Nickel-catalyzed hydrogenative coupling of nitriles and amines for general amine synthesis

Author:

Chandrashekhar Vishwas G.ORCID,Baumann WolfgangORCID,Beller Matthias1ORCID,Jagadeesh Rajenahally V.1ORCID

Affiliation:

1. Leibniz-Institut für Katalyse e.V., Albert-Einstein-Str. 29a, D-18059 Rostock, Germany.

Abstract

Efficient and general methods for the synthesis of amines remain in high demand in the chemical industry. Among the many known processes, catalytic hydrogenation is a cost-effective and industrially proven reaction and currently used to produce a wide array of such compounds. We report a homogeneous nickel catalyst for hydrogenative cross coupling of a range of aromatic, heteroaromatic, and aliphatic nitriles with primary and secondary amines or ammonia. This general hydrogenation protocol is showcased by straightforward and highly selective synthesis of >230 functionalized and structurally diverse amines including pharmaceutically relevant and chiral products, as well as 15 N-isotope labeling applications.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference52 articles.

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4. Mordor Intelligence “Amines Market - Growth Trends Covid-19 Impact and Forecasts (2022-2027)” (2022); https://www.mordorintelligence.com/industry-reports/amines-market.

5. Grand View Research “Amines Market Size Share & Trends Analysis Report By Product (Ethanolamines Fatty Amines Alkylamines) By Application (Crop Protection Surfactants Water Treatment) By Region And Segment Forecasts 2018 - 2025” (Report 978-1-68038-291-4 2022); https://www.grandviewresearch.com/industry-analysis/amines-industry.

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