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

A kind of synthetic method of pholcodine

A synthesis method and a pholcodine technology, applied in organic chemistry methods, organic chemistry and other directions, can solve the problems of reduced difficulty and safety risk, increased production operations, and many reaction steps, and achieves improved overall yield, quality, and reaction. Step-by-step effect

Active Publication Date: 2020-05-26
YICHANG HUMANWELL PHARMA
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] This method uses more highly toxic and highly corrosive reagents, and the repeated use of strong acid and strong alkali reagents in large quantities. Most of the organic solvents used are flammable and explosive solvents and the required amount is relatively large. The condensation reaction process requires higher conditions. , it is easy to generate elimination products, and the overall reaction steps are more difficult for the generation operation and bring safety risks, which reduces the yield of the final product

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 synthetic method of pholcodine
  • A kind of synthetic method of pholcodine
  • A kind of synthetic method of pholcodine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] 1) 285.3g morphine base is dissolved in the DMF solution of 2000ml.

[0049] 2) Dissolve 282g of 1,2-dibromoethane in 800ml of DMF solution and add 110g of anhydrous sodium carbonate. Under nitrogen protection, the temperature was raised to 60° C., and the DMF solution of morphine base prepared in 1) was slowly dropped into the 1,2-dibromoethane solution under stirring. After the dropwise addition was completed, the insulation reaction was continued for 2 hours.

[0050] 3) After the reaction is complete, distill under reduced pressure until there is no liquid drop, add 550ml of purified water and stir to dissolve the inorganic salt. The insoluble matter was collected by filtration and dried.

[0051] 4) 105g morpholine and 3) insolubles are dissolved in 2000ml DMF, and add 110g anhydrous sodium carbonate and 10g nano CuI powder. Under the protection of nitrogen, the temperature was raised to 115° C. for 6 hours.

[0052] 5) Suction filtration while hot, collect the...

Embodiment 2

[0064] 1) 285.3g morphine base is dissolved in the DMF solution of 2000ml.

[0065] 2) Dissolve 423g of 1,2-diiodoethane in 800ml of DMF solution and add 110g of anhydrous sodium carbonate. Under nitrogen protection, the temperature was raised to 60° C., and the DMF solution of morphine base prepared in 1) was slowly dropped into the 1,2-diiodoethane solution under stirring. After the dropwise addition was completed, the insulation reaction was continued for 2 hours.

[0066] 3) After the reaction is complete, distill under reduced pressure until there is no liquid drop, add 550ml of purified water and stir to dissolve the inorganic salt. The insoluble matter was collected by filtration and dried.

[0067] 4) 105g morpholine and 3) insolubles are dissolved in 2000ml DMF, and add 110g anhydrous sodium carbonate and 10g nano CuI powder. Under the protection of nitrogen, the temperature was raised to 115° C. for 8 hours.

[0068] 5) Suction filtration while it is hot, collect...

Embodiment 3

[0078] 1) Dissolve 285.3g of morphine base in 2000ml of DMSO solution.

[0079] 2) Dissolve 282g of 1,2-dibromoethane in 800ml of DMSO solution and add 140g of anhydrous potassium carbonate. Under nitrogen protection, the temperature was raised to 60° C., and the DMF solution of morphine base prepared in 1) was slowly dropped into the 1,2-dibromoethane solution under stirring. After the dropwise addition was completed, the insulation reaction was continued for 2 hours.

[0080] 3) After the reaction is complete, distill under reduced pressure until there is no liquid drop, add 550ml of purified water and stir to dissolve the inorganic salt. The insoluble matter was collected by filtration and dried.

[0081] 4) 105g morpholine and 3) insolubles are dissolved in 2000ml DMSO, and 140g anhydrous potassium carbonate and 10g nano CuI powder are added. Under the protection of nitrogen, the temperature was raised to 120° C. for 7 hours.

[0082] 5) Suction filtration while hot, c...

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 a synthetic method of pholcodine. The synthetic method of pholcodine comprises the steps of deriving a phenolic hydroxyl group of a morphine base as a starting material to prolong the branch, then reacting the intermediate with an amine group on morpholine to generate crude pholcodine, and refining the crude pholcodine by means of purification to obtain pholcodine. The method is simple in reaction steps and economical and readily available in reagents, avoids the risk of using a large amount of highly toxic, flammable and explosive solvents, and greatly improves the yield and purity of the product.

Description

technical field [0001] The invention relates to the field of compound drug synthesis, in particular to a synthesis method of pholcodine. Background technique [0002] Pholcodine, also known as morphine or pholcodine, is a semi-synthetic derivative of morphine. It is a central antitussive suppressant with sedative and analgesic effects, similar to codeine, but its oral antitussive effect is stronger than codeine, its addiction is weaker, and its respiratory depression effect is smaller than that of morphine. For the treatment of severe dry cough and moderate pain, newborns and children are easy to tolerate this drug, and will not cause constipation and digestive disorders. The structural formula is as follows: [0003] [0004] There are not many synthetic methods reported for pholcodine, and the reported synthetic methods are usually to synthesize morpholine into morpholine ethanol, then chlorinate it into ethyl morpholine hydrochloride, and finally form it by condensat...

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): C07D489/02
CPCC07B2200/07C07D489/02
Inventor 赵伟刘杨王孟华曾华荣张建勋周雪平熊秀琳于飞赵晓柯
Owner YICHANG HUMANWELL PHARMA
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