Continuous Flow Synthesis of Nitrofuran Pharmaceuticals Using Acetyl Nitrate

H Hubert Hellwig (Center for Integrated Technology and Organic Synthesis (CiTOS) MolSys Research Unit, University of Liège B6a, Room 3/19, Allée du Six Août 13 Liège (Sart Tilman) B‐4000 Belgium) L Loïc Bovy (Center for Integrated Technology and Organic Synthesis (CiTOS) MolSys Research Unit, University of Liège B6a, Room 3/19, Allée du Six Août 13 Liège (Sart Tilman) B‐4000 Belgium) K Kristof Van Hecke (XStruct, Department of Chemistry, Ghent University, Krijgslaan 281-S3, B-9000 Ghent, Belgium) C Cornelis P. Vlaar (Department of Pharmaceutical Sciences University of Puerto Rico–Medical Sciences Campus San Juan PR 00936 USA) R Rodolfo J. Romañach (Department of Chemistry University of Puerto Rico – Mayagüez Mayagüez PR 00681 USA) M Md. Noor‐E‐Alam (Department of Mechanical and Industrial Engineering College of Engineering, Center for Health Policy and Healthcare Research, Northeastern University Boston MA 02115 USA) A Allan S. Myerson (Department of Chemical Engineering Massachusetts Institute of Technology Cambridge MA 02139 USA) T Torsten Stelzer (Department of Pharmaceutical Sciences University of Puerto Rico–Medical Sciences Campus San Juan PR 00936 USA) J Jean‐Christophe M. Monbaliu (Center for Integrated Technology and Organic Synthesis (CiTOS) MolSys Research Unit, University of Liège B6a, Room 3/19, Allée du Six Août 13 Liège (Sart Tilman) B‐4000 Belgium)

Abstract

Abstract Nitrofurfural is a key building block for the synthesis of antimicrobial nitrofurans as active pharmaceutical ingredients. Its synthesis involves the nitration of furfural, a substrate derived from biobased resources. However, furfural has a delicate heteroaromatic backbone. Typical nitrations involve harsh reaction conditions, which often compromise this structure, resulting in poor reproducibility and low yields. Although acetyl nitrate, a mild nitrating agent, is suitable for this task, major deterrents remain. First, its conventional preparation method involves conditions that are not compatible with furfural. Second, significant safety concerns are associated with the unstable and explosive nature of acetyl nitrate. These critical issues are addressed herein. A safe and robust continuous flow platform featuring in situ generation of acetyl nitrate for the nitration of furfural to nitrofurfural is reported. The high level of integration and automation enables remote process operation by a single operator. Key furfural‐based pharmaceutical intermediates were synthesized with favorable metrics and high reproducibility. The efficiency of this flow platform is demonstrated using a selection of best‐selling nitrofuran pharmaceuticals (nifuroxazide, nifurtimox, nitrofurantoin, and nitrofural), which were obtained with excellent isolated yields in under five minutes.

Article Details

Volume / Issue Vol. 64, Issue 25
Published June 17, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

H

Hubert Hellwig

Center for Integrated Technology and Organic Synthesis (CiTOS) MolSys Research Unit, University of Liège B6a, Room 3/19, Allée du Six Août 13 Liège (Sart Tilman) B‐4000 Belgium

L

Loïc Bovy

Center for Integrated Technology and Organic Synthesis (CiTOS) MolSys Research Unit, University of Liège B6a, Room 3/19, Allée du Six Août 13 Liège (Sart Tilman) B‐4000 Belgium

K

Kristof Van Hecke

XStruct, Department of Chemistry, Ghent University, Krijgslaan 281-S3, B-9000 Ghent, Belgium

C

Cornelis P. Vlaar

Department of Pharmaceutical Sciences University of Puerto Rico–Medical Sciences Campus San Juan PR 00936 USA

R

Rodolfo J. Romañach

Department of Chemistry University of Puerto Rico – Mayagüez Mayagüez PR 00681 USA

M

Md. Noor‐E‐Alam

Department of Mechanical and Industrial Engineering College of Engineering, Center for Health Policy and Healthcare Research, Northeastern University Boston MA 02115 USA

A

Allan S. Myerson

Department of Chemical Engineering Massachusetts Institute of Technology Cambridge MA 02139 USA

T

Torsten Stelzer

Department of Pharmaceutical Sciences University of Puerto Rico–Medical Sciences Campus San Juan PR 00936 USA

J

Jean‐Christophe M. Monbaliu

Center for Integrated Technology and Organic Synthesis (CiTOS) MolSys Research Unit, University of Liège B6a, Room 3/19, Allée du Six Août 13 Liège (Sart Tilman) B‐4000 Belgium