Simple exploration of 15864-32-1

15864-32-1, As the paragraph descriping shows that 15864-32-1 is playing an increasingly important role.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.15864-32-1,2-Amino-6-bromobenzothiazole,as a common compound, the synthetic route is as follows.

To a solution of commercially available 2-amino-6-bromobenzothiazole (3.0 g, 13.0 mmol) in THF (30 mL) was added acetic anhydride (4 mL, 42.3 mmol). The solution was stirred at room temperature for 2 days. THF was removedin vacuoand the residue was recrystallized from hot EtOAc to giveN-(6-bromobenzo[d]thiazol-2-yl)acetamide (2.5 g, 71%).

15864-32-1, As the paragraph descriping shows that 15864-32-1 is playing an increasingly important role.

Reference：
Article; Pecchi, Sabina; Ni, Zhi-Jie; Han, Wooseok; Smith, Aaron; Lan, Jiong; Burger, Matthew; Merritt, Hanne; Wiesmann, Marion; Chan, John; Kaufman, Susan; Knapp, Mark S.; Janssen, Johanna; Huh, Kay; Voliva, Charles F.; Bioorganic and Medicinal Chemistry Letters; vol. 23; 16; (2013); p. 4652 – 4656;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica