-
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
4-Isoquinolinamine is an important organic compound used in a variety of applications in the chemical industry.
It is a precursor to a number of pharmaceutical agents, agrochemicals, and intermediates for the production of dyes, polymers, and other chemical products.
The synthesis of 4-isoquinolinamine can be achieved through several routes, including synthetic routes, medicinal routes, and so on.
In this article, we will focus on the synthetic routes to 4-isoquinolinamine.
The earliest synthetic route to 4-isoquinolinamine involved the reaction of salicylic aldehyde with furfuraldehyde in the presence of sodium hydroxide.
This reaction leads to the formation of a hemiaminal intermediate, which undergoes dehydration to form the desired 4-isoquinolinamine.
However, this route has a number of drawbacks, including the necessity of using toxic reagents such as sodium hydroxide and the generation of large amounts of waste.
A more recent synthetic route to 4-isoquinolinamine involves the reaction of aniline with o-phenylenediamine in the presence of a Lewis acid catalyst such as aluminum chloride.
This reaction leads to the formation of the desired 4-isoquinolinamine after hydrolysis of the resulting imine.
This route is more environmentally friendly than the earlier synthetic routes, as it does not require the use of toxic reagents.
Another synthetic route to 4-isoquinolinamine involves the reaction of aniline with azo compounds such as o-nitroaniline.
This reaction leads to the formation of azoanilides, which can be hydrolyzed to form 4-isoquinolinamine.
This route is also environmentally friendly, as it does not require the use of toxic reagents.
Medicinal routes to 4-isoquinolinamine also exist, such as the synthesis of the compound from tryptamine and a number of other reagents.
However, these routes are less commonly used in industry due to the lack of efficiency and the high cost of the reagents involved.
In conclusion, 4-isoquinolinamine is an important organic compound used in a variety of applications in the chemical industry.
Synthetic routes to the compound include the reaction of salicylic aldehyde with furfuraldehyde, the reaction of aniline with o-phenylenediamine in the presence of a Lewis acid catalyst, and the reaction of aniline with azo compounds such as o-nitroaniline.
These routes offer advantages in terms of efficiency and environmental friendliness.