Mapping the dark space of chemical reactions with extended nanomole synthesis and MALDI-TOF MS

Author:

Lin Shishi1ORCID,Dikler Sergei2ORCID,Blincoe William D.3ORCID,Ferguson Ronald D.1ORCID,Sheridan Robert P.4ORCID,Peng Zhengwei4,Conway Donald V.5ORCID,Zawatzky Kerstin3,Wang Heather3ORCID,Cernak Tim6ORCID,Davies Ian W.7ORCID,DiRocco Daniel A.7ORCID,Sheng Huaming3ORCID,Welch Christopher J.3ORCID,Dreher Spencer D.1ORCID

Affiliation:

1. Chemistry Capabilities Accelerating Therapeutics, Merck & Co., Inc., Kenilworth, NJ 07033, USA.

2. Bruker Daltonics, Inc., Billerica, MA 01821, USA.

3. Analytical Research and Development, Merck & Co., Inc., Rahway, NJ 07065, USA.

4. Modeling and Informatics, Merck & Co., Inc., Kenilworth, NJ 07033, USA.

5. Discovery Sample Management, Merck & Co., Inc., Kenilworth, NJ 07033, USA.

6. Discovery Chemistry, Merck & Co., Inc., Boston, MA 02115 USA.

7. Process Research and Development, Merck & Co., Inc., Rahway, NJ 07065, USA.

Abstract

A rapid screen for complex reactants Chemists engaged in reaction discovery tend to report outcomes involving a few, relatively simple reactants. It remains a major challenge to fine-tune reported conditions when the reactants become more structurally complex, as often happens in pharmaceutical research. Lin et al. developed a protocol for rapidly screening different catalytic conditions for C–N coupling across a wide range of complex substrates. The product detection scheme relies on mass spectrometry of nanomole-scale reaction mixtures without any need for intervening chromatography. Science , this issue p. eaar6236

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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