Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Olopatadine alpha methyl compound and its preparation method and use

A technology of olopatadine and its compound, which is applied in the field of olopatadine α-methyl compound and its preparation, can solve problems such as unfavorable safe production and high safety risk, so as to improve drug safety, improve industry standards, and ensure drug safety Effect

Active Publication Date: 2021-11-02
唯智医药科技(北京)有限公司 +1
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At the same time, because sodium hydride and other materials release flammable gas when they meet water, the safety risk is relatively large in the production process, which is not conducive to safe production. At present, some manufacturers have replaced it with safer bis(trimethylsilyl)amide Sodium (alias: sodium hexamethyldisilazide) or potassium bis(trimethylsilyl)amide is more conducive to safe 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
  • Olopatadine alpha methyl compound and its preparation method and use
  • Olopatadine alpha methyl compound and its preparation method and use
  • Olopatadine alpha methyl compound and its preparation method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Embodiment 1 The method for preparing olopatadine α methyl compound:

[0035]

[0036] Take 20 g of isoket acid (compound 1) and add it to the reaction flask, add 50 ml of isopropanol, stir and cool down to 0-10°C, add 10 g of thionyl chloride dropwise, stir and heat up to reflux after the addition, TLC detects that the reaction is complete After cooling down, thionyl chloride and isopropanol were removed by concentration under reduced pressure, and then 40ml of isopropanol was added for recrystallization to obtain 22g of compound 2.

[0037]

[0038] Take 20g of compound 2, add 200ml of N,N-dimethylformamide, stir and dissolve completely, control the temperature below 10°C, add 8.47g of potassium tert-butoxide, stir and control the temperature below 10°C, add 10.26g of methyl iodide dropwise, and the reaction is complete at room temperature , drop 150ml of purified water to quench the reaction, then use dichloromethane to extract completely, the organic phase is ...

Embodiment 2

[0043] Example 2 Confirmation of impurities

[0044] Multiple batches of the original drug olopatadine hydrochloride (trade name: Alloca) were tested using the following method: mobile phase A was potassium dihydrogen phosphate solution-acetonitrile (75:25), and mobile phase B was potassium dihydrogen phosphate Solution-Acetonitrile (40:60), AgelaVenusil MP C8 (4.6*250mm) chromatographic column, the detection wavelength is 299nm.

[0045] result figure 2 Shown, detect and separate and find the impurity compound of about 0.019% trace (see figure 2 36.682min place), the same separation environment, fully matched with the compound obtained in Example 1. It can be seen that the impurity is the olopatadine α-methyl compound prepared in Example 1.

Embodiment 3

[0047] Preparation system: prepare with reference to the method in CN1042211676:

[0048]

[0049] It is extremely difficult to separate during the separation and preparation of the mother liquor. It exists in a small amount in the mother liquor, and is similar in polarity to other impurities. The peak time in HPLC (high performance liquid chromatography) is relatively close, but it is not easy to prepare and separate. After using more methods for purification and separation (silica gel column chromatography, Sephadex, ODS reverse phase, HPTLC, HPLC, etc.), try to use HPLC for separation, and replace different chromatographic columns (Agela Venusil MP C8 (4.6*250mm), phenomenonex Ultracarb (4.6*150mm, etc.), changing the mobile phase ratio, buffer salt type and ratio, etc., finally found that adding a small amount of trifluoroacetic acid can be effectively separated, and then obtained trace amounts of the Impurities, for structural confirmation.

[0050] Specific process: ...

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 discloses olopatadine α-methyl compound, its preparation method and application, and belongs to the technical field of medicine. The present invention discovers for the first time an impurity compound in the olopatadine medicine—olopatadine alpha methyl compound, and its standard product can be used for qualitative analysis and quantitative detection of the impurity in the olopatadine hydrochloride medicine. At the same time, the present invention also provides a cream based on the compound. The compound can be used as an active component in cream products that mainly treats the main symptoms, and is mainly used for skin diseases such as mosquito bites.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to olopatadine α-methyl compound, its preparation method and application. Background technique [0002] Olopatadine hydrochloride (olopatadine hydrochloride) is an antiallergic drug developed and marketed by Kyowa Hakko, Japan, and has been marketed in Europe, the United States, Japan and other countries. It has the dual functions of inhibiting the release of histamine and selectively antagonizing HI receptors, without the central nervous system depression and cardiotoxic side effects common to HI receptor antagonist antiallergic drugs. It is used orally for allergic rhinitis, skin irritation, polymorphic Treatment of exudative erythema and urticaria. Its eye drops are used to treat allergic conjunctivitis. The drug can not only inhibit the release of histamine from mast cells, but also selectively antagonize H1 receptors, and has no effect on α-adrenoceptors, dopamin...

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): C07D313/12A61K31/335A61P17/00A61K47/06A61K47/14A61K47/18
CPCA61K9/0014A61K9/06A61K47/06A61K47/14A61K47/18A61P17/00A61P17/04C07D313/12
Inventor 瞿鑫方贤罗季子建左伟初野张建楼张佳祥
Owner 唯智医药科技(北京)有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com