Reacción #1747859
ord-d521502a280947329879582b45a2df58
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroprepared analogously to Example 13 in U.S
- 2Otrorose from 25 to 43° C
- 3workup.STIRRINGstirred for 15 min
- 4Filtraciónfiltered through a black band
- 5Filtraciónfilter
- 6LavadoThe residue was washed with 300 ml of methanol
- 7Otrodried at 80° C. under reduced pressure
- 8workup.DISSOLUTIONThe crude product (4.7 g) was dissolved in 150 ml of methylene chloride
- 9Otropurified on silica gel
- 10Otrorecrystallized from 83 ml of butylglycol
- 11Otrowere obtained
Procedimiento
3.46 g (30.4 mmol) of potassium tert-butoxide and then 3.60 g (13.4 mmol) of 10-methylphenothiazine-3,7-dicarbaldehyde were added with stirring and at room temperature to a solution of 8.20 g (26.8 mmol) of diethyl benzhydrylphosphonate (prepared analogously to Example 13 in U.S. Pat. No. 5,130,603) in 60 ml of anhydrous dimethyl sulfoxide, in the course of which the temperature rose from 25 to 43° C. After stirring at room temperature for 5 hours, the reaction solution was admixed with 150 ml of methanol, stirred for 15 min and filtered through a black band filter. The residue was washed with 300 ml of methanol and dried at 80° C. under reduced pressure. The crude product (4.7 g) was dissolved in 150 ml of methylene chloride, purified on silica gel and recrystallized from 83 ml of butylglycol. 3.56 g (23% of theory) of greenish microcrystals having a melting point of 233-241° C. were obtained.