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

3,4-dihydrobenzoxazine compounds and inhibitors of vanilloid receptor subtype 1 (VRI) activity

a vanilloid receptor and inhibitory technology, applied in the field of new drugs, to achieve the effect of effective inhibition of vanilloid receptors, excellent inhibitory effect on vr1 activity, and effective medical treatment and/or prevention

Inactive Publication Date: 2011-09-01
JAPAN TOBACCO INC
View PDF58 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

As well as capsaicin, heat and acid also cause pain and it is known that the capsaicin sensitive nociceptive nerves respond to two or more types of stimulation.

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
  • 3,4-dihydrobenzoxazine compounds and inhibitors of vanilloid receptor subtype 1 (VRI) activity
  • 3,4-dihydrobenzoxazine compounds and inhibitors of vanilloid receptor subtype 1 (VRI) activity
  • 3,4-dihydrobenzoxazine compounds and inhibitors of vanilloid receptor subtype 1 (VRI) activity

Examples

Experimental program
Comparison scheme
Effect test

example 1-1

Production of (S)-4-(5-picoline-2-yl)-3-hydroxymethyl-N-(4-tert-butoxy-3,5-difluorophenyl)-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxamide

First Step

Production of methyl 3-nitrosalicylate

[0185]3-Nitrosalicylic acid (500 g) was dissolved in methanol (2.25 L), concentrated sulfuric acid (0.25 L) was added, and the mixture was refluxed for 22 hours. The reaction solution was cooled on ice, and the precipitated solid was collected by filtration and dried to obtain the title compound (517.3 g).

[0186](400 MHz, DMSO-d6): 3.95 (s, 3H), 7.16 (t, J=8.1 Hz, 1H), 8.11 (dd, J=7.9, 1.9 Hz, 1H), 8.21 (dd, J=8.3, 1.9 Hz, 1H), 11.49 (s, 1H).

Second Step

Production of methyl 2-(2-methoxyethoxy)methyloxy-3-nitrobenzoate

[0187]Methyl 3-nitrosalicylate (516.3 g) obtained in the preceding step was dissolved in N,N-dimethylformamide (2.0 L), potassium carbonate (362 g) was added, 1-chloromethoxy-2-methoxyethane (0.329 L) was further added with stirring under ice-cooling, and the mixture was stirred at room tem...

example 1-2

Production of (S)-4-(5-picoline-2-yl)-3-hydroxymethyl-N-(3,5-difluoro-4-isopropoxyphenyl)-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxamide

[0199](S)-4-(5-picoline-2-yl)-3-hydroxymethyl-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (400 mg) obtained in the Seventh Step of Example 1-1 was dissolved in N,N-dimethylformamide (2 mL). 3,5-Difluoro-4-isopropoxyaniline (249 mg), 1-hydroxybenzotriazole (204 mg) and 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (281 mg) were added in this order and the mixture was stirred overnight at room temperature. Water and a saturated sodium hydrogencarbonate solution were added to the reaction solution and then extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by silica gel chromatography (hexane:ethyl acetate=4:3) to obtain the title compound (332 mg).

example 1-3

Production of (S)-4-(5-picoline-2-yl)-3-hydroxymethyl-N-(3,5-difluoro-4-ethoxyphenyl)-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxamide

[0200](S)-4-(5-picoline-2-yl)-3-hydroxymethyl-3,4-dihydro-2H-benzo[1,4]oxazine-8-carboxylic acid (400 mg) obtained in the Seventh Step of Example 1-1 was dissolved in N,N-dimethylformamide (2 mL). 3,5-Difluoro-4-ethoxyaniline (230 mg), 1-hydroxybenzotriazole (204 mg) and 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (281 mg) were added in this order and the mixture was stirred overnight at room temperature. Water and a saturated sodium hydrogencarbonate solution were added to the reaction solution and then extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by silica gel chromatography (hexane:ethyl acetate=5:4) to obtain the title compound (358 mg).

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 3,4-dihydrobenzoxazine compound of the present invention is represented by the following formula [1] (wherein X is a nitrogen atom or CR3; R1 is a hydrogen atom or a halogen atom; R2 is a C1-6 alkoxy group which may be substituted with the same or different 1 to 5 substituents selected from a halogen atom and a hydroxyl group; and R3 is a halogen atom. However, R1 is a halogen atom when X is CR3). This compound is effective in treating diseases to which the vanilloid receptor subtype 1 (VR1) activity is involved, such as pain, etc.

Description

TECHNICAL FIELD[0001]The present invention relates to a novel 3,4-dihydrobenzoxazine compound having an inhibitory effect on vanilloid receptor subtype 1 (VR1) activity and a pharmaceutically acceptable salt thereof, a pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient, and a method for treating and / or preventing diseases to which the vanilloid receptor subtype 1 (VR1) activity is involved, such as pain, acute pain, chronic pain, neuropathic pain, rheumatoid arthritis pain, neuralgia, etc., particularly pain.BACKGROUND ART[0002]Capsaicin, which is the main ingredient of red pepper, is a pungency causing ingredient as well as a pain producing substance. It has been reported that many nociceptive nerves, particularly unmyelinated C fibers have capsaicin sensitivity and it is known that C fibers will selectively drop out when capsaicin is administered to an infant rodent. It has been also reported that there are many s...

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 Applications(United States)
IPC IPC(8): A61K31/538C07D413/04C07D413/14A61P25/24A61P25/04A61P31/12A61P29/00A61P17/00A61P11/06A61P1/04A61P13/00
CPCC07D413/14C07D413/04A61P1/04A61P11/06A61P13/00A61P17/00A61P25/04A61P25/24A61P29/00A61P31/12
Inventor KOGA, YOSHIHISAYATA, SHINJIYAMASAKI, TAKAYUKIMATSUMOTO, TATSUYASAKATA, MASAHIROKONDO, WATARUHORI, YOSHIKAZU
Owner JAPAN TOBACCO INC
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