5HT2A receptor antagonist and medical application thereof

A technology of solvates and stereoisomers, applied in the field of medicine, can solve problems such as abnormal motor function and type 2 diabetes

Active Publication Date: 2021-08-06
HAN YUAN MEDI PHARM CO LTD
View PDF7 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the second-generation antipsychotic drugs all have broad-spectrum receptor activity, and these compounds act as agonists, competitive antagonists or inverse agonists to regulate various monoaminergic receptors s...

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
  • 5HT2A receptor antagonist and medical application thereof
  • 5HT2A receptor antagonist and medical application thereof
  • 5HT2A receptor antagonist and medical application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0108] Example 1: Synthesis of 3-(chroman-6-ylmethyl)-1-(4-fluoro-benzyl)-1-(1-methyl-piperidin-4-yl)-urea (compound# 45), ER10058

[0109]

[0110] A solution of triphosgene (148 mg, 0.500 mmol) in DCM (5.0 mL) was slowly added to chroman-6-yl-methylamine mono-hydrochloric acid (99 mg, 0.500 mmol) and triethylamine (50 mg, 0.500 mmol) at 0 °C ) in DCM (5.0 mL). The mixture was stirred at room temperature for 1 hour. Ice water (20 mL) was added, and the mixture was extracted with DCM (20 mL×2). The organic phase was washed with brine, washed with Na 2 SO 4 Drying, filtration and concentration under vacuum gave the product (45-1) as an oil (80 mg, 85% yield).

[0111]

[0112] To a solution of 1-methyl-piperidin-4-ylamine (19 g, 88 mmol) in 500.0 mL of dichloromethane at room temperature was added 4-fluorobenzaldehyde (11 g, 90 mmol), followed by the slow addition of triacetoxy Sodium borohydride (33g, 180mmol), and 10ml acetic acid. The mixture was stirred overnig...

Embodiment 2

[0115] Embodiment 2: Synthesis of 3-(chroman-6-ylmethyl)-1-(4-fluorobenzyl)-1-((1-methylazetidin-3-yl) methyl)urea ( H001-064)ER10191

[0116]

[0117] 3-(chroman-6-ylmethyl)-1-(4-fluorobenzyl)-1-((1-methylazetidin-3-yl)methyl)urea (H001-064) ER10191 The synthesis method was similar to compound #45: using chromane-6-methylisocyanate (45-1) (0.25 mmol) gave white solid H001-064 (12 mg, 12% yield). LCMS: [M+1] + 398.3.

Embodiment 3

[0118] Example 3: Synthesis of (S)-3-(chroman-6-ylmethyl)-1-(4-fluorobenzyl)-1-((1-methylpyrrolidin-2-yl)methyl ) urea (H001-065) ER10192

[0119]

[0120] (S)-3-(chroman-6-ylmethyl)-1-(4-fluorobenzyl)-1-((1-methylpyrrolidin-2-yl)methyl)urea (H001- 065)ER10192

[0121]The synthesis method was similar to compound #45: using chromane-6-methylisocyanate (45-1) (0.5 mmol) gave white solid H001-065 (70 mg, 34% yield). LCMS: [M+1] + 412.3.

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 provides a compound with a central nervous system disease treatment effect and a structure shown represented by formula I. The compound has 5-HT2A receptor antagonist or inverse agonist activity, and has the advantages of high selectivity to 5-HT2A receptors, low cardiotoxicity, good metabolic stability, and no toxic or side effect. The compound can be used for treating certain mental diseases (such as depression, anxiety, psychosis, schizophrenia, insomnia and autism) and mental disorder symptoms related to or concurrent with central nervous system degenerative diseases (such as Alzheimer's disease, Parkinson's disease, Huntington's disease and Lewy small body dementia).

Description

technical field [0001] The invention belongs to the technical field of medicine, and relates to a 5-HT2A receptor antagonist or inverse agonist with therapeutic effect on central nervous system diseases and application thereof. Said compound can be used for the treatment of certain mental illnesses (such as depression, anxiety, psychosis, schizophrenia, insomnia, autism, etc.) and degenerative diseases of the central nervous system (such as Alzheimer's disease, Parkinson's disease, Huntington's disease, dementia with Lewy bodies, etc.) related or concurrent mental disorder symptoms. Background technique [0002] Serotonin or 5-hydroxytryptamine (5-HT) plays an extremely important role in the physiological functions of the human body. In the central nervous system, 5-HT is an important neurotransmitter and neuromodulator, which regulates various behaviors such as sleep, diet, activity, learning and memory, body temperature, blood pressure and pathological states (such as anx...

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): C07D405/12A61K31/4025A61K31/453A61K31/397A61P25/18A61P25/28A61P25/24A61P25/22A61P25/20A61P25/00A61P25/16A61P25/14
CPCC07D405/12A61P25/18A61P25/28A61P25/24A61P25/22A61P25/20A61P25/00A61P25/16A61P25/14A61K31/397A61K31/4025A61K31/453
Inventor 邢洪涛
Owner HAN YUAN MEDI PHARM CO LTD
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