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Atrasentan

Atrasentan. Route Selection by Craig Harris. Objective. To prepare 10 g+ of optically pure Atrasentan to gauge the activity of in-house endothelial antagonists in our tumour models before December 2001.

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Atrasentan

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  1. Atrasentan Route Selection by Craig Harris

  2. Objective • To prepare 10 g+ of optically pureAtrasentan to gauge the activity of in-house endothelial antagonists in our tumour models before December 2001. • Consequence: AZ’s competitor goes into development / dumped and potential licensing agreement with Yamanouchi Pharmaceuticals.

  3. Route Selection • Three publications; official process not registered (still in Phase II) • Abbott’s Asymmetric Route; rather long winded • Abbott’s Racemic Route; much more suited to scale up • Paris Asymmetric Route; large induction much more ameniable to large scale • Why not run both in a staggered fashion?

  4. Abbott’s Asymmetric

  5. Abbott’s Racemic

  6. Abbott Racemic Cont.

  7. Paris Asymmetric

  8. Conclusions • Paris asymmetric route easily best on paper; in practise overall yield was poor (10% chemical yield, 99% e.e.) but can be improved • Paris route provided a very quick way to control Abbott’s Racemic Route ran in parallel (14% chemical yield, 99% e.e.) • Target: Start, 04/08/2001; first submission, 06/09/2001

  9. Combien ça aurait couté?????? • An external reputable contract synthesis; official figure not available but we estimate for 10 g at 100% strength • 1,000,000 FF!!!! • et en Euros? = 152,671

  10. M. Pfau (Paris 5) G. Revial (Paris 5) P. Boutron M. Maudet P. Siret J-C. Arnould G. Pasquet G. Bird C. Delvare D. Dorison T. Boyle (U.K.) D. Roberts (U.K.) Acknowledgements

  11. Grob Pyrrole Formation

  12. Diastereofacial selectivity

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