Réaction #6674

ord-aab5b1b567764967a3b9eb9b16000b36

Équation de réaction

[K+].[OH-]
potassium hydroxide
O=P(Cl)(Cl)Cl
Phosphorus oxychloride
CN(C)C=O
dimethylformamide
CCN1c2ccccc2Sc2ccccc21
10-ethylphenothiazine
CN(C)C=O
DMF
CCN1c2ccccc2Sc2cc(C=O)ccc21
10-Ethylphenothiazine-3-carbaldehyde

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was refluxed at 80° C. for 24 hours
  2. 2
    ExtractionThe product was extracted with chloroform
  3. 3
    ExtractionThe chloroform extract
  4. 4
    Séchagewas dried with anhydrous sodium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    workup.DISTILLATIONdistilled
  7. 7
    AutreThe product was crystallized from methanol

Mode opératoire

Phosphorus oxychloride (POCl3,3.7 ml, 0.04 mol) was added dropwise to 4.4 ml (0.06 mol) of dry dimethylformamide (DMF) at 0° C. under a nitrogen atmosphere. This solution was warmed up slowly to room temperature. Then, a solution of 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise. The reaction mixture was refluxed at 80° C. for 24 hours and poured into the ice water. This solution was neutralized with potassium hydroxide until the pH reached 6–8. The product was extracted with chloroform. The chloroform extract was dried with anhydrous sodium sulfate, filtered and distilled. The product was crystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde (C15H13NOS, FW=255.34) was 65%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07083884B2uspto-grants-2006_08