Reacción #3584
ord-c90afcddae0140da8c78ba26df0ff270
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONis added
- 2OtroThe cooling bath is removed and after about 30 minutes a complete solution
- 3Otrois obtained
- 4workup.STIRRINGto stir at room temperature for 48 hours
- 5Concentraciónthe volatiles are concentrated in vacuo to a residue
- 6workup.DISSOLUTIONThe residue is dissolved in 100 ml of ethyl acetate
- 7Lavadowashed with water, 2N citric acid, aqueous NaHCO3 and brine
- 8SecadoThe solution is dried with Na2SO4
- 9Concentraciónthe volatiles concentrated in vacuo
Procedimiento
To a mixture of 1.93 g of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 15 ml of methylene chloride, cooled to 0° C. is added 1.13 ml of triethylamine. After stirring for 3 minutes, a mixture of 1.0 g of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 5 ml of methylene chloride is added. The cooling bath is removed and after about 30 minutes a complete solution is obtained. The reaction mixture is allowed to stir at room temperature for 48 hours and the volatiles are concentrated in vacuo to a residue. The residue is dissolved in 100 ml of ethyl acetate and washed with water, 2N citric acid, aqueous NaHCO3 and brine. The solution is dried with Na2SO4 and the volatiles concentrated in vacuo to give 3.0 g of a residue. A 300 mg sample of the residue is purified by thick layer chromatography using 10% ethyl acetate-methylene chloride to give 160 mg of the desired product. The remainder of the crude material is purified by flash chromatography using 10% ethyl acetate in methylene chloride to give the desired product as a residue which is crystallized from ethyl acetate to give 800 mg of the desired product as white crystals, m.p. 212°-215° C.