-
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
6-Chloro-2-ethoxy-4-pyrimidinamine is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products.
The synthesis of this compound can be achieved through several routes, including synthetic routes.
In this article, we will discuss some of the most common synthetic routes for the synthesis of 6-chloro-2-ethoxy-4-pyrimidinamine.
- Route 1: via 2-Chloro-4-nitro-5-ethoxy-6-pyrimidine
The first synthetic route for the synthesis of 6-chloro-2-ethoxy-4-pyrimidinamine involves the synthesis of 2-chloro-4-nitro-5-ethoxy-6-pyrimidine, followed by reduction of the nitro group to an amine.
The reaction scheme is shown below:
Here, Cl-C6H4-CH2CH2-N-CH2CH2N-C6H4-Cl (1) is treated with sodium hydroxide and the resulting nitroso compound is reduced with hydrazine to yield the desired amine (2).
This amine is then chlorinated with chloroform to give the desired product (3).
- Route 2: via 2-Amino-5-ethoxy-6-pyrimidine
Another synthetic route for the synthesis of 6-chloro-2-ethoxy-4-pyrimidinamine involves the synthesis of 2-amino-5-ethoxy-6-pyrimidine, followed by chlorination of the amine group.
The reaction scheme is shown below:
Here, 2-amino-5-ethoxy-6-pyrimidine (4) is treated with chloroform and the resulting chloramine is chlorinated with chloroform to yield the desired product (5).
- Route 3: via 6-Chloro-2-methoxy-4-pyrimidine
A third synthetic route for the synthesis of 6-chloro-2-ethoxy-4-pyrimidinamine involves the synthesis of 6-chloro-2-methoxy-4-pyrimidine, followed by ethoxylation of the methoxy group.
The reaction scheme is shown below:
Here, Cl-C6H4-CH2OCH3 (6) is treated with sodium hydroxide and the resulting methoxide is treated with ethyl bromide to yield the desired ethoxy compound (7).
In conclusion, the synthesis of 6-chloro-2-ethoxy-4-pyrimidinamine can be achieved through several synthetic routes, including the routes outlined above.
Each of these routes has its own advantages and disadvantages, and the choice of route will depend on factors such as the availability of starting materials, the desired yield, and the specific requirements of the final product.
Regardless of the route chosen, the synthesis of 6-chloro-2-ethoxy-4-pyrimidinamine is an important and valuable synthetic transformation in the chemical industry.