Cis-tetrahydrocarboline intermediate, its synthesis method and its application in the preparation of tadalafil
A technology of tetrahydrocarboline and its synthesis method, which is applied in the field of cis-tetrahydrocarboline intermediate and its synthesis, and the preparation of tadalafil, which can solve the problems of inconvenient purchase and use, and achieve loss avoidance, process stability, and wider use efficiency effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0037] Add 25.5 g of D-tryptophan methyl ester hydrochloride to the reaction flask, add 150 ml of isopropanol at room temperature, stir, add 1.2 equivalents of 3,4-dihydroxybenzaldehyde, and react at 85°C for 8 hours until the raw material The reaction was basically completed, cooled to room temperature, filtered, and the solid was washed with 50 ml of isopropanol, and then dried in an oven to constant weight. 34.6 g of compound I were obtained with a yield of 92%. The synthetic route map is attached figure 1 shown.
Embodiment 2
[0039] Add 25.5 g of D-tryptophan methyl ester hydrochloride to the reaction flask, add 250 ml of propionitrile at room temperature, stir, add 1.5 equivalents of 3,4-dihydroxybenzaldehyde, and react at 85°C for 16 hours until the raw materials are basically The reaction was completed, cooled to room temperature, filtered, and the solid was washed with 50 ml of isopropanol, and then dried in an oven to constant weight. 34.2 g of compound I were obtained in a yield of 97%. The synthetic route map is attached figure 1 shown.
Embodiment 3
[0041] Add 25.5 g of D-tryptophan methyl ester hydrochloride to the reaction flask, add 375 ml of methanol at room temperature, stir, add 1.5 equivalents of 3,4-dihydroxybenzaldehyde, and react at 60°C for 24 hours until the raw materials are basically reacted Complete, cooled to room temperature, filtered, and the solid was washed with 50 mL of methanol, then dried in an oven to constant weight. 33.8 g of compound I were obtained in a yield of 90%. The synthetic route map is attached figure 1 shown.
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