-
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-Tosyl-5-bromo-4,7-diazaindole is an important intermediate in the synthesis of various drugs, agrochemicals, and other chemical products.
The synthesis of this compound has been extensively studied in the chemical industry, and several synthetic routes have been developed to produce this compound in high yield and purity.
One of the most common synthetic routes for N-Tosyl-5-bromo-4,7-diazaindole involves the reaction of 5-bromo-2-nitrobenzoxazole with sodium nitrite and tosyl chloride in the presence of a solvent such as benzene or toluene.
The reaction proceeds through a series of steps, including the formation of a nitro group, a diazo group, and finally the tosylated product.
Another synthetic route involves the reaction of 2-nitro-5-bromobenzoic acid with sodium nitrite in the presence of anhydrous sodium carbonate.
The reaction is carried out in an alcohol solvent such as methanol or ethanol, and the produced N-Tosyl-5-bromo-4,7-diazaindole can be isolated by filtration and washing with water.
A third synthetic route involves the reaction of 5-bromo-2-nitrobenzaldehyde with tosyl chloride in the presence of an acid catalyst such as hydrochloric acid.
The reaction is carried out in a suitable solvent such as acetone or dichloromethane, and the produced N-Tosyl-5-bromo-4,7-diazaindole can be isolated by filtration and washing with water.
Regardless of the synthetic route used, the purity and yield of N-Tosyl-5-bromo-4,7-diazaindole can be further improved through various purification methods such as crystallization, distillation, and chromatography.
The synthetic routes to N-Tosyl-5-bromo-4,7-diazaindole are various and the choice of a specific route depends on the availability of the starting materials and the desired yield and purity of the final product.
The advantages and disadvantages of each synthetic route must be carefully considered before making a decision on which route to use.
In conclusion, N-Tosyl-5-bromo-4,7-diazaindole is an important intermediate in the synthesis of various drugs, agrochemicals, and other chemical products, and the synthesis of this compound has been extensively studied in the chemical industry.
Several synthetic routes have been developed to produce N-Tosyl-5-bromo-4,7-diazaindole in high yield and purity, including the reaction of 5-bromo-2-nitrobenzoxazole with sodium nitrite and tosyl chloride in the presence of a solvent such as benzene or toluene, the reaction of 2-nitro-5-bromobenzoic acid with sodium nitrite in the presence of anhydrous sodium carbonate, and the reaction of 5-bromo-2-nitrobenzaldehyde with tosyl chloride in the presence of an acid catalyst such as hydrochloric acid.
The purity and yield of N-Tosyl-5-bromo-4,7-diazaindole can be further improved through various purification methods such as crystallization, distillation, and chromatography.