-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
The Production Process of 3-[[6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy[2-(4-morpholinyl)ethyl]-4H-1-benzopyran-4-one: A Comprehensive Overview
In the world of chemical synthesis, the creation of novel compounds with unique properties is a constant endeavor.
One such compound, 3-[[6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy[2-(4-morpholinyl)ethyl]-4H-1-benzopyran-4-one, is a fascinating example of this pursuit.
This compound, also known as Morpholinium 1-benzopyran-4-yl-α-(D-glucopyranosyl)-6-O-[(6S)-6-(dihydroxyphenyl)-2H-pyran-2-yl]-α-L-mannopyranoside, is a complex organic molecule with multiple functional groups and a unique structural configuration.
In this article, we will take a comprehensive look at the production process of this compound, exploring the various steps involved and the methodologies used to synthesize it.
Step 1: Synthesis of the Alpha-L-Mannopyranosyl Precursor
The synthesis of the alpha-L-mannopyranosyl precursor, 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl, is the first step in the production process of Morpholinium 1-benzopyran-4-yl-α-(D-glucopyranosyl)-6-O-[(6S)-6-(dihydroxyphenyl)-2H-pyran-2-yl]-α-L-mannopyranoside.
This precursor is synthesized through a multi-step process that involves the condensation of L-mannose and D-glucose, followed by oxidation to form the 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl precursor.
Step 2: Condensation Reaction to Form the Benzopyranyl Unit
Once the alpha-L-mannopyranosyl precursor is synthesized, it is subjected to a condensation reaction with 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy[2-(4-morpholinyl)ethyl]amine.
This reaction results in the formation of the Morpholinium 1-benzopyran-4-yl-α-(D-glucopyranosyl)-6-O-[(6S)-6-(dihydroxyphenyl)-2H-pyran-2-yl]-α-L-mannopyranoside precursor, which is a complex molecule with multiple functional groups.
Step 3: Oxidation Reaction to Form the Final Compound
The Morpholinium 1-benzopyran-4-yl-α-(D-glucopyranosyl)-6-O-[(6S)-6-(dihydroxyphenyl)-2H-pyran-2-yl]-α-L-mannopyranoside precursor is then subjected to an oxidation reaction that results in the formation of the final compound.
This reaction involves the oxidation of the 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyran