, F.; Li, P.; Peng, X.; Soll, R.; Wu, H.; Palani, A.; He, S.; Dai, X.; Liu, H.; Lai, Z.; London, C.; Xiao, D.; Zorn, N.; Nargund, R.Preparation of pyridooxazinoindole derivatives and analogs for use as antiviral agents. WO 2013033971 A1 20130314, 2013.

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