A kind of oxidation method for preparing alcatadine

A technology for alcaftadine and intermediates, applied in the field of compound preparation, can solve the problems of unsuitability for industrial scale-up production, polycarboxylic acid impurities, high toxicity, etc., and achieve poor product purity, high total yield, and less impurities Effect

Active Publication Date: 2018-01-12
WUHAN WUYAO SCI & TECH
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Because silver nitrate, selenium dioxide, and ammonium cerium nitrate are more expensive and more toxic, and experiments have found that when these oxidants oxidize alcoholic hydroxyl groups, they will be excessively oxidized to carboxyl groups, resulting in more carboxylic acid impurities
These methods are not suitable for industrial scale-up production

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
  • A kind of oxidation method for preparing alcatadine
  • A kind of oxidation method for preparing alcatadine
  • A kind of oxidation method for preparing alcatadine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Add 30.9g (0.1mol) of AT3, 300mL of dichloromethane, and 150mL of tetrahydrofuran into a 1000mL three-neck flask, stir and dissolve at 10-20°C, add 84.8g (0.2mol) of Dess-Martin reagent, and heat up to 20-20°C after the addition is complete. Continue stirring at 30°C for 1-2 hours, monitor by TLC until the reaction is complete, filter with suction, wash the filtrate once with 100 mL of 10% sodium thiosulfate solution, separate the organic layer, then wash with 100 mL of saturated 5% sodium bicarbonate solution, separate The organic layer was taken out, dried by adding anhydrous sodium sulfate, filtered with suction, and the filtrate was concentrated under reduced pressure. Add 50 mL of isopropanol to the obtained oil and stir, cool down to precipitate a solid, filter and dry to obtain 27.5 g of off-white solid, yield 89.6%. HPLC purity: 98.5%.

Embodiment 2

[0028] Add 30.9g (0.1mol) of AT3, 300mL of dichloromethane, and 150mL of tert-butanol into a 1000mL three-neck flask, stir and dissolve at 10-20°C, add 63.6g (0.15mol) of Dess-Martin reagent, and heat up to Continue stirring at 20-30°C for 1-2 hours, monitor by TLC until the reaction is complete, filter with suction, wash the filtrate once with 100 mL of 10% sodium thiosulfate solution, separate the organic layer, and wash with 100 mL of saturated 5% sodium bicarbonate solution , the organic layer was separated, dried by adding anhydrous sodium sulfate, filtered with suction, and the filtrate was concentrated under reduced pressure. The obtained oil was added with 50 mL of isopropanol and stirred, the temperature was lowered to precipitate a solid, which was filtered and dried to obtain 26.8 g of an off-white solid with a yield of 87.3%. HPLC purity: 98.6%.

Embodiment 3

[0030] Add 30.9g (0.1mol) of AT3, 200mL dichloromethane, and 200mL acetone into a 1000mL three-neck flask, stir and dissolve at 10-20°C, add 84.8g (0.2mol) of Dess-Martin reagent, and heat up to 20-20°C after adding Continue stirring at 30°C for 1-2 hours, monitor by TLC until the reaction is complete, filter with suction, wash the filtrate once with 100 mL of 10% sodium thiosulfate solution, separate the organic layer, then wash with 100 mL of saturated 5% sodium bicarbonate solution, separate The organic layer was taken out, dried by adding anhydrous sodium sulfate, filtered with suction, and the filtrate was concentrated under reduced pressure. The obtained oil was added with 50 mL of isopropanol and stirred, the temperature was lowered to precipitate a solid, and it was filtered and dried to obtain 26.5 g of an off-white solid with a yield of 86.3%. HPLC purity: 98.8%.

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 relates to a novel oxidation method for preparing a histamine H1 receptor antagonist--alcaftadine. The method comprises the step of using a Dess-Martin periodinane as an oxidation reagent to oxidize an intermediate--6,11-dihydro-11-(1-methyl-4-piperidylidene)-5H-imidazo[2,1-b][3]benzazepine-3- methanol so as to obtain the alcaftadine. The novel oxidation method for preparing the alcaftadine is simplified and has the advantages of simple operation, environment-friendly process, cheap and easily-available raw materials and reagents, high yield and more applicability to industrial production.

Description

technical field [0001] The invention relates to a new method for preparing a compound, in particular to a new method for the oxidation reaction of a histamine H1 receptor antagonist—alcaftadine. Background technique [0002] Alcaftadine, trade name: Lastacaft, is a novel histamine H1 receptor antagonist developed by Vistakon Pharmaceuticals. In 2010, it was approved by the FDA for the treatment of itching caused by allergic conjunctivitis, and it was launched in 2010. Lastacaft is now approved for use in pediatric patients over 2 years of age. Alcaftadine is another drug used to treat ocular itching associated with allergic conjunctivitis following Bepreve developed by ISTA Pharmaceuticals. It has a good clinical application prospect. [0003] The oxidation method reported in the patent WO1992022551 about alcaftadine is to convert 6,11-dihydro-11-(1-methyl-4-piperidinylidene)-5H-imidazo[2,1-b][3 ] Benzazepine-3-methanol obtains alcatadine with manganese dioxide oxidation...

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): C07D487/04
CPCC07D487/04
Inventor 朱毅宁东波潘季红杨波陈国华
Owner WUHAN WUYAO SCI & 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