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Automated radial synthesis of organic molecules

Authors :
Chatterjee, Sourav
Guidi, Mara
Seeberger, Peter H.
Gilmore, Kerry
Source :
Nature. March, 2020, Vol. 579 Issue 7798, p379, 6 p.
Publication Year :
2020

Abstract

Automated synthesis platforms accelerate and simplify the preparation of molecules by removing the physical barriers to organic synthesis. This provides unrestricted access to biopolymers and small molecules via reproducible and directly comparable chemical processes. Current automated multistep syntheses rely on either iterative.sup.1-4 or linear processes.sup.5-9, and require compromises in terms of versatility and the use of equipment. Here we report an approach towards the automated synthesis of small molecules, based on a series of continuous flow modules that are radially arranged around a central switching station. Using this approach, concise volumes can be exposed to any reaction conditions required for a desired transformation. Sequential, non-simultaneous reactions can be combined to perform multistep processes, enabling the use of variable flow rates, reuse of reactors under different conditions, and the storage of intermediates. This fully automated instrument is capable of both linear and convergent syntheses and does not require manual reconfiguration between different processes. The capabilities of this approach are demonstrated by performing optimizations and multistep syntheses of targets, varying concentrations via inline dilutions, exploring several strategies for the multistep synthesis of the anticonvulsant drug rufinamide.sup.10, synthesizing eighteen compounds of two derivative libraries that are prepared using different reaction pathways and chemistries, and using the same reagents to perform metallaphotoredox carbon-nitrogen cross-couplings.sup.11 in a photochemical module--all without instrument reconfiguration. An automated synthesis instrument comprising a series of continuous flow modules that are radially arranged around a central switching station can achieve both linear and convergent syntheses.<br />Author(s): Sourav Chatterjee [sup.1] , Mara Guidi [sup.1] [sup.2] , Peter H. Seeberger [sup.1] [sup.2] , Kerry Gilmore [sup.1] Author Affiliations: (1) Department of Biomolecular Systems, Max-Planck-Institute of Colloids and [...]

Details

Language :
English
ISSN :
00280836
Volume :
579
Issue :
7798
Database :
Gale General OneFile
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
edsgcl.660270493
Full Text :
https://doi.org/10.1038/s41586-020-2083-5