New Method for Asymmetric N,N-Acetal Synthesis Promises Advances in Drug Development (Chemistry)

A lot of our medicines and other bioactive drugs are based on chemical structures called “enantiomers”ー molecules that are mirror images of each other and are non-superimposable. Notable among them are chiral N,N-acetals contained in diuretic drugs like bendroflumethiazide and thiabutazide, used to treat high blood pressure and edema. Because an enantiomer and its mirror image version often have different biological activities, with only one of them having pharmacological utility, an “enantioselective” or asymmetric synthesis yielding the desired enantiomer in greater amounts is highly desirable.

In the case of N,N-acetals, several studies have demonstrated their enantioselective preparation from aldehydes, aldimines, or enamines. However, in all these cases, their reaction partner has been limited to aldehyde or imines. While ketones have been employed, with instances of successful enantioselective N,N-acetal synthesis, their useーin generalーis not considered effective.

In a recent study published in Advanced Synthesis & Catalysis, scientists from Nagoya Institute of Technology (NITech) and Osaka University in Japan explored this situation with an enantioselective synthesis of chiral N,N-acetals from α-dicarbonyl compoundsーcompounds with two carbonyl (ketone) groups on the α-carbonーin presence of chiral imidazoline phosphoric acid catalysts, and obtained yields as high as 99% with a maximum enantiopurity of 96%.

“Our study presents the first highly stereoselective formation of chiral N,N-acetals from α-ketoesters using an original catalyst that can be used for other stereoselective synthetic reactions as well,” says Prof. Shuichi Nakamura from NITech, who led the study.

The scientists began by examining the reaction of 2-aminobenzamide with various α-ketoesters in presence of different catalysts. The α-ketoesters differed from one another in the nature of the functional group attached to the α-carbon, while the catalysts chosen were bis(imidazoline)-phosphoric acid with different substituents attached to the nitrogen in the imidazoline ring, mono-imidazoline-phosphoric acid, and two commercial chiral phosphoric acids. Among these various combinations, scientists found the best yield (99%) and enantiopurity (92%) in the case of α-ketoester with benzhydryl group and a bis(imidazoline)-phosphoric acid catalyst with 1-naphthalenesulfonyl group.

Scientists next examined the reaction of various aminobenzamides (bearing either an electron-donating methyl group or electron-withdrawing fluoro, chloro, and bromo groups) with different α-ketoesters (containing the same benzhydryl group but different functional groups in place of an earlier phenyl group) keeping the same bis(imidazoline)-phosphoric acid catalyst with 1-naphthalenesulfonyl group. All the combinations showed good yield (77-95%) along with high enantioselectivity (82-96%).

In addition, the team looked at the enantioselective synthesis of N,N-acetals via the reaction of N-benzyl isatin (a cyclic α-ketoamide), benzil (an acyclic diketone), and benzaldehyde with 2-aminobenzamide for the same catalyst. All three reactions yielded products with high enantiopurity (91-93%).

The team also proposed a possible mechanism for the N,N-acetal formation reaction corresponding to the best yield (99%), involving a ketimine intermediate with an amide group that helps avoid steric repulsion between the phenyl group on imidazoline, enabling the formation of an (R)-isomer with high enantiopurity.

While the mechanism is still speculative and requires further investigationscientists are excited about the potential implications of the experimental results. “Our new method will enable the synthesis of candidate pharmaceutical drugs that are currently difficult to synthesize, and can even potentially help create and provide people with new and better medicines in the future,” concludes Prof. Nakamura.

Now, those are some promising consequences to look forward to!

This study was supported by the Takahashi Industrial and Economic Research Foundation and the Astellas Foundation for Research on Metabolic Disorders.

Featured image: A possible mechanism for the formation of chiral N,N-acetal via reaction between 2-aminobenzamide and α-ketoester in presence of chiral bis(imidazoline)-phosphoric acid catalyst. Picture courtesy: Shuichi Nakamura from NITech


Reference: Shuichi Nakamura, Tatsumi Wada, Tsunayoshi Takehara, Takeyuki Suzuki, “Catalytic Enantioselective Synthesis of N,N‐Acetals from α‐Dicarbonyl Compounds Using Chiral Imidazoline‐Phosphoric Acid Catalysts”, Adv. Synth. Catal. 2020, 362, 5374. https://doi.org/10.1002/adsc.202001128 https://onlinelibrary.wiley.com/doi/10.1002/adsc.202001128


Provided by Nagoya Institute of technology

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