One-Pot Sequential Synthesis of Pyrido[2,3-d]pyrimidine-Fused Isoxazoles: Regio-and Chemoselectivity in Green Solvent

Abstract A new method has been reported for synthesizing derivatives of isoxazolo[4′,5′:5,6]pyrido[2,3-d]pyrimidine through the reaction of arylglyoxal, 1,3-dimethylbarbituric acid, and 5-aminoisoxazole in water as a green solvent. It involves a one-pot sequential multicomponent reaction, which was carried out in two different approaches (with and without purification of 5-aminoisoxazole). The method forms five chemical bonds and offers advantages such as easy product purification, availability of raw materials, high reaction efficiency, and environmental friendliness. This synthetic strategy has the potential to advance developments in heterocyclic chemistry.

Authors

Publication Details

Journal
Synthesis
Published
2025-05-22
DOI
https://doi.org/10.1055/s-0043-1775493
Citations
2
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
Field-Weighted Citation Impact
1.87
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

One-Pot Sequential Synthesis of Pyrido[2,3-d]pyrimidine-Fused Isoxazoles: Regio-and Chemoselectivity in Green Solvent

Abdolali Alizadeh, Seyed Ali Hosseini
2 citations
Synthesis
Multicomponent Synthesis of Heterocycles
1.87
article

One-Pot Sequential Synthesis of Pyrido[2,3-d]pyrimidine-Fused Isoxazoles: Regio-and Chemoselectivity in Green Solvent

Abdolali Alizadeh, Seyed Ali Hosseini
article en
2 citations

Abstract

Abstract A new method has been reported for synthesizing derivatives of isoxazolo[4′,5′:5,6]pyrido[2,3-d]pyrimidine through the reaction of arylglyoxal, 1,3-dimethylbarbituric acid, and 5-aminoisoxazole in water as a green solvent. It involves a one-pot sequential multicomponent reaction, which was carried out in two different approaches (with and without purification of 5-aminoisoxazole). The method forms five chemical bonds and offers advantages such as easy product purification, availability of raw materials, high reaction efficiency, and environmental friendliness. This synthetic strategy has the potential to advance developments in heterocyclic chemistry.

SynthesisVol. 57(16)
Openalex Percentile: Top 16%
Multicomponent Synthesis of Heterocycles
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.