Réaction #218627

ord-122d837db62946b7a7e276c4397ea1a1

Équation de réaction

Cc1cc2c(s1)Nc1cc(F)ccc1NC2=S
6-fluoro-2-methyl-4,9-dihydro-3-thia-4,9-diazabenzo[f]azulene-10-thione
COS(=O)(=O)C(F)(F)F
methyl trifluoromethanesulfonate
COCC[C@H]1CNCCN1
(S)-2-(2-methoxyethyl)piperazine
COCC[C@H]1CN(C2=Nc3ccc(F)cc3Nc3sc(C)cc32)CCN1
(S)-6-Fluoro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulene

Conditions de réaction

Température
90°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurecool in an ice/water bath
  2. 2
    ConcentrationConcentrate the reaction mixture under reduced pressure
  3. 3
    workup.STIRRINGstir the reaction mixture under nitrogen
  4. 4
    ConcentrationConcentrate the reaction mixture under reduced pressure
  5. 5
    Autrepurify by flash column chromatography on silica gel (eluent dichloromethane/methanol)
  6. 6
    Autreto give the

Mode opératoire

Suspend 6-fluoro-2-methyl-4,9-dihydro-3-thia-4,9-diazabenzo[f]azulene-10-thione (500 mg, 1.9 mmol) in dichloromethane (30 ml), stir under nitrogen and cool in an ice/water bath. Add methyl trifluoromethanesulfonate (500 μl), and stir overnight. Concentrate the reaction mixture under reduced pressure, take up in pyridine (10 ml) and add (S)-2-(2-methoxyethyl)piperazine (400 mg, 2.78 mmol) and stir the reaction mixture under nitrogen and heat at 90° C. for three days. Concentrate the reaction mixture under reduced pressure and purify by flash column chromatography on silica gel (eluent dichloromethane/methanol) to give the desired as a yellow solid 727 mg: Mass Spectrum (FIA) 375 (M+1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07384934B2uspto-grants-2008_06