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

The preparation method of 2-trifluoromethyl-1-benzyloxycarbonyl-1-azacycloalkane

A technology of azacycloalkane and benzyloxycarbonyl, which is applied in the field of preparation of 2-trifluoromethyl-1-benzyloxycarbonyl-1-azacycloalkane, can solve the problem that the α-substituted azacycloalkane has long steps, Low yield, unsuitable for amplification, etc., to achieve the effects of low yield, improved yield, and improved drug-like properties

Active Publication Date: 2018-01-12
武汉药明康德新药开发有限公司
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The method prepares α-substituted azacycloalkane with long steps and low yield, especially for azepane yield as low as 10%
Therefore, this method is not suitable for the amplification of the reaction and has considerable limitations.

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
  • The preparation method of 2-trifluoromethyl-1-benzyloxycarbonyl-1-azacycloalkane
  • The preparation method of 2-trifluoromethyl-1-benzyloxycarbonyl-1-azacycloalkane
  • The preparation method of 2-trifluoromethyl-1-benzyloxycarbonyl-1-azacycloalkane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Example 1: Preparation of 2-oxa-benzyloxycarbonyl cycloheptylamine 2c

[0019]

[0020] Steps:

[0021] Under nitrogen protection, compound cycloheptamide 1c (20 grams, 0.23 moles) and tetrahydrofuran (200 milliliters) were added in a dry three-necked flask, and n-butyllithium (94 milliliters, 0.23 moles, 2.5 M n-hexane solution). The reaction solution was stirred at -78°C for 60 minutes, and then a solution of benzyl chloroformate (40 g, 0.23 mol) in THF (50 mL) was slowly added. Slowly rise to room temperature and stir for 10 hours, quench with saturated ammonium chloride aqueous solution, extract with ethyl acetate, dry and concentrate the organic phase to obtain 53 g of product 2-oxa-benzyloxycarbonylcycloheptylamine 2c, yield 100%. used directly in the next reaction.

Embodiment 2

[0022] Example 2: Preparation of 2-oxa-1-benzyloxycarbonylpyrroline 2a

[0023] When n=1, the operation is the same as in Example 1. The yield is 100%. used directly in the next reaction.

Embodiment 3

[0024] Example 3: Preparation of 2-oxa-1-benzyloxycarbonylpiperidine 2b

[0025] When n=2, the operation is the same as in Example 1. The yield is 70%. used directly in the next reaction.

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 discloses a preparation method of 2-trifluoromethyl-1-carbobenzoxy-1-aza-cyclane, and mainly solves the problems that the step of the preparation of alpha-position trifluoromethyl aza-cyclane is long, the yield is low, and the like. The method comprises the steps that aza-cyclane-2-ketone is taken as starting material; the starting material is conducted to Cbz protection, so as to obtain 2-oxa-1-carbobenzoxy-1-aza-cyclane; the 2-oxa-1-carbobenzoxy-1-aza-cyclane is reacted with trifluoromethylation reagent, so as to obtain 2-hydroxy-2-trifluoromethyl-1-carbobenzoxy-1-aza-cyclane; and the compound is conducted to hydrogenation deprotection, so as to obtain the 2-trifluoromethyl-1-carbobenzoxy-1-aza-cyclane. The overall yield is 13 to 35.8 percent.

Description

technical field [0001] The invention relates to a preparation method of 2-trifluoromethyl-1-benzyloxycarbonyl-1-azacycloalkane. Background technique [0002] Nitrogen-α-substituted azacycloalkanes are an important class of nitrogen-containing heterocyclic rings. Except some exist in natural products, they are also useful groups for constructing a wide variety of biological activities. This type of heterocycle has the characteristics of many alkaloids, and many literatures have reported that compounds containing this type of heterocycle have been studied clinically or preclinically. This type of compound is a class of molecules with a relatively special structure, which can effectively link and integrate key pharmacophore units into its rigid structure to form molecules with special spatial configurations / conformations, which can match the different biomacromolecules in the organism. Spatial structure, resulting in different biological activities or utility. So far, there a...

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 Patents(China)
IPC IPC(8): C07D207/08C07D211/18C07D223/04
Inventor 公衍之刘德军段建军董径超吴颢马汝建陈曙辉林寿忠
Owner 武汉药明康德新药开发有限公司
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