Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Synthetic method of Oxazolam drug intermediate 2-amino-5-chlorobenzophenone

A technology of oxazolam and chlorobenzophenone, which is applied in the field of synthesis of 2-amino-5-chlorobenzophenone, an intermediate of oxazolam medicine, can solve the problem of inability to recall, loss and transient anterograde in patients Memory and other problems, to achieve the effect of reducing reaction temperature and reaction time, reducing intermediate links, and improving reaction yield

Inactive Publication Date: 2016-04-06
CHENGDU KA DI FU TECH
View PDF0 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Transient anterograde amnesia following intramuscular or intravenous administration, which prevents the patient from recalling events that occurred during the peak of the drug

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
  • Synthetic method of Oxazolam drug intermediate 2-amino-5-chlorobenzophenone

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0013] In a reaction vessel equipped with a stirrer, a thermometer and a reflux condenser, add 3.51 mol of benzamide (2), raise the temperature of the solution to 120°C, add 1.41 mol of p-chloroaniline (3) dropwise, and slowly heat up after the addition To 190°C, add 5.5mol of stannous chloride, increase the solution temperature to 240-250°C, react at this temperature for 3h, until no gas is generated, lower the solution temperature to 90°C, add 10% chloride by mass Potassium solution 500ml, raise the solution temperature to 130°C and reflux, after 3h, pour out the water layer, after cooling the solution, a dark suspension is precipitated, this suspension is added to 2.5L of 50% phosphoric acid solution by mass fraction, reflux for 20h, After cooling, pour the solution into 1200ml of 20% sodium nitrate solution by mass fraction, reduce the temperature of the solution to 5°C, add 80% cyclohexane for extraction, and add 300ml of 30% sodium sulfite solution to the cyclohexane laye...

example 2

[0015] In a reaction vessel equipped with a stirrer, a thermometer, and a reflux condenser, add 3.53 mol of benzamide (2), raise the temperature of the solution to 121°C, add 1.41 mol of p-chloroaniline (3) dropwise, and slowly raise the temperature after the addition To 192°C, add 5.7 mol of stannous chloride, increase the solution temperature to 246°C, react at this temperature for 3 hours, until no gas is generated, lower the solution temperature to 92°C, and add a 12% potassium chloride solution 500ml, raise the temperature of the solution to reflux at 130°C, after 3h, pour out the water layer, after cooling the solution, a dark suspended substance precipitates, add the suspended substance to 2.5L of 52% phosphoric acid solution, reflux for 21h, after cooling , Pour the solution into 1200ml mass fraction of 22% sodium nitrate solution, reduce the solution temperature to 6°C, add mass fraction of 82% cyclohexane for extraction, add mass fraction of 32% sodium sulfite solutio...

example 3

[0017] In a reaction vessel equipped with a stirrer, a thermometer, and a reflux condenser, add 3.55 mol of benzamide (2), raise the temperature of the solution to 123°C, add 1.41 mol of p-chloroaniline (3) dropwise, and slowly heat up after the addition To 195°C, add 5.9 mol of stannous chloride, raise the solution temperature to 250°C, react at this temperature for 4h, until no gas is generated, lower the solution temperature to 95°C, add a mass fraction of 15% potassium chloride solution 500ml, raise the temperature of the solution to reflux at 130°C, after 4 hours, pour out the water layer, after cooling the solution, a dark suspended substance precipitates, add the suspended substance to 2.5L of 55% phosphoric acid solution, reflux for 23h, after cooling , Pour the solution into 1200ml mass fraction of 25% sodium nitrate solution, reduce the temperature of the solution to 8°C, add mass fraction of 85% cyclohexane for extraction, add mass fraction of 35% sodium sulfite solu...

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

A synthetic method of an Oxazolam drug intermediate 2-amino-5-chlorobenzophenone comprises the following steps: adding 3.51-3.55mol of benzamide into a reaction container provided with a stirrer, a thermometer and a reflux condenser, rising the temperature of a solution to 120-123 DEG C, dropwise adding 1.41mol of p-chloroaniline, after adding, slowly rising the temperature to 190-195 DEG C, adding 5.5-5.9 mol of stannous chloride, rising the temperature of a solution to 240-250 DEG C, reacting for 3-4h at the temperature until no gas is generated, reducing the temperature of a solution to 90-95 DEG C, adding 500ml of a potassium chloride solution, rising the temperature of a solution to 130 DEG C, performing backflow, pouring out a water layer after 3-4h, cooling a solution, then separating out a dark suspended matter, adding the suspended matter into 2.5L of a phosphoric acid solution, performing backflow for 20-23h, cooling, then pouring a solution into 1200ml of a sodium nitrate solution, reducing the temperature of a solution to 5-8 DEG C, adding cyclohexane for extraction, adding 300ml of a sodium sulfite solution in a cyclohexane layer, performing reduced pressure distillation, adding acetonitrile and extracting for 5-7 times, separating out a solid, filtering, and dehydrating by a dehydrating agent, thus obtaining the yellow crystal 2-amino-5-chlorobenzophenone.

Description

technical field [0001] The invention relates to a method for synthesizing oxazolam drug intermediate 2-amino-5-chlorobenzophenone. Background technique [0002] Oxazolam drugs produce anxiolytic, sedative, hypnotic, anticonvulsant, and muscle relaxant effects. After intramuscular or intravenous administration, transient anterograde amnesia can occur, making patients unable to recall events that occurred during the peak period of the drug. This product is characterized by its rapid onset and short duration of action. After taking the medicine, the time to fall asleep can be shortened (generally it only takes 20 minutes from taking the medicine to falling asleep), and the total sleep time can be prolonged without affecting the rapid wave sleep (REM). After waking up in the next morning, the patient can feel energetic, relaxed and happy. No tolerance and withdrawal symptoms or rebound. Low toxicity and large safety range. Both oral administration and intramuscular injection...

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
IPC IPC(8): C07C221/00C07C225/22
CPCC07C221/00
Inventor 廖如佴
Owner CHENGDU KA DI FU 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
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