Development of the Commercial Manufacturing Process for Ipatasertib.


Journal

Chimia
ISSN: 0009-4293
Titre abrégé: Chimia (Aarau)
Pays: Switzerland
ID NLM: 0373152

Informations de publication

Date de publication:
25 Aug 2021
Historique:
entrez: 15 9 2021
pubmed: 16 9 2021
medline: 18 9 2021
Statut: ppublish

Résumé

Ipatasertib is a potent small molecule Akt kinase inhibitor currently being tested in Phase III clinical trials for the treatment of metastatic castration-resistant prostate cancer and triple negative metastatic breast cancer. In this paper an overview of the development achievements towards the commercial manufacturing process is given. The convergent synthesis consists of ten steps with eight isolated intermediates and utilizes a wide range of chemical techniques and technologies to build-up this complex drug. All three stereocenters are introduced using enzyme or metal catalysis.

Identifiants

pubmed: 34523401
doi: 10.2533/chimia.2021.605
doi:

Substances chimiques

Piperazines 0
Pyrimidines 0
ipatasertib 524Y3IB4HQ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

605-613

Auteurs

Stephan Bachmann (S)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Hans Iding (H)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Christian Lautz (C)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Isabelle Thomé-Pfeiffer (I)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Caroline Maierhofer (C)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Régis Mondière (R)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Philipp Schmidt (P)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Christoph Strasser (C)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland.

Thomas Bär (T)

Dottikon Exclusive Synthesis AG, Hembrunnstrasse 17, CH-5605 Dottikon, Switzerland.

André Aebi (A)

Dottikon Exclusive Synthesis AG, Hembrunnstrasse 17, CH-5605 Dottikon, Switzerland.

Andreas Schuster (A)

Department of Process Chemistry & Catalysis, Pharma Synthetic Molecules Technical Development, F. Hoffmann-La Roche AG, Grenzacherstrasse 124, CH-4070 Basel, Switzerland;, Email: andreas.schuster.as2@roche.com.

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Classifications MeSH