Method for preparing key intermediate of Remdesivir by using micro-channel reaction device

A channel reaction device and a technology for microchannel reaction, which are applied in the preparation of sugar derivatives, chemical instruments and methods, chemical/physical/physical-chemical reactors, etc., and can solve the problems of difficult industrial amplification, harsh reaction conditions, and low reaction efficiency. , to achieve the effect of good material mixing effect, simple operation and avoidance of reaction conditions

Active Publication Date: 2020-08-04
NANJING UNIV OF TECH
View PDF2 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Purpose of the invention: The technical problem to be solved by the present invention is to address the deficiencies of the prior art, and to provide a method for preparing the key intermediate (3R, 4R, 5R)-2-(4-aminopyrrolo) of Remdesivir using a microchannel reaction device. [2,1-f][1,2,4]triazin-7-yl)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol method to solve the problems of harsh reaction conditions, low reaction efficiency, and difficulty in industrial scale-up in the prior art

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
  • Method for preparing key intermediate of Remdesivir by using micro-channel reaction device
  • Method for preparing key intermediate of Remdesivir by using micro-channel reaction device
  • Method for preparing key intermediate of Remdesivir by using micro-channel reaction device

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] This example provides a method for preparing the key intermediate of remdesivir (3R,4R,5R)-2-(4-aminopyrrolo[2,1-f][1,2,4] using a microchannel reaction device Triazin-7-yl)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol, such as figure 1Shown, concrete synthesis method comprises the following steps:

[0039] Weigh 5.20g (20mmol, 1.0equiv) of 7-iodopyrrolo[2,1-f][1,2,4]triazin-4-amine, fully dissolve in tetrahydrofuran solvent, and add 5.0mL TMS-Cl (40mmol, 2.0equiv), prepared into 100mL solution, as material Ⅰ; measure PhMgCl 2 (2M, 40mmol, 2.0equiv) tetrahydrofuran solution 20mL and 20mL i PrMgCl 2 LiCl (1M, 20mmol, 1.0equiv) was mixed with THF solution as material II; 8.36g (20mmol, 1.0 equiv), fully dissolved in tetrahydrofuran solvent, prepared into 50mL solution, as material III. Simultaneously pump material I and material II, wherein, material I is pumped at a flow rate of 2.5 mL / min, and material II is pumped at a flow rate of 1.0 mL / min. Aft...

Embodiment 2

[0041] This example provides a method for preparing the key intermediate of Remdesivir (3R, 4R, 5R)-2-(4-aminopyrrolo[2,1-f][1,2,4] using a microchannel reaction device Triazin-7-yl)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol, such as figure 1 Shown, concrete synthesis method comprises the following steps:

[0042] Weigh 5.20g (20mmol, 1.0equiv) of 7-iodopyrrolo[2,1-f][1,2,4]triazin-4-amine, fully dissolve it in tetrahydrofuran solvent, and add 5.0mL TMS-Cl (40mmol, 2.0equiv), prepared into 80mL solution, as material Ⅰ; measure PhMgCl 2 (2M, 40mmol, 2.0equiv) tetrahydrofuran solution 20mL and 20mL i PrMgCl 2 LiCl (1M, 20mmol, 1.0equiv) was mixed with tetrahydrofuran solution as material II; 8.36g (20mmol, 1.0 equiv), fully dissolved in tetrahydrofuran solvent, prepared into 50mL solution, as material III. Simultaneously pump material Ⅰ and material Ⅱ, wherein, the pumping flow rate of material Ⅰ is 2.5 mL / min, and the pumping flow rate of material Ⅱ is 1...

Embodiment 3

[0044] This example provides a method for preparing the key intermediate of remdesivir (3R,4R,5R)-2-(4-aminopyrrolo[2,1-f][1,2,4] using a microchannel reaction device Triazin-7-yl)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol, such as figure 1 Shown, concrete synthesis method comprises the following steps:

[0045] Weigh 5.20g (20mmol, 1.0equiv) of 7-iodopyrrolo[2,1-f][1,2,4]triazin-4-amine, fully dissolve it in tetrahydrofuran solvent, and add 5.0mL TMS-Cl (40mmol, 2.0equiv), prepared into 50mL solution, as material Ⅰ; measure PhMgCl 2 (2M, 40mmol, 2.0equiv) tetrahydrofuran solution 20mL and 20mL i PrMgCl 2 LiCl (1M, 20mmol, 1.0equiv) was mixed with tetrahydrofuran solution as material II; 8.36g (20mmol, 1.0 equiv), fully dissolved in tetrahydrofuran solvent, prepared into 50mL solution, as material III. Simultaneously pump material I and material II, wherein, material I is pumped at a flow rate of 2.5 mL / min, and material II is pumped at a flow rate of 2...

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

PropertyMeasurementUnit
lengthaaaaaaaaaa
Login to view more

Abstract

The invention discloses a method for preparing a Remdesivir key intermediate by using a micro-channel reaction device, comprising the following steps of: (1) adding 7-iodopyrrolo [2, 1-f] [1, 2, 4] triazine-4-amine into an organic solvent, and adding trimethylchlorosilane to obtain a mixed solution as a first material; taking an organic mixed solution of phenyl magnesium chloride and isopropyl magnesium chloride. magnesium chloride as a second material; adding 2, 3, 5-tri-O-benzyl-D-ribose-1, 4-lactone into an organic solvent to be used as a third material; (2) respectively pumping the first material and the second material into a first micro-mixer of a micro-channel reaction device at the same time, mixing, and introducing into the first micro-reactor for reaction; and (3) pumping an effluent of the first micro-reactor and the third material into a second micro-mixer of the micro-channel reaction device at the same time, mixing, introducing into the second micro-reactor for reaction,and collecting an effluent, thereby obtaining the product.

Description

technical field [0001] The invention belongs to the field of chemical synthesis, and specifically relates to a method for preparing the key intermediate (3R, 4R, 5R)-2-(4-aminopyrrolo[2,1-f][1, 2,4] Triazin-7-yl)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol method. Background technique [0002] After a large number of screenings and preliminary clinical experiments, scientific research teams at home and abroad have proved that a batch of existing antiviral drugs such as favipiravir, chloroquine phosphate, remdesivir, etc. can play a positive role in the treatment of new coronary pneumonia. As a drug with the most potential for the treatment of new coronary pneumonia, decivir has received great attention. [0003] Remdesivir, the chemical name is (2S)-2-ethylbutyl2-(((S)-(((2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1f][1 ,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(phenoxy)phosphoryl)amino)propanoate, CAS No.: 1809249-37-3, is a Nucleotide a...

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 Applications(China)
IPC IPC(8): C07H15/18C07H1/00B01J19/00
CPCB01J19/0093C07H1/00C07H15/18
Inventor 郭凯覃龙州邱江凯袁鑫崔玉声庄恺强陈琳孙蕲段秀
Owner NANJING UNIV OF TECH
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