Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Cis-tetrahydrocarboline intermediate, its synthesis method and its application in the preparation of tadalafil

A technology of tetrahydrocarboline and its synthesis method, which is applied in the field of cis-tetrahydrocarboline intermediate and its synthesis, and the preparation of tadalafil, which can solve the problems of inconvenient purchase and use, and achieve loss avoidance, process stability, and wider use efficiency effect

Active Publication Date: 2017-12-05
湖南千金湘江药业股份有限公司
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] It can be seen that the main synthetic route of synthesizing tadalafil is to take D-tryptophan methyl ester hydrochloride and piperonal as starting materials, through the route of condensation cyclization, acylation, aminolysis cyclization synthesis, through Asymmetric synthesis to construct β-tetrahydrocarboline ring is the key to the whole synthetic route. On the one hand, the Pictet-Spengler (condensation and ring closure) reaction is the most effective and commonly used means to construct β-tetrahydrocarboline ring, but this reaction is easy It leads to the production of cis- and trans-isomers, and usually requires cumbersome treatments such as column chromatography separation or recrystallization to obtain high-purity cis-carboline intermediates. On the other hand, the important raw material piperonal is regulated by the public security department chemicals, it is very inconvenient to buy and use

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
  • Cis-tetrahydrocarboline intermediate, its synthesis method and its application in the preparation of tadalafil
  • Cis-tetrahydrocarboline intermediate, its synthesis method and its application in the preparation of tadalafil
  • Cis-tetrahydrocarboline intermediate, its synthesis method and its application in the preparation of tadalafil

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Add 25.5 g of D-tryptophan methyl ester hydrochloride to the reaction flask, add 150 ml of isopropanol at room temperature, stir, add 1.2 equivalents of 3,4-dihydroxybenzaldehyde, and react at 85°C for 8 hours until the raw material The reaction was basically completed, cooled to room temperature, filtered, and the solid was washed with 50 ml of isopropanol, and then dried in an oven to constant weight. 34.6 g of compound I were obtained with a yield of 92%. The synthetic route map is attached figure 1 shown.

Embodiment 2

[0039] Add 25.5 g of D-tryptophan methyl ester hydrochloride to the reaction flask, add 250 ml of propionitrile at room temperature, stir, add 1.5 equivalents of 3,4-dihydroxybenzaldehyde, and react at 85°C for 16 hours until the raw materials are basically The reaction was completed, cooled to room temperature, filtered, and the solid was washed with 50 ml of isopropanol, and then dried in an oven to constant weight. 34.2 g of compound I were obtained in a yield of 97%. The synthetic route map is attached figure 1 shown.

Embodiment 3

[0041] Add 25.5 g of D-tryptophan methyl ester hydrochloride to the reaction flask, add 375 ml of methanol at room temperature, stir, add 1.5 equivalents of 3,4-dihydroxybenzaldehyde, and react at 60°C for 24 hours until the raw materials are basically reacted Complete, cooled to room temperature, filtered, and the solid was washed with 50 mL of methanol, then dried in an oven to constant weight. 33.8 g of compound I were obtained in a yield of 90%. The synthetic route map is attached figure 1 shown.

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 cis-tetrahydrocarboline intermediate and a synthesis method thereof, and application of the cis-tetrahydrocarboline intermediate in preparing tadalafil. D-tryptophan methyl ester hydrochloride and 3,4-dihydroxybenzaldehyde are used as raw materials to prepare the cis-tetrahydrocarboline intermediate, so that the raw materials are accessible, thereby overcoming the technical defects when the police-controlled precursor chemical heliotropin is used as the raw material in the prior art. The preparation method does not need any catalyst, and can be used for directly preparing the cis-tetrahydrocarboline intermediate by using lower alcohols, nitriles or nitroparaffins as a solvent; and after the reaction finishes, simple cooling and filtration are performed to obtain the product, wherein the mole yield is 90-97%. The cis-tetrahydrocarboline intermediate can be used for preparing tadalafil; and the synthesis method is simple and easy to implement, has the advantages of stable technique and high yield, and is suitable for industrial large-scale production. The structural formula of the cis-tetrahydrocarboline intermediate is disclosed as (I).

Description

technical field [0001] The present invention relates to the technical field of organic synthesis, and more particularly, to a cis-tetrahydrocarboline intermediate, its synthesis method and application in preparing tadalafil. Background technique [0002] Tadalafil is a phosphodiesterase type V (PDE 5) inhibitor originally developed by GlaxoSmithKline (GSK) and approved by the FDA in 2003 as a treatment for erectile dysfunction (ED) in men drugs are available in the United States. Because tadalafil has the advantages of high selectivity, long half-life, greater patient autonomy, and unique pharmacological effects in the clinical treatment of ED, domestic and foreign experts have conducted extensive research on chemical synthesis of tadalafil, and Some results have been achieved. [0003] The synthetic route reported in U.S. Patent No. 5,859,006, this route is to take tryptophan methyl ester and piperonal as raw materials, take dichloromethane as a solvent, and a P-S reactio...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C07D471/04C07D471/14
CPCC07D471/04C07D471/14
Inventor 姚亮元宿亮侯岳华钟爱军袁红波尹军文峰球
Owner 湖南千金湘江药业股份有限公司
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
Eureka Blog
Learn More
PatSnap group products