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

Synthesis method of octahydro-4A,8-epoxy pyrido [4,3-C]azepine-6(5H)-tert-butyl formate

A technology of tert-butyl formate and epoxypyridine is applied in the field of chemical synthesis to achieve the effect of ingenious reaction design, reasonable reaction process design and cost saving of raw materials

Active Publication Date: 2021-08-06
WUXI APPTEC +1
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the synthesis method of octahydro-4A,8-epoxypyrido[4,3-C]azepine-6(5H)-tert-butyl carboxylate is rarely reported in the literature

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
  • Synthesis method of octahydro-4A,8-epoxy pyrido [4,3-C]azepine-6(5H)-tert-butyl formate
  • Synthesis method of octahydro-4A,8-epoxy pyrido [4,3-C]azepine-6(5H)-tert-butyl formate
  • Synthesis method of octahydro-4A,8-epoxy pyrido [4,3-C]azepine-6(5H)-tert-butyl formate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0066]

[0067] The first step: The catalytic amount of tetraced oxide was added to the compound 1 (24.6 g, 86 mmol) and NMO (15 g, 129 mmol) acetone (500 mL) solution, and the mixture was stirred at room temperature for 4 HRs. TLC (ethyl acetate) was monitored, and water (500 mL) was added to the reaction system, extracted with ethyl acetate (500 ml x 3), combined with an organic phase, dried over anhydrous sodium sulfate, filtered, filtrate to obtain Compound 2 (27 g, 84.6 mmol) is used directly for the next step.

[0068] Step 2: Compound 2 (27 g, 84.6 mmol) was dissolved in methanol (450 mL) and water (50 mL) mixed solvent at room temperature, and sodium metatanate (27 g, 127 mmol) was added, and stirred at room temperature for 4 HRs. TLC (ethyl acetate) monitoring has been completed. Water (500 mL) was added, extracted with dichloromethane (500 ml x 3), combined with an organic phase, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to obtain...

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 synthesis method of octahydro-4A,8-epoxy pyrido[4,3-C]azepine-6(5H)-tert-butyl formate. The synthesis method comprises the following steps: 1, reacting a compound 1 with a catalytic amount of osmium tetroxide and a first oxidant to obtain a compound 2; 2, oxidizing an alcoholic hydroxyl group into an aldehyde group by the compound 2 under the action of a second oxidant to obtain a compound 3; 3, subjecting the compound 3 and benzyl amine to reduction ammoniation in an inert atmosphere under the action of a first reducing agent to obtain a compound 4; 4, subjecting the compound 4 to catalytic hydrogenation through a palladium catalyst in the presence of Boc2O to obtain a compound 5; 5, reducing the compound 5 through a second reducing agent to obtain a compound 6; and 6, carrying out catalytic hydrogenation on the compound 6 under the action of a palladium catalyst to obtain a compound 7. The method disclosed by the invention has the advantages of easily available raw materials, convenience in operation, safety in reaction, suitability for amplification, short route, high total yield, suitability for industrial production and the like.

Description

Technical field [0001] The present invention relates to the field of chemical synthesis, and more particularly to a synthesis method of octal hydrogen-4a, 8-epoxypyridine and [4,3-C] nitrogen-6 (5H)-formic acid tert-butyl ester. Background technique [0002] Compound octahydro-4a, 8-epoxypyridine and [4,3-C] Nazo-6 (5H) -Camhalic acid tert-butyl ester (CAS: 1251010-89-5) and related derivatives in pharmaceutical chemistry And extensive use in organic synthesis. Currently, octahydro-4a, 8-epoxypyridine and [4,3-C] Nazo - 6 (5H) - Synthesis of tert-butyl formate is reported. [0003] Therefore, it is necessary to develop a raw material easy, easy to operate, easy to control, overall yield, suitable for industrial production. Inventive content [0004] The technical problem to be solved by the present invention is to provide a method of synthesizing octahydro-4a, 8-cycloptidine and [4,3-C] azagazo-6 (5H) -tutyl ester, which has The raw materials are easy, easy to operate, safe, eas...

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(China)
IPC IPC(8): C07D498/18
CPCC07D498/18
Inventor 周强张大为孙春于凌波徐学芹毛延军董径超马汝建徐艳白有银兰倩倩高明飞姚宝元赵廷巴苏伟刘双燕
Owner WUXI APPTEC
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