Resolution method of levocetirizine chiral intermediates
A chiral intermediate, levocetirizine technology, applied in organic chemistry methods, chemical instruments and methods, separation of optically active compounds, etc., to achieve convenient post-processing, less waste, and high efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0024] Add 287 g (1 mole) of 1-[(4-chlorophenyl)benzyl]piperazine and 3 moles of chiral tartrate ionic liquid into the reaction vessel, react at 50°C for 5 hours, and extract with 200 ml of toluene , the extracted reaction system was adjusted to pH=11-12 with 10% sodium hydroxide solution, then extracted three times with 200 ml of toluene, combined the toluene solution, dried over anhydrous sodium sulfate, filtered, concentrated, n-hexane crystallized to obtain white Crystalline powder product 52g, yield 36%, melting point: 94-96°C, specific rotation: [α] D ≤-21.5° (C1, toluene), optical purity: ≥99.0%, content: ≥99.0%.
Embodiment 2
[0026] Add 287 g (1 mole) of 1-[(4-chlorophenyl)benzyl]piperazine and 1 mole of chiral lactic acid ionic liquid into the reaction vessel, react at 10°C for 10 hours, and extract with 200 ml of toluene , the reaction system after extraction is adjusted to pH = 11-12 with 10% sodium hydroxide in mass percentage concentration, and then extracted three times with 200 ml of toluene, combined toluene solution, dried over anhydrous sodium sulfate, filtered, concentrated, n-hexane Alkanes were crystallized to obtain 49 grams of white crystalline powder product, yield 34%, melting point: 94-96°C, specific rotation: [α] D ≤-21.5° (C1, toluene), optical purity: ≥99.0%, content: ≥99.0%.
Embodiment 3
[0028] Add 287 g (1 mole) of 1-[(4-chlorophenyl)benzyl]piperazine and 2 moles of chiral mandelic acid ionic liquid into the reaction vessel, react at 60°C for 10 hours, and use 200 ml of toluene Extraction, the extracted reaction system is adjusted to pH = 11-12 with 10% sodium hydroxide solution by mass percentage, then extracted three times with 200 ml of toluene, combined toluene solution, dried over anhydrous sodium sulfate, filtered and concentrated , crystallized from n-hexane to obtain 53 grams of white crystalline powder product, yield 37%, melting point: 94-96°C, specific rotation: [α] D ≤-21.5° (C1, toluene), optical purity: ≥99.0%, content: ≥99.0%.
PUM
Property | Measurement | Unit |
---|---|---|
melting point | aaaaa | aaaaa |
specific rotation | aaaaa | aaaaa |
optical purity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
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