180 g/批标度制备3-甲基-6-硝基- 1h -茚唑制备帕唑帕尼重要中间体的工艺研究

Văn Hải Nguyễn, Thị Thanh Châm Bùi, Quốc Hùng Phan, Trà Ly Trần, Thị Ngọc Nguyễn, Thị Luyến Bùi, Thu Quỳnh Nguyễn, Nguyệt Sương Huyền Đào, Đình Luyện Nguyễn, Văn Giang Nguyễn
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引用次数: 0

摘要

盐酸帕唑帕尼(Pazopanib hydrochloride)是诺华公司生产的一种抗癌药物,在全球以品牌名Votrient销售。它是目前第一个也是唯一一个被批准用于治疗多种组织学亚型软组织肉瘤(STS)的酪氨酸激酶抑制剂。在之前的研究中,我们提出了在实验室规模上合成3-甲基-5-硝基- 2h -茚唑(3)作为一种重要的茚唑成分(约10 g/批)的初步结果。在本研究中,我们以原料乙胺为原料,以200 g/批的规模成功合成了该化合物(3),总工艺收率为79.6%。该产率高于以往文献报道的产率。改进的技术条件包括:优化硝化反应中硫酸的用量,优化重氮反应中醋酸、氢氧化钠的用量,优化反应温度,优化进料方式,控制反应的安全性,实现200 g/批的高效反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Process of Preparing 3-methyl-6-nitro-1H-indazole by Scale of 180 g/batch as an Important Intermediate for the Preparation of Pazopanib
Pazopanib hydrochloride, marketed worldwide under the brand name Votrient, is an anti-cancer medication manufactured by Novartis. It is the first and only tyrosine kinase inhibitor currently approved for the treatment of multiple histological subtypes of soft tissue sarcoma (STS). In previous studies, we presented initial results regarding the synthesis of 3-methyl-5-nitro-2H-indazole (3) as an important indazole component on a laboratory scale (approximately 10 g/batch). In this study, we have successfully synthesized this compound (3) at a scale of 200 g/batch, achieving an overall process yield of 79.6 % from the starting material ethylaniline. This yield is higher than that reported in previous publications. Some of the technical conditions that have been improved include optimizing the amount of sulfuric acid in the nitration reaction, the amount of acetic acid, sodium hydroxide in the diazotization reaction for ring closure, reaction temperature, and the feed method to control the reaction safely and achieve high efficiency at a scale of 200 g/batch.
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