4-(4-氯噻吩-2-基)-5-(4-环己基哌嗪-1-基)噻唑-2-胺的合成方法

By using simple esterification, chlorination, carbonyl dichloroation, and substitution reactions, the complex and costly synthesis process of 4-(4-chlorothiophene-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazole-2-amine in existing technologies has been solved, enabling low-cost industrial production of high-purity products.

CN119569720BActive Publication Date: 2026-07-17SHENZHEN ZHIWEITONG TECH CO LTD

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
SHENZHEN ZHIWEITONG TECH CO LTD
Filing Date
2024-12-03
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing methods for synthesizing 4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazole-2-amine suffer from problems such as long process routes, high production costs, and numerous byproducts that are difficult to purify.

Method used

Using thiophene-2-carboxylic acid as the starting material, the target product is obtained through simple reactions such as esterification, chlorination, carbonyl dichloroation, cyclization, and substitution, using specific catalysts, chlorination reagents, strong bases, and solvents, and controlling the reaction conditions. Finally, the product is purified by recrystallization.

Benefits of technology

It achieves mild reaction conditions, simple operation, few side reactions, low cost, and is suitable for large-scale industrial production, with high product purity.

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Abstract

本发明公开了4‑(4‑氯噻吩‑2‑基)‑5‑(4‑环己基哌嗪‑1‑基)噻唑‑2‑胺的合成方法,属于有机化学合成技术领域,本发明以噻吩‑2‑甲酸为起始原料,经与甲醇成酯、氯代、合成α,α‑二氯代羰基产物、与硫脲关环、与1‑环己基哌嗪取代得到目标产品,避免了现有工艺中存在的羰基化合物α位溴代引起的多溴代副反应,并且一步生成二氯代羰基化合物,减少了工艺步数,降低了纯化难度,反应条件温和、生产操作简单、成本低、安全性高,适合大规模工业化生产。
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