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Vilazodone organic pharmaceutical cocrystal and preparation method thereof

A vilazodone and organic drug technology, applied in the field of vilazodone organic drug co-crystal and preparation thereof

Inactive Publication Date: 2012-10-03
吉林三善恩科技开发有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Drug crystal form research and solid-state characterization of drugs are relatively mature and highly valued fields in the European and American pharmaceutical industry, but they are still in their infancy in the domestic pharmaceutical industry

Method used

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  • Vilazodone organic pharmaceutical cocrystal and preparation method thereof
  • Vilazodone organic pharmaceutical cocrystal and preparation method thereof
  • Vilazodone organic pharmaceutical cocrystal and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Synthesis of organic pharmaceutical co-crystals using vilazodone and saccharin:

[0027] Weighing:

[0028] Reactant vilazodone: saccharin = 1:5 mass ratio feeding. Accurately weigh 5.000 mg and 25.00 mg of vilazodone and saccharin with an analytical balance, and place them in a 25 ml single-necked round bottom flask;

[0029] Dissolution of API:

[0030] Accurately measure 5ml of ethanol with a 5ml pipette, place it in the above-mentioned single-necked round bottom flask, and stir at room temperature.

[0031] Reflux-volatilization heat method:

[0032] Put a magnetic stirrer in the above-mentioned single-mouth round-bottom flask that dissolves the uniform medicine, and set up a reflux device on the single-mouth round-bottom flask. The reflux time is 2 hours, the reflux temperature is 90°C, and the condensate is turned on.

[0033] After reflux, the crude product was filtered, and the filtrate was placed in a 20ml transparent glass vial, covered with tin foil, and pl...

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Abstract

The invention belongs to the field of organic pharmaceutical cocrystal technology and specifically relates to a vilazodone organic pharmaceutical cocrystal and a preparation method thereof. The pharmaceutical cocrystal uses vilazodone as an active component and glucide as a precursor. A basic structural unit of the vilazodone organic pharmaceutical cocrystal comprises four vilazodone molecules and four glucide molecules and a three-dimensional network structure of the vilazodone organic pharmaceutical cocrystal is formed by extending vilazodone molecule and glucide molecule in the direction of X, Y, and Z through hydrogen bond. Space group of the pharmaceutical cocrystal is monoclinic system with axial lengths of a=11.0269-11.1269, b=18.3006-18.4006, c=15.4106-15.4106 and axial angles of alpha=89.950 degrees-90.050 degrees, beta=100.631 degrees-100.731 degrees, gamma=89.950 degrees-90.050 degrees. According to the invention, formation of new crystalline phase of the pharmaceutical cocrystal not only retains the pharmacological properties of the drug but also provides possibilities for further increasing efficacy and bioavailability through modification of physical and chemical properties of the drug such as melting point, stability, solubility, dispersion rate and the like.

Description

technical field [0001] The invention belongs to the technical field of organic drug co-crystals, and in particular relates to a vilazodone organic drug co-crystal and a preparation method thereof. Background technique [0002] In 1894, E. Fischer of Germany proposed the "lock-key" model based on the idea of ​​"selective interaction between molecules", which was the prototype of modern supramolecular science theory. In 1937, German K.L.Wolf et al. created the term "supramolecular" to describe highly ordered entities formed by the association of molecules. In a general sense, any collection of molecules has interactions, so people often refer to them as The structural level of matter aggregation state is called "supramolecular". It was not until 1978 that Professor J.M.Lehn of France finally proposed the complete concept of "supramolecular chemistry" based on the traditional research on the host-guest system rooted in organic chemistry. Supramolecular chemistry is a science ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D405/12C07D275/06
Inventor 张婷赵晓君罗亚楠刘磊韩冰苏红敏贾江涛
Owner 吉林三善恩科技开发有限公司
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