Reacción #2358521

ord-c486dd16e6c14a00b2e48518359803fe

Ecuación de reacción

ClCCl
CH2Cl2
CS(=O)(=O)c1cc(F)cc(OCCBr)c1
1-(2-bromoethoxy)-3-fluoro-5-methylsulfonyl-benzene
C1CNC1
azetidine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CS(=O)(=O)c1cc(F)cc(OCCN2CCC2)c1
1-[2-(3-fluoro-5-methylsulfonyl-phenoxy)ethyl]azetidine

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was cooled to room temperature
  2. 2
    Filtraciónsolids was filtered off
  3. 3
    Otrothe volatiles were evaporated
  4. 4
    Otrore-crystallized from methanol/diethyl ether

Procedimiento

1-(2-bromoethoxy)-3-fluoro-5-methylsulfonyl-benzene (0.5 g, 1.6 mmol), azetidine (0.23 ml, 3.2 mmol) and potassium carbonate (0.58 g, 4.2 mmol) was dissolved in acetonitrile (10 ml). The mixture was heated in a sealed container at 120° C. for 2 h. The reaction mixture was cooled to room temperature, CH2Cl2 (100 ml) was added, solids was filtered off and the volatiles were evaporated. The amine was converted to the fumaric acid salt and re-crystallized from methanol/diethyl ether. MS m/z (relative intensity, 70 eV) 273 (M+, 1), 94 (5), 82 (3), 71 (5), 70 (bp).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09120728B2uspto-grants-2015_09