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ChemicalBook CAS DataBase List Etravirine
269055-15-4

Etravirine synthesis

10synthesis methods
Etravirine, also known as TMC 125 and R 165335, is a drug used for the treatment of HIV. Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI). It was also approved in 2008. Etravirine, in combination with other anti-retrovirals, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral treatment-experienced adult patients, who have evidence of viral replication and HIV-1 strains resistant to a non-nucleoside reverse transcriptase inhibitor (NNRTI) and other antiretroviral agents.
Synthetic Routes
  • ROUTE 1
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    Process for the preparation of 4- [6-amino-5-bromo-2- [(4-cyanophenyl) amino]-4-pyrimidinyl]oxy]-3.5-dimethylbe nzonitrile (Etravirine); Rajan, Srinivasan Thirumalai; Eswaraiah, Sajja; Gutta, Madhusudhan; Peri, Seetha Rama Sarma; Assignee MSN Laboratories Private Limited, India; 2016; Patent Information; Apr 21, 2016; WO 2016059646 A2

  • ROUTE 2
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    Ludovici, D. W.; De Corte, B. L.; Kukla, M. J.; Ye, H.; Ho, C. Y.; Lichtenstein, M. A.; Kavash, R. W.; Andries, K.; de Bethune, M.-P.; Azijn, H.; Pauwels, R.; Lewi, P. J.; Heeres, J.; Koymans, L. M. H.; de Jonge, M. R.; Van Aken, K. J. A.; Daeyaert, F. F. D.; Das, K.; Arnold, E.; Janssen, P. A. J.; Bioorganic & Medicinal Chemistry Letters; Volume 11; Issue 17; Pages 2235-2239; Journal; 2001

  • ROUTE 3
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    Fier, Patrick S.; Hartwig, John F.; Journal of the American Chemical Society; Volume 136; Issue 28; Pages 10139-10147; Journal; 2014

  • ROUTE 4
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    Joshi, Shashikant; Maikap, Golak C.; Titirmare, Shyam; Chaudhari, Ashok; Gurjar, Mukund K. An improved synthesis of etravirine. Organic Process Research & Development. Volume 14. Issue 3. Pages 657-660. 2010.

  • ROUTE 5
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    Reddy, Bandi Parthasaradhi; Reddy, Kura Rathnakar; Reddy, Dasari Muralidhara; Reddy, Rapolu Raji; Krishna, Bandi Vamsi; Reddy, Adulla Venkat Narsimha. Preparation of an etravirine intermediate and polymorphs of etravirine. Assignee Hetero Research Foundation, India. WO 2012001695. (2012).

  • ROUTE 6
  • 202112077018966085.jpg

    Hartwig, John; Fier, Patrick. C-H Fluorination of heterocycles with silver (II) fluoride. Assignee University of California, USA. WO 2015013715. (2015).

  • ROUTE 7
  • 202112072763246108.jpg

    Yang, Minmin; Zhou, Xipeng; Wu, Xihan. Method for preparing etravirine and its intermediate. Assignee PharmaBlock (Nanjing) R&D Co., Ltd., Peop. Rep. China. WO 2013178020. (2013).

  • ROUTE 8
  • 202112071007136265.jpg

    Maity, Pintu; Kundu, Debasish; Ghosh, Tubai; Ranu, Brindaban C. Copper catalyzed cyanation through C=C bond cleavage of gem-aryl dibromide followed by second cyanation of iodoarene by a released CN unit. Organic Chemistry Frontiers. Volume 5. Issue 10. Pages 1586-1599. 2018.

  • ROUTE 9
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    Maikap, Golakchandra Sudarshan; Joshi, Shashikant Gangaram; Pardeshi, Devising Rameshsing; Kamble, Mangesh Gorakhanath; Mehta, Samit Satish; Gurjar, Mukund Keshav. Process for synthesis of diarylpyrimidine non-nucleoside reverse transcriptase inhibitor. Assignee Emcure Pharmaceuticals Ltd., India. IN 275560. (2016).

  • ROUTE 10
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    Pullagurla, Manik Reddy; Rangisetty, Jagadeesh Babu; Nandakumar, Mecheril Valsan. Process for the synthesis of etravirine and its intermediates. Assignee Biophore India Pharmaceuticals Pvt. Ltd., India. IN 2012CH04485. (2016).

202112074546249574.jpg

Process for the preparation of 4- [6-amino-5-bromo-2- [(4-cyanophenyl) amino]-4-pyrimidinyl]oxy]-3.5-dimethylbe nzonitrile (Etravirine); Rajan, Srinivasan Thirumalai; Eswaraiah, Sajja; Gutta, Madhusudhan; Peri, Seetha Rama Sarma; Assignee MSN Laboratories Private Limited, India; 2016; Patent Information; Apr 21, 2016; WO 2016059646 A2

269055-76-7 Synthesis
6-Desamino 6-Chloro Etravirine

269055-76-7
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Yield:269055-15-4 40.5%

Reaction Conditions:

in water;

Steps:

A.19 EXAMPLE A19

EXAMPLE A19 4-[[5-bromo4-(4-cyano-2,6-dimethylphenoxy)-6-chloro-2-pyrimidinyl]amino]benzonitrile (0.00250 mol) and NH3/1,4-dioxane 0.5M (0.015 mol) were heated in a pressure vessel at 150° C. for 4 days. The sample was allowed to sit at ambient conditions for 2 days. Water was added slowly to the mixture until a precipitate formed. The mixture was stirred for 2 hours and filtered. The solid was recrystallized from CH3CN to obtain 0.58 g (fraction 1). The filtrate was evaporated (fraction 2). Both fractions were combined and purified by column chromatography, eluding with CH2Cl2. The resulting residue of the desired fraction was recrystallized from CH3CN to yield 0.44 g of 4-[[4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2-pyrimidinyl]amino]benzonitrile (40.5%).

References:

US2003/186990,2003,A1

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