Novel technology for trans-2,6-lupetazin

A technology of dimethylpiperazine and a new process, applied in the field of pharmaceutical intermediates, can solve the problems of high temperature, many inorganic salts, and high reaction temperature, and achieve the effect of high yield

Inactive Publication Date: 2013-08-28
PORSE FINE CHEM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Chinese patent CN101463016A discloses a 1,2-propanediamine as a starting material, and the reaction conditions are copper nitrate, iron nitrate, aluminum oxide, and the high temperature in the water system reaches 300-320 degrees Celsius, and an atmospheric pressure Hydrogen to obtain the product racemate 2,6-dimethylpiperazine, and then separate the cis and trans configurations through a chromatographic column. However, this reaction system has too many inorganic salts, which is not conducive to amplifying the number of reactions; temperature Too high, there is a safety hazard; water as a solvent is not conducive to subsequent processing; only two trans-structure racemates can be obtained, but two absolute configurations of 2S, 6S- and 2R, 6R- cannot be obtained
[0004] Chinese patent CN1634896A discloses that a kind of 3-[(2-aminopropyl)amino]propan-1-o1 is used raw material, and reaction condition is two aluminum oxides, two chromium oxides, iron oxide, copper, ether make solvent and in 260 Celsius, the air pressure is 2MPa, but the raw materials used in this reaction system are uncommon, which is not conducive to industrial production; the reaction system

Method used

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  • Novel technology for trans-2,6-lupetazin

Examples

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Effect test

Embodiment 1

[0028] Using the S-configuration alanine as the starting material, adding di-tert-butyl dicarbonate, and using the two to make the di-tert-butyl dicarbonate carry out amino protection reaction on the S-configuration alanine, thereby Intermediate 2 is generated, and after purification treatment, the purification treatment here is chromatographic column purification, and the purity of intermediate 2 is further obtained to be more than 98%. In this process, the reaction temperature is 25 degrees Celsius, and the reaction time is 24 hours, or the temperature It can be carried out at room temperature instead of high temperature. The chemical reaction formula of this step is:

[0029]

[0030] Here 2 is intermediate 2, S-configuration alanine is left-handed configuration alanine, S means left, that is, counterclockwise rotation.

[0031] Using R-1-amino-2-propanol as a raw material, adding benzaldehyde, and using the two to condense the amino group on the R-1-amino-2-propanol wit...

Embodiment 2

[0043] With R-configuration alanine as starting material, add di-tert-butyl dicarbonate, and make the di-tert-butyl dicarbonate carry out amino protection reaction on the R-configuration alanine, thereby Intermediate 2 is generated, and after purification treatment, the purification treatment here is chromatographic column purification, and the purity of intermediate 2 is further obtained to be more than 98%. In this process, the reaction temperature is 25 degrees Celsius, and the reaction time is 24 hours, or the temperature It can be carried out at room temperature instead of high temperature. The chemical reaction formula of this step is:

[0044]

[0045] Here 2 is intermediate 2, R-configuration alanine is right-handed configuration alanine, R means right, ie clockwise rotation.

[0046] Using S-1-amino-2-propanol as a raw material, add benzaldehyde, and make the amino group on the S-1-amino-2-propanol condense with the carbonyl on the benzaldehyde, And sodium borohyd...

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Abstract

The invention relates to a novel technology for trans-2,6-lupetazin. Chirality substances of S-configuration alanine or R-configuration alanine are adopted, carbonyl imidazole is taken as a condensing agent for preparing dipeptide, walden inversion occurs through a mitsunobu reaction in cyclization so as to obtain a trans-form chirality structure, and then the final product 2S, 6S-lupetazin or 2R, 6R-lupetazin is obtained through reducing by using a reducing agent. Reactions in each step need purification treatment, so that the purity achieves over 98%, and a chemical intermediate of trans 2S, 6S-lupetazin or trans 2R, 6R-lupetazina has pharmaceutical activity and is high in yield.

Description

technical field [0001] The invention relates to the field of pharmaceutical intermediates, more specifically, to a new process of trans-2,6-dimethylpiperazine. Background technique [0002] 2,6-Dimethylpiperazine is an important drug intermediate, and a variety of drugs contain this molecular fragment, such as the psychotropic drug lincazole, the floxacin drugs sparfloxacin and orbifloxacin. It is also widely used in the design of new drugs. For example, the new product JJC-1-059 of Arena Pharmaceutical Company and the new product SU-11925 of SU Biopharmaceutical Company in the Netherlands all introduce this molecular fragment. [0003] Chinese patent CN101463016A discloses a 1,2-propanediamine as a starting material, and the reaction conditions are copper nitrate, iron nitrate, aluminum oxide, and the high temperature in the water system reaches 300-320 degrees Celsius, and an atmospheric pressure Hydrogen to obtain the product racemate 2,6-dimethylpiperazine, and then sep...

Claims

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Application Information

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IPC IPC(8): C07D241/04
Inventor 沈光梓郝忠言王海平王小川欧武交陈卫
Owner PORSE FINE CHEM
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