Synthetic Route of 52415-29-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.52415-29-9, Name is 6-Bromoindole, molecular formula is C8H6BrN. In a Article，once mentioned of 52415-29-9
A Bronsted acid catalyzed bisindolization reaction with suitable alpha-amido acetals that tolerates a wide range of indoles is reported. The method allows rapid access to the biologically relevant bisindolyl ethanamine scaffold in good to excellent yields upon mild amide basic hydrolysis. In preliminary pharmacological studies, some of these compounds display cytotoxic activity in U937 cancer cells. The marine natural alkaloid 2,2-di(6?- bromo-3?-indolyl)-ethylamine was the most active compound and could be a lead candidate for further optimization. For the first time, the biological role of this brominated bisindole marine alkaloid is presented. Bronsted acid catalyzed reaction of indoles with (acylamino)acetaldehyde dimethyl acetal efficiently affords bis(indolyl)ethanamino derivatives. The dibrominated marine natural product bisindole alkaloid 1 showed potent anticancer activity against U937 cells. Copyright
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 52415-29-9
Reference：
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles