An Efficient and Novel Synthesis of Fused Thiazol-2(3H)-ones

Autor: Page Donald Frederick, Bacon Edward R, George Y. Lesher, Baldev Singh, Patrick O. Pennock
Rok vydání: 1993
Předmět:
Zdroj: HETEROCYCLES. 36:133
ISSN: 0385-5414
DOI: 10.3987/com-92-6193
Popis: Reaction of o-bromo aromatic amines (2, 4, 7, 10, 15) with ethyl potassium xanthate gave the corresponding fused thiazol-2(3H)-thiones (16, 19, 22) which in turn were first alkylated with methyl iodide and then treated with sodium methoxide to produce fused thiazol-2(3H)-ones (18, 21, 24). Treatment of 4-(4-pyridinyl)-benzenamine dihydrobromide (1) with DMSO gave 2-bromo-4-(4-pyridinyl)benzenamine (2). Reduction of 4-(4-bromo-3-nitrophenyl)-pyridine (3) with stannous chloride gave 2-bromo-5-(4-pyridinyl)-benzenamine (4)
Databáze: OpenAIRE