Synthesis method of toremifene

A synthetic method, the technology of toremifene, applied in chemical instruments and methods, the preparation of organic compounds, the preparation of amino hydroxyl compounds, etc., can solve the problems of poor stereoselectivity and low product synthesis rate, and achieve easy separation and stereoselective High performance and mild reaction conditions

Active Publication Date: 2014-12-24
ASYMCHEM LAB TIANJIN +4
View PDF6 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] The present invention aims to provide a synthetic method of toremifene to solve the problem that the poor ster

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
  • Synthesis method of toremifene
  • Synthesis method of toremifene
  • Synthesis method of toremifene

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0033]In a typical embodiment of the present invention, a synthetic method of toremifene is provided, the synthetic method comprises: Step S1, making the compound B having the structural formula II react with the compound C having the structural formula III in a McMurray reaction , to obtain a compound D having the structural formula IV; Step S2, making the compound D and the compound E having the structural formula V or the hydrochloride of the compound E undergo a selective alkylation reaction on the phenolic hydroxyl group to obtain a compound F having the structural formula VI; Step S3, reacting compound F with thionyl chloride to obtain toremifene, wherein the structural formula II is: Structural formula III is: Structural formula IV is Structural formula Ⅴ is ClCH 2 CH 2 N(CH 3 ) 2 ; Structural formula Ⅵ is

[0034] The synthetic route of above-mentioned synthetic method is as follows:

[0035]

[0036] The above-mentioned synthetic route that the present ...

Embodiment 1

[0050] Synthesis of Z configuration compound D:

[0051] Add 130.8g (2mol) zinc powder and 1.5L THF to the 5L reaction flask, stir evenly to form the first mixed system, control the temperature of the first mixed system to be lower than -15°C, and slowly add 189.7g ( 1mol) of titanium tetrachloride, the dropwise addition is completed, and the second mixed system is formed after continuing to stir for 2 hours; the temperature of the second mixed system is controlled at 20-25°C, and 156.2g (0.8mol) Compound B and 1.5L tetrahydrofuran solution of 150g (1mol) compound C form a third mixed system. After the dropwise addition, the temperature of the third mixed system is raised to 60-65°C. After stirring for 5 hours, the temperature is lowered to 25°C to obtain the first Product system; slowly pour the first product system into 2L of water, add sodium carbonate to neutralize until the pH value of the first product system is between 9 and 10 to obtain the first neutralization system,...

Embodiment 2

[0057] Synthesis of Z configuration compound D:

[0058] Add 294.2g (4.5mol) of zinc powder and 2.25L of ethylene glycol dimethyl ether into a 5L reaction bottle, stir evenly to form the first mixed system, control the temperature of the first mixed system to be lower than -15°C, and slowly transfer to the first mixed system Add 462.6g (3mol) titanium trichloride dropwise to the mixture, after the dropwise addition is complete, continue to stir for 2 hours to form the second mixed system; control the temperature of the second mixed system to be 20-25°C, and slowly add dropwise the second mixed system containing 237.8g (1.2mol) of compound B and 150g (1mol) of compound C in 2.25L ethylene glycol dimethyl ether solution form a third mixed system, after the dropwise addition is completed, the temperature of the third mixed system is raised to 60-65°C, kept stirring for 5 Hours later, cool down to 25°C to obtain the first product system; slowly pour the first product system into 2L ...

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 provides a synthesis method of toremifene. The synthesis method comprises the following steps: S1. performing McMurry reaction to a compound B as shown in a structural formula II and a compound C as shown in a structural formula III, to obtain a compound D as shown in a structural formula IV; S2. performing selective alkylation reaction of phenolic hydroxyl to the compound D and a compound E as shown in a structural formula V or hydrochloride of the compound E, to obtain a compound F as shown in a structural formula VI; and S3. reacting the compound F with thionyl chloride, to obtain the toremifene, wherein the structural formula II, the structural formula III, the structural formula IV, the structural formula V and the structural formula VI are respectively shown in the specification. The obtained compound D has higher stereoselectivity, therefore, the reaction yield of the toremifene with a Z configuration can be increased when the compound D serves as an intermediate to synthesize the toremifene, and the purity of the toremifene with the Z configuration can be improved; and the synthesis method is stable in technology, mild in reaction conditions, the intermediate is easily separated, and the synthesis method can be used for mass production.

Description

technical field [0001] The invention relates to the technical field of pharmaceutical synthesis, in particular to a synthesis method of toremifene. Background technique [0002] Toremifene, the chemical name is (Z)-4-chloro-1,2-diphenyl-1-[4-(2-(N,N-dimethylamino)ethoxy)benzene Base]-1-butene, having structure I. Toremifene is an analogue of Tamoxifen (Tamoxifen), which has anti-estrogen activity and can be used to treat hormone-dependent breast cancer, while its E-type isomer has estrogen activity, and the existence of E-type isomer May counteract the antiestrogenic activity of toremifene, so the isomeric purity of toremifene is critical. Toremifene was developed by Finnish company Famos in 1983. It was launched in the European Union by Orion in 1996 under the trade name of Fareston. It entered my country in 2002 under the trade name of Fareston. [0003] [0004] R.J.Toivola etc. disclose the synthetic route of toremifene in European patent EP95875, U.S. Patent US469...

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): C07C213/08C07C217/18
Inventor 洪浩詹姆斯·盖吉李九远张恩选
Owner ASYMCHEM LAB TIANJIN
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