HFIP-Mediated Multicomponent Reactions: Synthesis of Pyrazole-Linked Thiazole Derivatives
- Riddhiman Banerjee
Riddhiman BanerjeeDepartment of Chemistry, Indian Institute of Technology Patna, Patna 801106, IndiaMore by Riddhiman Banerjee
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- Danish Ali
Danish AliDepartment of Chemistry, Indian Institute of Technology Patna, Patna 801106, IndiaMore by Danish Ali
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- Nurabul Mondal
Nurabul MondalDepartment of Chemistry, Indian Institute of Technology Patna, Patna 801106, IndiaMore by Nurabul Mondal
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- Lokman H. Choudhury*
Lokman H. Choudhury*Email: [email protected], [email protected]Department of Chemistry, Indian Institute of Technology Patna, Patna 801106, IndiaMore by Lokman H. Choudhury
Abstract
The development of one-pot, atom, and step-economic new methods avoiding metal, harsh reaction conditions, and toxic reagents for the synthesis of medicinally important hybrid molecules bearing more than one bioactive moieties is currently one of the hot topics in organic synthesis. Herein, we report a green and efficient room temperature multicomponent reaction for the synthesis of novel pyrazole-linked thiazoles involving a one-pot C–C, C–N, and C–S bond-forming process from the reaction of aryl glyoxal, aryl thioamide, and pyrazolones in 1,1,1,3,3,3-hexafluoroisopropanol, a hydrogen bond donating reaction medium. A set of diverse hybrid molecules bearing thiazole and pyrazole moieties were prepared in good to excellent yields by using this method. This methodology can also be extended to prepare thiazole-linked barbiturates as well as imidazole-linked pyrazoles. All the products were fully characterized by spectroscopic techniques. The notable features of this protocol are room temperature, metal as well as additive-free reaction conditions, use of recyclable solvent, water as the byproduct, wide substrate scope, operational simplicity, easy purification, applicability for gram-scale synthesis, high atom economy, and the presence of two bioactive pyrazole and thiazole moieties in the products.
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