Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Preparation method of tert-butyl-1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate

A diazaspiro, tert-butyl technology, applied in the field of tert-butyl-1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate production , can solve the problem of no suitable industrial synthesis method, etc., and achieve the effect of reasonable reaction process design, easy reaction and short route

Active Publication Date: 2022-05-17
WUXI APPTEC
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Mainly solve the technical problem that there is no suitable industrial synthesis method at present

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
  • Preparation method of tert-butyl-1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0012] Step 1: Compound 1 was dissolved in dichloromethane (1.2 L), and Boc anhydride (480 g, 2.2 mol) dissolved in dichloromethane (600 mL) was added at 20°C. The reaction was then stirred at room temperature 25°C for 12 hours. TLC showed that the reaction of the raw materials was complete, and the reaction solution was washed successively with saturated aqueous sodium bicarbonate (600 mL) and saturated brine (600 mL), and then dried over anhydrous sodium sulfate. The organic phase was dried under vacuum to obtain compound 2 (340 g) as a colorless oil.

[0013] Step 2: Dissolve 3-chloro-2-chloromethyl-1-propene (11.7 g, 0.073 mol) in N,N-dimethylformamide (120 mL), cool to -20°C and add sodium hydrogen (3.7 g, 0.154 mol). After 30 minutes, compound 2 dissolved in N,N-dimethylformamide (20 mL) was added to the reaction system. Then return to room temperature 25°C and stir for 12 hours. The reaction solution was diluted with water (1.4 L) and extracted with methyl tert-buty...

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 relates to a method for preparing tert-butyl-1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate, which mainly solves the problem that there is currently no technology suitable for industrial synthesis methods question. The present invention is divided into six steps: the first step, first dissolving compound 1 in dichloromethane, then adding Boc anhydride, and reacting to obtain compound 2; the second step, compound 2 and sodium hydrogen, 3-chloro-2-chloromethyl ‑1‑propylene reaction to obtain compound 3; in the third step, compound 3 is dissolved in dichloromethane, and m-chloroperoxybenzoic acid is added to react to obtain compound 4; in the fourth step, compound 4 is reacted in 2‑benzylaminoethanol Compound 5 was obtained; in the fifth step, compound 5 was reacted with sodium hydrogen and p-toluenesulfonimidazole in tetrahydrofuran to obtain compound 6; in the sixth step, compound 6 was reacted with palladium hydroxide in methanol to obtain final compound 7.

Description

technical field [0001] The invention relates to a synthesis method of compound tert-butyl-1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate. Background technique [0002] The compound tert-butyl-1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate (CAS: 1251010-99-7) and related derivatives in Medicinal Chemistry It has wide applications in organic synthesis. At present, there are few reports on the synthesis of tert-butyl 1,8-dioxa-4,11-diazaspiro[5.6]dodecane-11-carboxylate. Therefore, it is necessary to develop a synthetic method that is easy to obtain raw materials, easy to operate, easy to control the reaction, suitable for overall yield, and suitable for industrial production. Contents of the invention [0003] The purpose of the present invention is to develop a tert-butyl 1,8-dioxa-4,11-diazaspiro[5.6]dodecane with easy to obtain raw materials, convenient operation, easy to control reaction and high yield Synthesis of alkane-11-carboxylates. It mainly solv...

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): C07D498/10
CPCC07D498/10Y02P20/55
Inventor 张大为周强高明飞姚宝元兰倩倩赵廷王曦卫维魏昕睿谭汝鹏贾涛白有银孙春付新雨于凌波马汝建
Owner WUXI APPTEC
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
Eureka Blog
Learn More
PatSnap group products