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

Process for producing racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo [4.3.0] nonyl hydride

A kind of diazabicyclo, dioxo technology, applied in the field of preparation of fine chemical products

Inactive Publication Date: 2010-12-15
EAST CHINA NORMAL UNIV
View PDF2 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It is then reduced to racemic cis 8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane by high-pressure hydrogenation, thereby overcoming the prior art Existing defects such as intense reaction conditions and complicated operation

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
  • Process for producing racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo [4.3.0] nonyl hydride
  • Process for producing racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo [4.3.0] nonyl hydride
  • Process for producing racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo [4.3.0] nonyl hydride

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] The first step, dehydrogenation of (1R, 6S)-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane: add 5g to 1000ml single-necked bottle (1R,6S)-8-Benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane (e.e. value 83%), 25g manganese dioxide, 120g tetrahydrofuran, oil The bath was heated to 60°C for 10 hours. Cool down to room temperature, recover manganese dioxide (filter residue) by suction filtration, and remove the solvent from the filtrate: add 100ml of dichloromethane to dissolve, wash with a small amount of 5% dilute hydrochloric acid, dry over anhydrous sodium sulfate, and remove the solvent to obtain 4.6g of dark yellow solid. The yield of 6-benzyl-5,7-dioxo-1,2,3,4-tetrahydro-pyrrolo[3,4-b]pyridine was 93%. Mp.: 106~108℃; 1 HNMR (CDCl 3 ): δppm: 1.86 (2H, m), 2.34 (2H, t, J=6Hz), 3.36 (2H, t, J=5Hz), 4.60 (2H, s), 7.26~7.35 (5H, m).

[0031] The second step, high-pressure hydrogenation of 6-benzyl-5,7-dioxo-1,2,3,4-tetrahydro-pyrrolo[3,4-b]pyridine: 60g6-benzyl-5 , 7-...

Embodiment 2

[0033] The first step, dehydrogenation of (1R,6S)-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane:

[0034] Add 0.5g (1R, 6S)-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane (e.e. value 98%) in 100ml single-necked bottle, 2.5g of manganese dioxide and 10g of toluene were heated in an oil bath to reflux at 110°C for 7 hours. Cool down to room temperature, recover manganese dioxide by suction filtration, and remove the solvent from the filtrate: add 10ml of dichloromethane to dissolve, wash with a small amount of 5% dilute hydrochloric acid, dry over anhydrous sodium sulfate, and remove the solvent to obtain 0.45g of 6-benzyl as a dark yellow solid Base-5,7dioxo-1,2,3,4-tetrahydro-pyrrolo[3,4-b]pyridine, the yield was 91%. The melting point and NMR data are the same as those of 6-benzyl-5,7-dioxo-1,2,3,4 tetrahydro-pyrrolo[3,4-b]pyridine in Example 1.

[0035] The second step, high-pressure hydrogenation of 6-benzyl-5,7-dioxo-1,2,3,4-tetrahydro-pyrrolo[3,4-b]pyridine: 20g6-ben...

Embodiment 3

[0037] The first step, dehydrogenation of (1R,6S)8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane:

[0038] Add 0.5g (1R, 6S)-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane (e.e. value 90%) in 100ml single-necked bottle, 2.5 g manganese dioxide, 2 g cyclohexane, heated to 80°C in an oil bath and refluxed for 5 hours. Cool down to room temperature, recover manganese dioxide by suction filtration, remove the solvent from the filtrate, add 10ml of dichloromethane to dissolve, wash with a small amount of 5% dilute hydrochloric acid, dry over anhydrous sodium sulfate, and remove the solvent to obtain 0.47g of 6-benzyl as a dark yellow solid Base-5,7dioxo-1,2,3,4-tetrahydro-pyrrolo[3,4-b]pyridine, the yield was 95%. The melting point and NMR data are the same as those of 6-benzyl-5,7dioxo-1,2,3,4-tetrahydro-pyrrolo[3,4-b]pyridine in Example 1.

[0039] The second step, the high-pressure hydrogenation of 6-benzyl-5,7-dioxo-1,2,3,4 tetrahydro-pyrrolo[3,4-b]pyridine: 2096-benzyl-5,...

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 method for preparing racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo[4.3.0]nonane, which relates to a racemization method for (1R,6S)-cis-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane. Firstly, the (1R,6S)-cis-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane is refluxed for 3 to 10h in the presence of a manganese dioxide catalyst and a dehydrogenation solvent at a temperature of between 60 and 110 DEG C for an oxydehydrogenation reaction, and then obtained 6-benzyl-5,7-dioxo-1,2,3,4-tetrahydro-pyrido[3,4-b]pyridine reacts for 5 to 10 h in the presence of a Pd / C or PtO2 catalyst and a hydrogenation solvent at a temperature of between 70 and 100 DEG C at the pressure of between 5 and 9MPa and is reduced into the racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo[4.3.0]nonane. The method has the advantages of simple process, quick reaction, more than 90 percent of two-step overall yield, mild conditions, simple treatment after the reaction, no secondary reactions, and reutilized catalyst, and meets the requirement of environmental protection. The obtained product is the racemic cis-8-benzyl-7, 9-dioxo-2, 8-diazabicyclo[4.3.0]nonane, fully avoids the generation of trans-products, can be directly used for optical resolution, and remarkably improves the utilization rate of raw materials.

Description

technical field [0001] A process for the preparation of racemic cis 8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane involving a (1R,6S)-cis 8- The invention relates to a racemization method of benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane, which belongs to the technical field of preparation of fine chemical products such as medicine. Background technique [0002] Chiral cis 8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane is a synthetic antibacterial drug such as the fourth generation of new extended-spectrum fluoroquinolone antibacterial drugs- Moxifloxacin (EP-550903), antifungal drugs (JP-2005-97298) and food additives are key intermediates of fine chemicals, which are more and more widely used in industry. At present, it is most widely used in the synthesis of (S, S)-2,8-diazabicyclo[4.3.0]nonane. [0003] [0004] It can be seen from the above formula that only (1S,6R)-cis 8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane is actually used. And its enantiomer (1R,...

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): C07D471/04B01J23/34
CPCY02P20/584
Inventor 邹新琢蔡惠华郑祖彪
Owner EAST CHINA NORMAL UNIV
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