-
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
Barnidipine hydrochloride is a pharmaceutical drug that is commonly used to treat hypertension and other cardiovascular conditions.
It belongs to a class of drugs known as dihydropyridine calcium channel blockers, which work by relaxing the smooth muscle in the walls of blood vessels, causing them to widen and allowing blood to flow more easily.
In this article, we will discuss the different synthetic routes that are used to prepare Barnidipine hydrochloride.
- The classic synthesis route of Barnidipine hydrochloride involves the reaction of 2,6-diamino-p-quinone with a substituted 1,4-dioxane in the presence of hydrochloric acid and sodium nitrite.
The reaction produces the diacetylene intermediate, which undergoes a sequence of reactions to form the final product. - Another synthetic route involves the reaction of 1,4-dihydro-2,6-dimethyl-p-quinone with a substituted 1,4-dioxane in the presence of a strong base, such as sodium hydride.
The reaction produces the diacetylene intermediate, which undergoes a series of reactions to form the final product. - A modified synthesis route involves the reaction of 2,6-diamino-p-quinone with a substituted 1,4-dioxane in the presence of a coupling agent, such as dicyclohexylcarbodiimide (DCC), and a catalyst, such as hydrochloric acid.
The reaction produces the diacetylene intermediate, which undergoes a series of reactions to form the final product. - A recent synthesis route involves the reaction of 2,6-diamino-p-quinone with a substituted 1,4-dioxane in the presence of a copper catalyst and a base, such as sodium hydroxide.
The reaction produces the diacetylene intermediate, which undergoes a series of reactions to form the final product.
All of these synthesis routes involve the formation of the diacetylene intermediate, which undergoes a series of reactions to form the final product.
The specific reaction conditions and reagents used in each route can vary, but the overall process involves similar steps.
The choice of synthesis route depends on a variety of factors, such as the cost and availability of reagents, the complexity of the synthesis, and the desired yield and purity of the final product.
In conclusion, Barnidipine hydrochloride can be synthesized via several different routes, each with its own advantages and disadvantages.
The choice of synthesis route depends on a variety of factors, such as the cost and availability of reagents, the complexity of the synthesis, and the desired yield and purity of the final product.
Regardless of the synthesis route used, Barnidipine hydrochloride remains an important pharmaceutical drug for the treatment of hypertension and other cardiovascular conditions.