Iridium-Catalyzed Asymmetric Hydrogenation of Pyridazine Salts under Batch and Flow

Abstract Herein, we report an [Ir(COD)Cl]2/(R)-SunPhos-catalyzed asymmetric hydrogenation of pyridazine salts to construct chiral hexahydropyridazines. The reaction tolerates a wide range of substituents, delivering products in up to 97% yield with 97% ee under mild reaction conditions. Simultaneously, the gram-scale synthesis, continuous-flow operation, and good catalyst turnover (TON up to 3720 with 94% ee at S/C = 4000; TOF up to 155 h–1) further underscored the practicality of this methodology. Collectively, this operationally simple, scalable, and sustainable protocol provides an efficient platform for valuable N-heterocycles featuring chiral hexahydropyridazine cores.

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Publication Details

Journal
Organic Letters
Published
2026-10-13
DOI
https://doi.org/10.1021/acs.orglett.6c03617
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
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article

Iridium-Catalyzed Asymmetric Hydrogenation of Pyridazine Salts under Batch and Flow

Yuxin Lin, Liang Zhi-qian, Fen‐Er Chen, Pei Tang et al.
Organic Letters
Asymmetric Hydrogenation and Catalysis
article

Iridium-Catalyzed Asymmetric Hydrogenation of Pyridazine Salts under Batch and Flow

Yuxin Lin, Liang Zhi-qian, Fen‐Er Chen, Pei Tang, Mengjuan Wu, Hanlin Chen, Yaling Li, Lei Yu
article en

Abstract

Abstract Herein, we report an [Ir(COD)Cl]2/(R)-SunPhos-catalyzed asymmetric hydrogenation of pyridazine salts to construct chiral hexahydropyridazines. The reaction tolerates a wide range of substituents, delivering products in up to 97% yield with 97% ee under mild reaction conditions. Simultaneously, the gram-scale synthesis, continuous-flow operation, and good catalyst turnover (TON up to 3720 with 94% ee at S/C = 4000; TOF up to 155 h–1) further underscored the practicality of this methodology. Collectively, this operationally simple, scalable, and sustainable protocol provides an efficient platform for valuable N-heterocycles featuring chiral hexahydropyridazine cores.

Organic Letters
Sichuan University (CN), Fudan University (CN), Jiangxi Normal University (CN)
Openalex Percentile: Top 28%
Asymmetric Hydrogenation and Catalysis
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