An alpha-carboline-3-ketone compound and a preparation method thereof

A one-pot synthesis method for α-carboline-3-one compounds was developed by reacting 3-benzylidene-2-p-toluenesulfonyliminoindoline and enaminoketone compounds in the presence of a basic substance. This method overcomes the problems of narrow substrate range, low yield, and harsh reaction conditions in the preparation of α-carboline-3-one compounds in existing technologies, and achieves an efficient and convenient preparation method.

CN122404331APending Publication Date: 2026-07-17ZHEJIANG NORMAL UNIV

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
ZHEJIANG NORMAL UNIV
Filing Date
2026-05-14
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing methods for preparing α-carboline-3-one compounds suffer from problems such as narrow substrate applicability, low yield, harsh reaction conditions, and poor functional group compatibility, lacking efficient and convenient synthetic methods.

Method used

α-Carblin-3-one compounds were prepared by a one-pot reaction in the presence of an alkaline substance using 3-benzylidene-2-p-toluenesulfonyliminoindoline and enaminoketone compounds as raw materials. The reaction conditions were mild and no transition metal catalysis was required.

Benefits of technology

The method achieves the preparation of α-carboline-3-one compounds with high yield and high purity. It is simple to operate, the raw materials are readily available, it has a wide range of applications, and it is suitable for large-scale production.

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Abstract

本发明公开了一种α‑咔啉‑3‑酮类化合物及其制备方法,属于吲哚类衍生物合成技术领域。本发明公开的α‑咔啉‑3‑酮类化合物的制备方法克服了现有技术中底物范围窄、反应条件苛刻、官能团兼容性不佳等不足;制备过程中,本发明以3‑亚苄基‑2‑对甲苯磺酰亚胺基吲哚啉和烯胺酮类化合物为原料,通过一锅法仅需一步反应即可制得。该制备方法具有操作便捷、原料廉价易得、无需过渡金属催化等优点,且官能团兼容性较好,底物适用范围广。依照本发明制备方法得到的产物的产率较高,且通过柱层析分离即可得纯度较高的产品,后处理简便。
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