Reacción #86562

ord-c8efbae1e7e5415e9dca6356f393c41d

Ecuación de reacción

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O
water
Cc1csc2nc(C(C)N=[N+]=[N-])c(Br)c(=O)n12
7-(1-azidoethyl)-6-bromo-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one
Cc1ccc(B(O)O)cc1
(4-methylphenyl)boronic acid
Cc1ccc(-c2c(C(C)N=[N+]=[N-])nc3scc(C)n3c2=O)cc1
desired product
Rendimiento 61.5%
Cc1ccc(-c2c(C(C)N=[N+]=[N-])nc3scc(C)n3c2=O)cc1
7-(1-azidoethyl)-3-methyl-6-(4-methylphenyl)-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one
Rendimiento 61.5%

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling to room temperature
  2. 2
    Lavadowashed with water
  3. 3
    Secadodried over MgSO4
  4. 4
    Concentraciónconcentrated
  5. 5
    Otropurified on silica gel (0-25% ethyl acetate/hexane)

Procedimiento

To a mixture of 7-(1-azidoethyl)-6-bromo-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.080 g, 0.25 mmol) and (4-methylphenyl)boronic acid (0.042 g, 0.31 mmol) in 1,4-dioxane (2 mL) was added 1 N solution of sodium carbonate in water (0.38 mL, 0.38 mmol) and dichloro(bis{di-tert-butyl[4-(dimethylamino)phenyl]phosphoranyl})palladium (0.011 g, 0.015 mmol). The mixture was heated at 100° C. overnight. After cooling to room temperature, the mixture was diluted with ethyl acetate, washed with water, dried over MgSO4, concentrated and then purified on silica gel (0-25% ethyl acetate/hexane) to give the desired product (50 mg). LCMS calculated for C16H16N5OS (M+H)+: m/z=326.1. Found: 326.0.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09434746B2uspto-grants-2016_09