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Method for synthesizing nucleoside analogue by using continuous flow reactor

A technology of nucleoside analogues and reactors, which is applied in the direction of organic chemistry, can solve problems such as difficult recrystallization and purification processes, complicated temperature control operations, and potential safety hazards, so as to reduce incomplete deprotection of hydroxyl groups and side reactions, and improve reaction efficiency. Efficiency and safety improvement effects

Active Publication Date: 2021-05-04
JIANGSU LONG HEALTHCARE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The temperature control operation is too complicated and cumbersome for operators, and there are potential safety hazards
[0007] (3) The operation process, the post-treatment process is complex, resulting in a certain fluctuation in the yield of the product (65-75%), so there is still a large room for improvement in the yield
In terms of the reaction process, on the one hand, there is an incomplete phenomenon in the removal of the hydroxyl protecting group, and the incomplete removal of the hydroxyl protecting group will produce a series of impurities; on the other hand, one of the by-products, benzyl chloride, is In the quenching operation process, because the quenching time is too long, the substitution of benzyl chloride and the amino group of the nitrogen heterocycle will occur, and N-benzyl substitution impurities will be generated; the impurity types in the above two aspects will be precipitated together with the product; based on Due to the special solubility properties of the product (difficult to dissolve in general organic solvents) and the similarity between the above-mentioned series of impurities and the solubility of the product, it is very difficult to develop a recrystallization purification process, so the purity of the product is still greatly improved space

Method used

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  • Method for synthesizing nucleoside analogue by using continuous flow reactor
  • Method for synthesizing nucleoside analogue by using continuous flow reactor
  • Method for synthesizing nucleoside analogue by using continuous flow reactor

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Embodiment 1

[0041] A continuous flow reactor for the synthesis of (2R, 3R, 4S, 5R)-2-(4-aminopyrrole[1,2-f][1,2,4]triazin-7-yl)-3,4 -The method of dihydroxyl-5-(hydroxymethyl)tetrahydrofuran-2-carbonitrile, the synthetic route is:

[0042] Include the following steps:

[0043] (1) Material preparation: Dissolve about 200g of the raw material in dichloromethane to prepare a 0.5mmol / mL raw material solution, and place it in a raw material solution bottle; 1.0mmol / mL boron trichloride dichloromethane solution (about 1200mL) Directly used as the auxiliary material liquid, placed in the auxiliary material liquid bottle; connect the raw material liquid bottle to the metering pump A; connect the auxiliary material liquid bottle to the metering pump B;

[0044] (2) Reaction temperature parameter setting: start the circulating liquid cooling system, so that the mixer and the main reaction pipeline are at a set temperature of about 5 degrees;

[0045] (3) Material flow rate parameter setting: t...

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Abstract

The invention discloses a method for synthesizing a nucleoside analogue by using a continuous flow reactor. The method comprises the following steps that: a dichloromethane solution of (2R, 3R, 4R, 5R)-2-(4-aminopyrrolo[1, 2-f][1, 2, 4]triazin-7-yl)-3, 4-dibenzyloxy-5-((benzyloxy)methyl)tetrahydrofuran-2-nitrile used as a raw material solution and a dichloromethane solution of boron trichloride used as an auxiliary material solution of a debenzylation reaction respectively enter a mixer through respective pump systems, then flow through a main reaction pipeline, and then enter an aqueous alkali solution for quenching, and filtering and pulping are carried out so as to obtain a target product (2R, 3R, 4S, 5R)-2-(4-aminopyrrolo[1, 2-f][1, 2, 4] triazin-7-yl)-3, 4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-nitrile. The method disclosed by the invention is simple to operate, efficient, high in product yield, high in purity and suitable for large-scale production.

Description

Technical field: [0001] The invention relates to the technical field of organic synthesis, in particular to a method for synthesizing nucleoside analogs using a continuous flow reactor. Background technique: [0002] Compound (2R, 3R, 4S, 5R)-2-(4-aminopyrrole[1,2-f][1,2,4]triazin-7-yl)-3,4-dihydroxy-5-( Hydroxymethyl)tetrahydrofuran-2-carbonitrile is a nucleoside analog, code name GS-441524, which mainly targets viral RNA polymerase and interferes with the process of viral RNA transcription / replication. GS-441524 is phosphorylated into active triphosphate metabolites (NTP structural analogs) by cellular kinases in cells. In viral RNA synthesis, active NTP structural analogs act as competitors of natural nucleoside triphosphates and natural nucleosides (NTP) competes to participate in the transcription / replication of RNA. When the transcription / replication product is inserted into the GS-441524 molecule, the transcription / replication will be terminated prematurely, thereby ...

Claims

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Application Information

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IPC IPC(8): C07D487/04
CPCC07D487/04
Inventor 王怀秋葛敏付明伟李宝成
Owner JIANGSU LONG HEALTHCARE
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