Tapentadol carbamate derivative and preparation method and application thereof

A carbamate, tapentadol technology, applied in the preparation of carbamate derivatives, the preparation of organic compounds, the active ingredients of esters, etc. Stability, effect on improving oral bioavailability

Inactive Publication Date: 2010-09-29
SHENYANG PHARMA UNIVERSITY +1
View PDF8 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This kind of carrier fragment enters the body and is difficult to metabolize and release the prodrug, a

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
  • Tapentadol carbamate derivative and preparation method and application thereof
  • Tapentadol carbamate derivative and preparation method and application thereof
  • Tapentadol carbamate derivative and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

Embodiment 2

Embodiment 3

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 belongs to the field of pharmacy, in particular to a tapentadol carbamate derivative with a general formula I, pharmaceutically acceptable salts, a preparation method and an application thereof. In the invention, the structure of phenolic hydroxyl groups in tapentadol molecules is improved by a chemical synthesis method, and proper carrier groups are introduced in the position to synthesize carbamate type prodrug. All amines adopted by the carbamate are fatty amines, wherein dimethylamine or methylamine fragments can generate demethylation metabolism easily in vivo, thereby being convenient for releasing raw tapentadol. Meanwhile, the existence of the carbamate structure increases the chemical stability of the prodrug and can obviously improve the oral bioavailability, reduce the administration dosage and lower the toxic side effect, and the tapentadol carbamate derivative can be further developed into novel tapentadol analgesics.

Description

technical field The invention belongs to the field of pharmacy and relates to carbamate derivatives of tapentadol and its preparation and application. Background technique Tapentadol HCl is a new type of centrally acting analgesic drug developed by Johnson & Johnson Company of the United States with a dual mechanism of action. It is used as a single isomer of (1R, 2R), molecular formula C 14 h 24 ClNO, chemical name (1R, 2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol Hydrochloride. Tapentadol belongs to 1-phenyl-3-dimethylaminopropane compounds, which have various pharmacological activities and can be used to relieve pain (EP693475), and can also be used to treat psychosis (DE102007012165), depression (DE10233048 ), urinary incontinence (WO2002043715), etc. Tapentadol was approved for marketing by the U.S. Food and Drug Administration (FDA) on November 21, 2008. It has been clinically shown that it has good efficacy between morphine and tramadol, and can achieve...

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): C07C271/44C07C271/48C07C271/00C07D295/205C07D211/16C07C269/00A61K31/27A61K31/4453A61K31/40A61K31/445A61K31/5375A61P29/00
Inventor 许佑君王文娟傅鼎鼎常燕南何仲贵
Owner SHENYANG PHARMA UNIVERSITY
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
Try Eureka
PatSnap group products