Synthesis of imines via carbonyl-amine condensation in the tricyclic pyrrolo[2,3-d]pyrimidine system

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This is a Experimental Study study.

Rustamkhon Kuryazov

doi:10.59251/2181-3973.2025.v1.138.1.3560

June 1, 2025Deleted Journal

Synthesis of imines via carbonyl-amine condensation in the tricyclic pyrrolo[2,3-d]pyrimidine system

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Key Points

The reaction successfully produced new imines, highlighting the versatility of the pyrrolo[2,3-d]pyrimidine system.
Structures were confirmed using both ¹H-NMR and ¹³C-NMR, providing detailed insight into compound configurations.
This innovative synthetic approach may facilitate the development of novel compounds within the tricyclic chemistry realm.
The inclusion of halogenated phenylamines demonstrates potential diversity in further synthetic applications.

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Implication

This synthesis reports imines from pyrrolo[2,3-d]pyrimidinones with phenylamines, indicating structural insights via NMR analysis.

Abstract

Pyrrolo[2,3-d]pyrimidinones were made by reacting tricyclic pyrrolo[2,3-d]pyrimidinones with 4-halogenated phenylamines. The structures of all the new compounds were figured out using ¹H-NMR, ¹³C-NMR analyses.

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Rustamkhon Kuryazov (2025) studied this question.

synapsesocial.com/papers/68d6cd63b1249cec298b350a https://doi.org/10.59251/2181-3973.2025.v1.138.1.3560

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Synthesis of imines via carbonyl-amine condensation in the tricyclic pyrrolo[2,3-d]pyrimidine system

Key Points

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Implication

Abstract

Discussion

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Synthesis of imines via carbonyl-amine condensation in the tricyclic pyrrolo[2,3-d]pyrimidine system

Key Points

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Implication

Abstract

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