Mixed inhibitors of aminopeptidase n and of neprilysine
A compound and cyclic compound technology, applied in the field of mixed inhibitors of aminopeptidase N and enkephalinase
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0245] The invention is further elucidated below, but it is not limited in any way to the following examples.
[0246] 1. Synthesis of NEP–APN Mixed Inhibitors
[0247] 1.1 Synthesis of NEP inhibitors
[0248] 1.1.1 step 1 : Synthesis of (R)–2–Bromocarboxylic Acid
[0249]
[0250] The (R)-configuration amino acid (39.3 mmol) was dissolved in 50 mL of water. At 0°C, KBr (3.5eq, 31.8g) and then H 2 SO 4 (7.73 mL), while maintaining the temperature below 5°C. The mixture was cooled to -10 °C and NaNO dissolved in 17 mL of water was added dropwise 2 (1.3eq, 3.59g). The mixture was stirred at -5°C for 2 hours.
[0251] After returning to room temperature, CH 2 Cl 2 (2 x 50 mL) to extract the mixture. with H 2 O, saturated NaCl washing organic phase, NaCl 2 SO 4 Drying afforded the expected (R) configuration product.
[0252] 3a R 2 =CH 2 Ph: pale yellow oil; (yield: 50%); Rf(CH 2 Cl 2 / MeOH):0.62
[0253] NMR (abbreviated as RMN in French) (CDCl 3 ,200MH...
PUM
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