Reacción #573325

ord-204d51bdd6724740948056486a36a761

Ecuación de reacción

O=C(O)c1ccc(Br)s1
5-bromo-2-thiophenecarboxylic acid
O=S(Cl)Cl
thionyl chloride
O=C(Cl)c1ccc(Br)s1
5-bromo-2-thiophenecarbonyl chloride

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Following the procedure of Example 32, 2.07 g (10.0 mmoles) of commercially available 5-bromo-2-thiophenecarboxylic acid was reacted with 10 ml of thionyl chloride to give 2.35 g of crude 5-bromo-2-thiophenecarbonyl chloride as a red oil. The total crude acid chloride was coupled to 1.76 g (8.33 mmoles) of 5-chloro-2-oxindole-1-carboxamide by the procedure in Example 32 using 3.05 g (25.0 mmoles) of 4-(N,N-dimethylamino)pyridine and 50 ml of N,N-dimethylformamide. Acidic workup gave a solid which was recrystallized to give 1.77 g (4.43 mmoles, 53% yield) of title compound as reddish-brown crystals, m.p. 228°-229° C. (tetrahydrofuran).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05290802uspto-grants-1994_03