# A general aqueous synthetic strategy towards 1-benzylTHIQs enabled by umpolung hydrazone

**Authors:** Manpreet Kaur, Evan F. W. Chen, Jan Michael Salgado, Ruofei Cheng, Chao-Jun Li

PMC · DOI: 10.1039/d5sc08310a · 2026-01-09

## TL;DR

A new green chemistry method synthesizes 1-benzylTHIQ alkaloids using water and sustainable materials, avoiding hazardous reagents.

## Contribution

A sustainable, aqueous, ruthenium-catalyzed strategy for synthesizing 1-benzylTHIQs with functional group tolerance and minimal waste.

## Key findings

- The method uses renewable aldehydes and water as solvent, avoiding hazardous organometallic reagents.
- A diverse range of substituted 1-benzylTHIQs was synthesized with moderate to excellent yields.
- The approach enables late-stage functionalization of pharmacologically relevant molecules.

## Abstract

Primarily found in plants, 1-benzyltetrahydroisoquinoline (1-benzylTHIQ) alkaloids are a diverse class of N-heterocyclic natural products with biological activity against various infectious diseases and neurodegenerative pathologies. Traditionally, 1-benzylTHIQs are synthesized using commercially inaccessible pre-functionalized materials or hazardous organometallic reagents, making their synthesis challenging. Herein, we developed an environmentally benign synthetic strategy to synthesize 1-benzylTHIQs, which aligns with green chemistry principles. This method utilizes abundant, renewable aldehydes as sustainable alkyl carbanion equivalents, thereby eliminating the use of highly reactive or hazardous organometallic reagents. This reaction is catalyzed by ruthenium, using water as a greener solvent, eliminating the need for organic solvents, thereby reducing its environmental impact. Moreover, only N2 and H2O are produced as by-products, which minimizes waste generation. A diverse array of substituted 1-benzylTHIQs was synthesized, showing good functional group tolerance (without the need to protect the functional groups) and resulting in moderate to excellent yields. The sustainability of our method was further demonstrated through the synthesis of natural 1-benzylTHIQ based alkaloids and late-stage functionalization of pharmacologically relevant molecules.

Ruthenium-catalyzed aqueous umpolung addition of hydrazones provides efficient access to 1-benzylTHIQ scaffolds relevant to natural alkaloid synthesis and drug modification.

## Linked entities

- **Chemicals:** ruthenium (PubChem CID 23950), N2 (PubChem CID 947), H2O (PubChem CID 962)

## Full-text entities

- **Diseases:** neurodegenerative pathologies (MESH:D019636), infectious diseases (MESH:D003141)
- **Chemicals:** ruthenium (MESH:D012428), N2 (MESH:D009584), 1-benzylTHIQ (-), H2O (MESH:D014867), aldehydes (MESH:D000447), alkaloids (MESH:D000470), hydrazone (MESH:D006835)

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12805586/full.md

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Source: https://tomesphere.com/paper/PMC12805586