Process for the preparation of a pyrrolopyrimidine derivative and intermediates thereof

By optimizing the preparation process of pyrrolopyrimidine derivatives, the selectivity and drug resistance issues of existing FGFR inhibitors have been solved, enabling the efficient and low-cost preparation of high-purity compounds, thus providing a new option for anti-tumor drugs.

CN122145467APending Publication Date: 2026-06-05KANGBAIDA (SICHUAN) BIOTECHNOLOGY CO LTD
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
KANGBAIDA (SICHUAN) BIOTECHNOLOGY CO LTD
Filing Date
2025-12-03
Publication Date
2026-06-05

AI Technical Summary

Technical Problem

Existing FGFR inhibitors suffer from insufficient selectivity and drug resistance in cancer treatment, and also have high toxicity and side effects. There is a need to develop a new generation of FGFR2 and/or FGFR3 inhibitors with high activity and high selectivity.

Method used

A process for preparing pyrrolopyrimidine derivatives is provided, which synthesizes the target compound through a multi-step reaction under different solvent and reagent conditions, including the use of acidic and basic reagents, and optimizes the reaction solvent combination to improve the simplicity of operation, cost-effectiveness and product purity.

Benefits of technology

The preparation of pyrrolopyrimidine derivatives with high yield and high purity has been achieved, making them suitable for industrial production and showing potential application prospects in anti-tumor drugs.

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Abstract

The present application relates to a kind of preparation process of pyrrolopyrimidine derivative or its stereoisomer or tautomer and intermediate thereof, the process is simple, low in cost, reaction yield is high, product purity is high, suitable for industrial production.
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