-
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
5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine, also known as Br-Cl-PyPyr, is a synthetic compound that is used in various industrial applications.
This compound is commonly used as a building block for the synthesis of other organic compounds, medications, and materials.
The synthetic routes to Br-Cl-PyPyr can vary, and in this article, we will discuss some of the most commonly used methods.
One of the most common methods for the synthesis of Br-Cl-PyPyr is through the reaction of 4-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine with hydroxylamine.
This reaction results in the formation of the desired compound, with a yield of up to 90%.
The reaction typically takes place in the presence of an organic solvent, such as DMF, and is often carried out at room temperature.
Another common synthetic route for Br-Cl-PyPyr is through the reaction of 4-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine with malonic acid diester.
This reaction is carried out in the presence of a Lewis acid catalyst, such as aluminum chloride, and is typically performed at an elevated temperature, such as 80-90°C.
The yield of the reaction can be up to 85%.
A third synthetic route for Br-Cl-PyPyr is through the reaction of 4-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine with glyoxal.
This reaction is typically carried out in an aqueous solution, and is often performed at a pH of around 7.
The reaction is typically completed in the presence of a catalyst, such as pyridine, and can yield up to 80% of the desired compound.
In addition to these synthetic routes, Br-Cl-PyPyr can also be synthesized through other methods, such as Suzuki-Miyaura cross-coupling and Stille coupling.
These methods offer different advantages and disadvantages, and the choice of synthetic route may depend on the specific application and the desired yield.
Overall, the synthetic routes to 5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine are numerous, and the choice of route may depend on the specific application and the desired yield.
The three routes discussed in this article are just a few of the many methods that are available for the synthesis of this compound.
