Continuous-Flow Technology for Chemical Rearrangements: A Powerful Tool to Generate Pharmaceutically Relevant Compounds

被引:10
作者
Alfano, Antonella Ilenia [1 ]
Pelliccia, Sveva [1 ]
Rossino, Giacomo [2 ]
Chianese, Orazio [3 ]
Summa, Vincenzo [1 ]
Collina, Simona [2 ]
Brindisi, Margherita [1 ]
机构
[1] Univ Naples Federico II, Dept Pharm DoE 2023 2027, I-80131 Naples, Italy
[2] Univ Pavia, Dept Drug Sci, I-27100 Pavia, Italy
[3] Genetic SpA, I-84084 Fisciano, Italy
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2023年 / 14卷 / 03期
关键词
Curtius rearrangement; Hofmann rearrangement; Schmidt rearrangement; flow chemistry; sustainable synthesis; safety; CHEMISTRY;
D O I
10.1021/acsmedchemlett.3c00010
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The efficacy, safety, and scale-up of several chemical rearrangements remain unsolved problems due to the associated handling of hazardous, toxic, and pollutant chemicals and high-risk intermediates. For many years batch processes have been considered the only possibility to drive these reactions, but continuous-flow technology has emerged, for both academic laboratories and pharmaceutical companies, as a powerful tool for easy, controlled, and safer chemistry protocols, helping to minimize the formation of side products and increase reaction yields. This Technology Note summarizes recently reported chemical rearrangements using continuous-flow approaches, with a focus on Curtius, Hofmann, and Schmidt reactions. Flow protocols, general advantages and safety aspects, and reaction scope for the generation of both privileged scaffolds and active pharmaceutical ingredients will be showcased.
引用
收藏
页码:326 / 337
页数:12
相关论文
共 35 条
  • [1] Flow synthesis approaches to privileged scaffolds - recent routes reviewed for green and sustainable aspects
    Alfano, Antonella Ilenia
    Brindisi, Margherita
    Lange, Heiko
    [J]. GREEN CHEMISTRY, 2021, 23 (06) : 2233 - 2292
  • [2] Azide monoliths as convenient flow reactors for efficient Curtius rearrangement reactions
    Baumann, Marcus
    Baxendale, Ian R.
    Ley, Steven V.
    Nikbin, Nikzad
    Smith, Christopher D.
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2008, 6 (09) : 1587 - 1593
  • [3] A modular flow reactor for performing Curtius rearrangements as a continuous flow process
    Baumann, Marcus
    Baxendale, Ian R.
    Ley, Steven V.
    Nikbin, Nikzad
    Smith, Christopher D.
    Tierney, Jason P.
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2008, 6 (09) : 1577 - 1586
  • [4] Interrupted Curtius Rearrangements of Quaternary Proline Derivatives: A Flow Route to Acyclic Ketones and Unsaturated Pyrrolidines
    Baumann, Marcus
    Moody, Thomas S.
    Smyth, Megan
    Wharry, Scott
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2021, 86 (20) : 14199 - 14206
  • [5] Flow chemistry approaches directed at improving chemical synthesis
    Baxendale, Ian R.
    Brocken, Laurens
    Mallia, Carl J.
    [J]. GREEN PROCESSING AND SYNTHESIS, 2013, 2 (03) : 211 - 230
  • [6] Brown M., 2021, ORG PROCESS RES DEV
  • [7] Technological Innovations in Photochemistry for Organic Synthesis: Flow Chemistry, High-Throughput Experimentation, Scale-up, and Photoelectrochemistry
    Buglioni, Laura
    Raymenants, Fabian
    Slattery, Aidan
    Zondag, Stefan D. A.
    Noel, Timothy
    [J]. CHEMICAL REVIEWS, 2022, 122 (02) : 2752 - 2906
  • [8] Schmidt Reaction of Ketones in DME Solution in a Continuous-Flow Microreactor
    Chen, Yuesu
    Liu, Binjie
    Liu, Xiaofeng
    Yang, Yongtai
    Ling, Yun
    Jia, Yu
    [J]. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2014, 18 (11) : 1589 - 1592
  • [9] Curtius T., 1890, BER DTSCH CHEM GES, V23, P3023, DOI DOI 10.1002/CBER.189002302232
  • [10] Continuous Flow Synthesis of Thieno[2,3-disoquinolin-5(4H)-one Scaffold: A Valuable Source of PARP-1 Inhibitors
    Filipponi, Paolo
    Ostacolo, Carmine
    Novellino, Ettore
    Pellicciari, Roberto
    Gioiello, Antimo
    [J]. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2014, 18 (11) : 1345 - 1353