-
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
2,6-Dichloro-4-pyrimidinamine is an important intermediate in the synthesis of various pharmaceuticals and other chemical products.
It is a white or almost white crystalline solid with a melting point of around 160-162°C.
The structure of 2,6-dichloro-4-pyrimidinamine is shown below:
The synthesis of 2,6-dichloro-4-pyrimidinamine can be achieved through several different routes, including the following:
- Hydrochlorination of 4-amino-2,6-dichloropyrimidine:
This reaction involves the conversion of 4-amino-2,6-dichloropyrimidine, which is treated with hydrogen chloride gas in the presence of a catalyst such as aluminum chloride.
The reaction is exothermic and requires careful monitoring to avoid excessive heat buildup.
- Diazotization of 4-chloro-2,6-dichloropyrimidine:
This method involves the conversion of 4-chloro-2,6-dichloropyrimidine, which is treated with sodium nitrite and hydrochloric acid.
The resulting compound is then treated with a solution of ammonia and hydrochloric acid, which converts it to 2,6-dichloro-4-pyrimidinamine.
- Chlorination of 4-aminopyrimidine:
This method involves the conversion of 4-aminopyrimidine, which is treated with chlorine gas in the presence of a catalyst such as iron(III) chloride.
The reaction is exothermic and requires careful monitoring to avoid excessive heat buildup.
- Nitration of 4-aminopyrimidine:
This method involves the conversion of 4-aminopyrimidine, which is treated with nitric acid.
The resulting compound is then treated with a solution of sodium hydroxide, which converts it to 2,6-dichloro-4-pyrimidinamine.
The choice of synthesis route depends on various factors, such as the availability of reagents, the cost of the reaction, and the desired yield of the product.
The synthesis of 2,6-dichloro-4-pyrimidinamine via any of these routes is a complex and multistep process that requires careful attention to detail and the use of appropriate safety precautions.
The resulting product must be thoroughly purified and characterized to ensure its identity and purity.
In conclusion, the synthesis of 2,6-dichloro-4-pyrimidinamine is an important process in the pharmaceutical and chemical industries, and several different synthesis routes are available.
The choice of route depends on various factors, and the process requires careful attention to detail and appropriate safety precautions.
The resulting product must be thoroughly purified and characterized to ensure its identity and purity.