-
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
N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide is a compound that is widely used in various chemical reactions and synthesis processes.
The compound is a synthetic intermediate that can be used to produce other chemicals and pharmaceuticals.
One of the most common techniques used to synthesize N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide is through a two-step synthesis process.
The first step involves the synthesis of N-ethyl-2-chloropyridine-4-carboxamide, which is a similar compound to N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide.
The synthesis of N-ethyl-2-chloropyridine-4-carboxamide is typically carried out by reacting ethyl acetate with chlorpyridine in the presence of a solvent such as water or methanol.
The reaction is then followed by the reduction of the nitro group to form the carboxamide.
The second step involves the synthesis of N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide by reacting N-ethyl-2-chloropyridine-4-carboxamide with benzyl amine in the presence of a catalyst such as sodium hydroxide.
This reaction is typically carried out in a solvent such as toluene or xylene.
An alternative synthesis route for N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide is through the reaction of N-ethyl-2-chloropyridine-4-carboxamide with benzyl chloride in the presence of a Lewis acid catalyst such as aluminum chloride.
The reaction can be carried out at a temperature range of 80-100°C in a suitable solvent such as toluene or xylene.
Another synthesis route for N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide involves the reaction of N-ethyl-2-chloropyridine-4-carboxamide with benzaldehyde in the presence of a condensation agent such as p-toluenesulfonyl chloride.
The reaction is typically carried out in a solvent such as toluene or xylene, and can be followed by further reaction with sodium hydroxide to form the carboxamide.
In addition to the above synthesis routes, N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide can also be synthesized through other methods, such as through the reduction of N-ethyl-2-chloro-6-nitro-pyridine-4-carboxamide or through the reaction of N-ethyl-2-chloro-pyridine-4-carboxamide with benzyl bromide.
The synthesis of N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide is an important step in the production of various chemicals and pharmaceuticals.
The compound can be used as an intermediate in the synthesis of other chemicals, or as an active ingredient in pharmaceuticals.
One application of N-benzyl-2-chloro-N-ethylpyridine-4-carboxamide is in the production of antihistamines and antiallergic drugs.
It can also be used as a starting material in the production of herbicides and pesticides.
In the pharmaceutical industry, N-benzyl-2-chloro-