Reacción #335653
ord-7db3f1782a7f4e058d8a782fdf36e40b
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturathe mixture was heated in a pressure bottle, under argon at 130°-135° C. for 18 hours
- 2Temperaturacooled
- 3Otroplaced in an ice bath
- 4OtroThe resulting crystals were collected
- 5Lavadowashed with cold pyridine, dichloromethane and ether
- 6Otrorecrystallized from dimethylformamide
Procedimiento
A 3.0 g portion of 2-(5-chloro-3-methylbenzo[b]-thien-2-yl)piperazine was added to 5 ml of pyridine. A 1.01 g portion of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid was added and the mixture was heated in a pressure bottle, under argon at 130°-135° C. for 18 hours, then cooled and placed in an ice bath. The resulting crystals were collected, washed with cold pyridine, dichloromethane and ether and recrystallized from dimethylformamide, giving 401 mg of the desired product, mp 300°-305° C.