Réaction #1857589

ord-07afc07c0aec4f2f827fd5473d6d55ab

Équation de réaction

O=C(O)Cn1nc(C(F)F)cc1C(F)F
[3,5-bis-(difluoromethyl)-1H-pyrazol-1-yl]acetic acid
O=C(Cl)C(=O)Cl
oxalyl chloride
O=C([O-])O.[Na+]
sodium hydrogencarbonate
O=Cc1cccc(F)c1C1CC(c2csc(C3CC[NH2+]CC3)n2)=NO1.[Cl-]
4-{4-[5-(2-fluoro-6-formylphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidinium chloride
CCN(CC)CC
triethylamine
O=Cc1cccc(F)c1C1CC(c2csc(C3CCN(C(=O)Cn4nc(C(F)F)cc4C(F)F)CC3)n2)=NO1
2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-fluorobenzaldehyde

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe solvent and the excess reagent were removed under reduced pressure
  2. 2
    workup.DISSOLUTIONThe solid residue was again dissolved in dichloromethane (5 ml) and, at 0° C.
  3. 3
    workup.STIRRINGThe reaction mixture was stirred at room temperature overnight
  4. 4
    Autrethe aqueous phase was removed
  5. 5
    Extractionextracted with ethyl acetate
  6. 6
    SéchageThe combined organic phases were dried over sodium sulphate
  7. 7
    Concentrationconcentrated
  8. 8
    AutrePurification by column chromatography

Mode opératoire

To a solution of [3,5-bis-(difluoromethyl)-1H-pyrazol-1-yl]acetic acid (58 mg) in dichloromethane (20 ml) were added, at 0° C., oxalyl chloride (94.5 mg) and one drop of N,N-dimethylformamide. The reaction mixture was stirred at room temperature for 2 hours. The solvent and the excess reagent were removed under reduced pressure. The solid residue was again dissolved in dichloromethane (5 ml) and, at 0° C., added dropwise to a solution of 4-{4-[5-(2-fluoro-6-formylphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidinium chloride and triethylamine (5.0 eq.) in dichloromethane (15 ml). The reaction mixture was stirred at room temperature overnight. Then it was admixed with concentrated sodium hydrogencarbonate solution, and the aqueous phase was removed and extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated. Purification by column chromatography gave 2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-fluorobenzaldehyde (55 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09247748B2uspto-grants-2016_02