Réaction #1747871

ord-1b749d67acf84475b4e75548439ac5cc

Équation de réaction

Cc1cc(C)c(N2c3ccccc3Sc3ccccc32)c(C)c1
10-mesitylphenothiazine
CN(C=O)c1ccccc1
N-methylformanilide
O=P(Cl)(Cl)Cl
phosphorus oxychloride
CC(=O)[O-].[Na+]
sodium acetate
Cc1cc(C)c(N2c3ccccc3Sc3cc(C=O)ccc32)c(C)c1
10-Mesitylphenothiazine-3-carbaldehyde

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGAfter stirring at 20° C. for 30 min
  2. 2
    workup.STIRRINGAfter stirring at 70° C. for 1 hour
  3. 3
    AutreN-methylformanilide and o-dichlorobenzene were removed with a steam distillation
  4. 4
    workup.ADDITION250 ml of methylene chloride were added to the distillation bottoms
  5. 5
    AutreThe organic phase was removed
  6. 6
    Filtrationfiltered through silica gel
  7. 7
    ConcentrationThe filtrate was concentrated
  8. 8
    Autredried at 40° C. under reduced pressure
  9. 9
    Autrewere obtained

Mode opératoire

3.66 g (23.6 mmol) of 99% phosphorus oxychloride were added dropwise at 20° C. with stirring and ice cooling to a solution of 5.00 g (15.8 mmol) of 10-mesitylphenothiazine and 3.23 g (23.6 mmol) of 99% N-methylformanilide in 5 ml of o-dichlorobenzene within 15 min. After stirring at 20° C. for 30 min, the reaction solution was heated to 70° C. and kept at this temperature for 4 hours. The reaction solution was admixed with a solution of 16 g of sodium acetate in 35 ml of water within 5 min. After stirring at 70° C. for 1 hour, N-methylformanilide and o-dichlorobenzene were removed with a steam distillation. 250 ml of methylene chloride were added to the distillation bottoms. The organic phase was removed and filtered through silica gel. The filtrate was concentrated and dried at 40° C. under reduced pressure. 5.05 g (93% of theory) of analytically pure greenish powder having a melting point of 136-140° C. were obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08029919B2uspto-grants-2011_10