5-Diazo Dihydrouracils: Preparation and Some Transformations

An approach to a new type of diazo reagents─diazo dihydrouracils─has been developed, and various transformations of the obtained diazo heterocycles have been studied, demonstrating their high synthetic potential for obtaining structurally diverse derivatives based on the privileged dihydrouracil scaffold. The X-H insertion reactions provide high yields of a variety of 5-substituted dihydrouracils. Cyclopropanation and 1,3-dipolar cycloaddition reactions involving a carbonyl ylide intermediate have been carried out to give spiro-annulated derivatives. The limitations of the modification methods with respect to the nature of substituents on the nitrogen atoms of the diazo heterocycle have been outlined.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-09-30
DOI
https://doi.org/10.1021/acs.joc.4c01973
Citations
3
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.75

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article

5-Diazo Dihydrouracils: Preparation and Some Transformations

Alexander Sapegin, Grigory Kantin, Dmitry Dar’in
3 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
0.75
article

5-Diazo Dihydrouracils: Preparation and Some Transformations

Alexander Sapegin, Grigory Kantin, Dmitry Dar’in
article en
3 citations

Abstract

An approach to a new type of diazo reagents─diazo dihydrouracils─has been developed, and various transformations of the obtained diazo heterocycles have been studied, demonstrating their high synthetic potential for obtaining structurally diverse derivatives based on the privileged dihydrouracil scaffold. The X-H insertion reactions provide high yields of a variety of 5-substituted dihydrouracils. Cyclopropanation and 1,3-dipolar cycloaddition reactions involving a carbonyl ylide intermediate have been carried out to give spiro-annulated derivatives. The limitations of the modification methods with respect to the nature of substituents on the nitrogen atoms of the diazo heterocycle have been outlined.

The Journal of Organic ChemistryVol. 89(20)
St Petersburg University (RU), Saint-Petersburg Research Institute of Phthisiopulmonology (RU)
Russian Science Foundation
Zero hunger
Openalex Percentile: Top 32%
Cyclopropane Reaction Mechanisms
0.75
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5-Diazo Dihydrouracils: Preparation and Some Transformations — Alexander Sapegin, Grigory Kantin, et al. · The Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS