Development of a Scalable Manufacturing Synthesis for Enarodustat

Enarodustat (brand name Enaroy) is an oral hypoxia-inducible factor prolyl hydroxylase (PHD) inhibitor for the treatment of renal anemia in chronic kidney disease (CKD) patients. Establishing a commercial synthetic route for drug substances is essential for ensuring stable delivery to patients. To overcome challenges associated with the medicinal chemistry route, such as avoiding a cryogenic reaction and column purification, we devised a synthetic route incorporating the dichlorotriazolopyridine derivative 14 as a key intermediate, with the regioselective introduction of a phenethyl group onto it as a key step. This key step was resolved through a nucleophilic substitution employing a malonate derivative. We prepared the key intermediate by improving a known reaction which gave extremely low yields. After thorough investigation, we achieved a kilogram-scale synthesis, successfully overcoming these challenges. The overall yield was 23% in 8 chemical steps, with a purity suitable for human administration.

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Publication Details

Journal
Organic Process Research & Development
Published
2025-10-23
DOI
https://doi.org/10.1021/acs.oprd.5c00306
Primary Topic
Additive Manufacturing and 3D Printing Technologies
Type
article
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article

Development of a Scalable Manufacturing Synthesis for Enarodustat

Takashi Yamaguchi, Akira Suma, Kazuyuki Sugimoto, Hiroyuki Abé et al.
Organic Process Research & Development
Additive Manufacturing and 3D Printing Technologies
article

Development of a Scalable Manufacturing Synthesis for Enarodustat

Takashi Yamaguchi, Akira Suma, Kazuyuki Sugimoto, Hiroyuki Abé, Fumito Shimoma, Yosuke Ogoshi, Dai Motoda, Takashi Ito, Takashi Ogo, Takuya Matsui
article en

Abstract

Enarodustat (brand name Enaroy) is an oral hypoxia-inducible factor prolyl hydroxylase (PHD) inhibitor for the treatment of renal anemia in chronic kidney disease (CKD) patients. Establishing a commercial synthetic route for drug substances is essential for ensuring stable delivery to patients. To overcome challenges associated with the medicinal chemistry route, such as avoiding a cryogenic reaction and column purification, we devised a synthetic route incorporating the dichlorotriazolopyridine derivative 14 as a key intermediate, with the regioselective introduction of a phenethyl group onto it as a key step. This key step was resolved through a nucleophilic substitution employing a malonate derivative. We prepared the key intermediate by improving a known reaction which gave extremely low yields. After thorough investigation, we achieved a kilogram-scale synthesis, successfully overcoming these challenges. The overall yield was 23% in 8 chemical steps, with a purity suitable for human administration.

Organic Process Research & DevelopmentVol. 29(11)
Japan Tobacco (Japan) (JP)
Openalex Percentile: Top 66%
Additive Manufacturing and 3D Printing Technologies
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Development of a Scalable Manufacturing Synthesis for Enarodustat — Takashi Yamaguchi, Akira Suma, et al. · Organic Process Research & Development (2025) | TGRS Research Map | TGRS