Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!
A cannabinoid receptor 2 (cb2) agonist
What is Al technical title?
Al technical title is built by PatSnap Al team. It summarizes the technical point description of the patent document.
A compound, medicinal salt technology, applied in the field of cannabinoid receptor 2 (CB2) agonists
Active Publication Date: 2018-10-12
CHENGDU UNIVERSITY OF TECHNOLOGY
View PDF3 Cites 0 Cited by
Summary
Abstract
Description
Claims
Application Information
AI Technical Summary
This helps you quickly interpret patents by identifying the three key elements:
Problems solved by technology
Method used
Benefits of technology
Problems solved by technology
[0005] The diverse clinical application value of CB2 receptor agonists shows its broad prospects in the field of medicine. However, so far, no CB2 receptor agonists have become marketed drugs. Better druggable CB2 receptor agonists are of great significance to this field
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
Click on the blue label to locate the original text in one second.
Reading with bidirectional positioning of images and text.
Smart Image
Examples
Experimental program
Comparison scheme
Effect test
Embodiment
[0022] The first step: the preparation of 4-[2-(trifluoromethoxy)phenyl]piperidine-1-carbonitrile
[0023]
[0024] Add 4-[2-(trifluoromethoxy)phenyl]piperidine (10.0g, 40.8mmol), potassium carbonate (11.1g, 80.2mmol) to 100mL dichloromethane / water (1:1), Stir and cool to 0°C. Slowly drop cyanobromide (5.3 g, 50.0 mmol) dissolved in 20 mL of dichloromethane into the above solution, react at 0°C for 30 min, return to room temperature and continue the reaction for 2 h, separate the organic layer, and use saturated sodium bicarbonate solution to saturate The organic layer was washed with sodium chloride solution, dried over anhydrous magnesium sulfate, and the organic phase was concentrated under reduced pressure. The crude product was subjected to silica gel column chromatography (petroleum ether / ethyl acetate=7 / 3) to obtain 4-[2-(trifluoromethoxy 8.9 g of phenyl]piperidine-1-carbonitrile (yield: 81%).
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
Login to View More
Abstract
The invention relates to a propanamide coupled piperidinoxadiazole and imidazo[1,2-a]pyrazine derivative shown as a formula I and / or medicinal salts thereof and a preparation method thereof, as well as a pharmaceutical composition comprising the compound. The compound shown as the formula I is a potential cannabinoid receptor 2(CB2) agonist and can be used for treating and / or preventing diseases such as inflammation, inflammatory bowel diseases, glaucoma, diabetes, nephropathy, cardiomyopathy and the like. The structural formula is as shown in the specification, wherein R1 is aryl and heteroaryl; and R2 is H, (C1-C6) linear alkyl or branched alkyl.
Description
technical field [0001] The invention belongs to the field of medicinal chemistry, and specifically relates to a propionamide-linked piperidinyl oxadiazole and imidazo[1,2-a]pyrazine compounds and physiologically acceptable salts thereof described in the claims , their preparation methods and their role in the prevention and / or treatment of pain, inflammation, inflammatory bowel disease, glaucoma, diabetes, diabetic retinopathy, atherosclerosis, age-related macular degeneration, acute liver failure, liver fibrosis, Pulmonary fibrosis, renal fibrosis, systemic fibrosis, ischemia-reperfusion injury, acute allograft rejection, chronic allograft nephropathy, diabetic nephropathy, glomerular nephropathy, cardiomyopathy, heart failure, myocardial ischemia Blood, myocardial infarction, systemic sclerosis, thermal injury, burns, hypertrophic scars, gingivitis fever, liver cirrhosis or tumors, osteoporosis, neurodegeneration, stroke and other cannabinoid receptor 2 (CB2) agonist-related...
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
Application Date:The date an application was filed.
Publication Date:The date a patent or application was officially published.
First Publication Date:The earliest publication date of a patent with the same application number.
Issue Date:Publication date of the patent grant document.
PCT Entry Date:The Entry date of PCT National Phase.
Estimated Expiry Date:The statutory expiry date of a patent right according to the Patent Law, and it is the longest term of protection that the patent right can achieve without the termination of the patent right due to other reasons(Term extension factor has been taken into account ).
Invalid Date:Actual expiry date is based on effective date or publication date of legal transaction data of invalid patent.