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连续流动体系中盐酸丙胺卡因的合成

Synthesis of Prilocaine Hydrochloride in Continuous Flow Systems.

作者信息

Sagandira Mellisa B, Sagandira Cloudius R, Watts Paul

机构信息

Nelson Mandela University, PO Box 77000, Port Elizabeth 6031, South Africa.

出版信息

ACS Omega. 2025 Aug 25;10(35):40020-40031. doi: 10.1021/acsomega.5c04742. eCollection 2025 Sep 9.

Abstract

Herein, we showcase how continuous flow technology enables the development of time-efficient, high-yielding synthetic routes for the anesthetic drug prilocaine. Starting from toluene nitration, prilocaine was synthesized in 74% (high-performance liquid chromatography (HPLC)) overall yield with a total residence time of just 13.6 min. Continuous flow technology markedly enhanced the nitration step's selectivity, increasing it from 59% in batch to 79%. The toluidine alkylation step benefited significantly from superheating at 150 °C and enhanced mixing in the flow system, reducing the reaction time from 48 h in batch to merely 4.4 min, affording 98% yield. Additionally, we present streamlined continuous flow reaction, telescoping, and inline workup strategies.

摘要

在此,我们展示了连续流动技术如何为麻醉药物丙胺卡因开发出省时、高产的合成路线。从甲苯硝化开始,丙胺卡因的合成总收率为74%(高效液相色谱(HPLC)),总停留时间仅为13.6分钟。连续流动技术显著提高了硝化步骤的选择性,从间歇反应中的59%提高到了79%。甲苯胺烷基化步骤在150°C的过热条件和流动系统中增强的混合作用下受益匪浅,反应时间从间歇反应中的48小时缩短至仅4.4分钟,收率达到98%。此外,我们还展示了简化的连续流动反应、串联反应和在线后处理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d2/12423797/7aad0b9ba43c/ao5c04742_0001.jpg

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