The University of Liège and Mithra pharmaceuticals are intensifying their collaboration for the production of biosourced estetrol

This research led by the CiTOS Lab at ULiège will enable the development of an innovative process for the production of a key intermediate in the contraceptive product estetrol while reducing the environmental footprint

Peer-Reviewed Publication

UNIVERSITY OF LIEGE

 

IMAGE: COMPUTATIONAL CHEMISTRY AS AN ACCELERATOR FOR THE INTENSIFICATION OF CONTINUOUS FLOW PROCESSES view more 

CREDIT: MICHAËL SCHMITZ, CITOS

Researchers at CiTOS - Center for Integrated Technology and Organic Synthesis of the University of Liège (Belgium) and  Mithra Pharmaceuticals have devised a continuous process for preparing a key intermediate of estetrol. The process is based on a thermolysis reaction feeding upon an estrone sulfoxide derivative. Estrone is a bio-based steroid compound sourced from the soybean industry. This successful collaboration relies on a pioneering approach developed at CiTOS, which features synergy between computational chemistry and intensified continuous flow processes. 

Estetrol is a natural biogenic estrogen derivative with breakthrough potential in hormone-dependent treatments and, in particular, for the oral contraceptive market. Estetrol was approved in 2021 by the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) in combination with drospirenone as an active pharmaceutical ingredient for fifth-generation oral contraceptives. Estetrol is one of the flagship products of Mithra Pharmaceuticals, a pharmaceutical and biotechnology company based in Liège focused on women's health. In view of estetrol’s market expansion, research efforts toward cost-effective and intensified large-scale synthesis were engaged.

Mithra Pharmaceuticals R&D team has teamed up with CiTOS to develop a process towards a key enone intermediate. “Our R&D team has been collaborating for almost three years with Prof. Jean-Christophe Monbaliu under the umbrella of his technology flow platform,” says Amaury Dubart, Industrial Synthesis Associate at Mithra. "We present an applied study relying on a unique methodology, where quantum chemical calculations give an experimental design framework. It allows a priori assessment of the feasibility of a reaction in micro-/ and mesofluidic reactors”, comments Pauline Bianchi, F.R.S- FNRS PhD at CiTOS and lead author of the study. Such a priori benchmarking assessment affords a preselection of reaction conditions and suitable combinations of reagents. It positively impacts the reduction of waste generated during optimization phases. "This last point is a significant improvement to accelerate the development of innovative conditions while minimizing the overall environmental footprint, particularly when compounds with high hormonal activity are at stake", indicates Jean-Christophe Monbaliu.

The collaboration focused on the thermolysis of a key sulfoxide derivative of estrone, which was carefully tailored to minimize by-products and to improve its robustness and productivity. “After optimization, the thermolysis process was transposed into a production pilot, leading to an unprecedented productivity of ~1 kg every three hours. With these metrics transposed to the entire estetrol production scheme, a forecast of several million doses (15 mg formulation) is therefore achievable with a minimal global footprint,” concludes Jean-Christophe Monbaliu.

The successful outcome of this project, funded by the FRS-F.N.R.S. as part of Pauline Bianchi's PhD fellowship, relies on a multidisciplinary approach at the interface between organic chemistry, new process technologies and computational chemistry. This program belongs to one of the priority areas of research at CiTOS, with the ambition of using chemical and technological innovations to accelerate the development of processes with a minimal environmental footprint.

Intensified preparation of a key enone intermediate toward estetrol

CREDIT

Michaël Schmitz, CiTOS

JOURNAL

Reaction Chemistry & Engineering

DOI

10.1039/D3RE00051F 

ARTICLE TITLE

Metal-free synthesis of an estetrol key intermediate under intensified continuous flow conditions