Method for separating cephalomannine from taxol

A technology of cephalomannine and alkoxy cephalomannine, which is applied in the field of chemical separation to achieve the effects of mild reaction and treatment conditions, convenient separation, high product yield and purity

Active Publication Date: 2011-04-20
无锡紫杉药业股份有限公司
View PDF4 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] The technical problem to be solved in the present invention is to overcome the defects of existing cephalomannine an

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for separating cephalomannine from taxol
  • Method for separating cephalomannine from taxol

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] 100g of cephalomannine and paclitaxel mixture material (containing paclitaxel 9.2%, cephalomannine 61.9% (74mmol) respectively) was dissolved in 0.7L methanol, and 90ml of 1,8-diazabicyclo- Bicyclo(5,4,0)-7-undecene (containing 0.85g, 5.55mmol) in methanol. After stirring for 30 minutes, it was concentrated. After passing through a silica gel column (1.5 kg of silica gel), the gradient elution ratio of the mobile phase ethyl acetate and petroleum ether was gradually increased from 1:1 to 2:1. 37.5 g of paclitaxel was obtained, with a content of 24.1%, and a yield of 98.2%; 62.3 g of 3"-methoxycephalomannine derivatives were obtained, with a purity of 99.8%, and a yield of 98.9%.

Embodiment 2

[0023] Dissolve 100g of cephalomannine and paclitaxel mixture material (respectively containing 7.2% of paclitaxel and 77.3% of cephalomannine (92.9mmol)) in 1.4L of isopropanol, add dropwise 150mL (containing 1.18g, 11.6mmol) A solution of N-methylmorpholine in isopropanol. After stirring for 30 minutes, it was concentrated. After passing through a silica gel column (1.5 kg of silica gel), the gradient elution ratio of the mobile phase ethyl acetate and petroleum ether was gradually increased from 1:1 to 2:1. 22.6 g of paclitaxel was obtained, with a content of 31.3% (8.3 mmol), and a yield of 98.2%; 81.2 g of 3"-isopropoxy cephalomannine derivatives were obtained, with a yield of 98.0%.

Embodiment 3

[0025] Add 100 g of edible activated carbon to 2 liters of concentrated nitric acid, cool with an ice-water bath during the addition, and stir for 20 minutes. Remove the ice bath and use a sonicator instead. After ultrasonic vibration for 10 hours, filter and wash 5 liters of washing filter cake with clear water. Put the filter cake into a vacuum oven and dry it at 60° C. for 24 hours. Then, the dried activated carbon was stored in a sealed metal bottle protected by nitrogen.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a method for separating cephalomannine from taxol, which comprises the following steps: a, performing an 1,4-addition reaction, namely dissolving the mixture of taxol and cephalomannine in short-chain fatty alcohol, adding an organic alkali catalyst and stirring at room temperature; b, concentrating the solution, and performing separation by column chromatography to obtain a cephalomannine derivative and taxol; and c, dissolving the cephalomannine derivative, adding acidified active carbon, heating, refluxing, filtering, concentrating the filtrate, and recrystallizing to obtain cephalomannine. When the separation and purification method disclosed by the invention is used, the raw materials are cheap and readily available, the reaction and treatment conditions are mild, the product yield and purity are high, the separation of cephalomannine from taxol is facilitated considerably, and industrialization can be realized conveniently.

Description

technical field [0001] The invention relates to a chemical separation method, in particular to the separation method of two medicinal components. Background technique [0002] Paclitaxel is a well-known chemotherapeutic drug for the treatment of various metastatic tumors. It has been approved by the U.S. Food and Drug Administration for the treatment of cancers such as ovarian and breast cancer. [0003] Paclitaxel is a natural compound, which was first extracted and isolated from Pacific yew. At present, the main raw materials extracted are European yew, Tibetan yew, Yunnan yew, Chinese yew and southern Chinese yew. Paclitaxel can also be obtained by plant cell suspension culture and mold. [0004] In various raw materials, the concentration of paclitaxel is particularly low, for example, in the bark of Taxus brevifolia, its content is between 0.0004-0.08% (by weight). From raw materials with such low content, it is very difficult to extract and purify compounds for cli...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C07D305/14
Inventor 李隆秦月红冉秀琼黄辉徐信保葛月兰蔡强
Owner 无锡紫杉药业股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap