Reacción #1869159

ord-da28e3f72905445186f85e1905136ebe

Ecuación de reacción

O
Water
CCN(CC)CCc1c[nH]c2ccc(NS(=O)(=O)c3ccc4ccccc4c3)cc12
N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]naphthalene-2-sulphonamide
CC(C)(C)[O-].[K+]
potassium t-butoxide
CCI
ethyl iodide
CCN(CC)CCc1c[nH]c2ccc(N(CC)S(=O)(=O)c3ccc4ccccc4c3)cc12
N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]-N-ethyl-naphthalene-2-sulphonamide

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITleft
  2. 2
    workup.STIRRINGwith stirring for 3 hours
  3. 3
    Extracciónis extracted with ethyl acetate
  4. 4
    OtroThe organic solution is evaporated to dryness
  5. 5
    Otrothe resulting crude is purified by chromatography on silica gel

Procedimiento

To a mixture of 285 mg (0.7 mMol) of N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]naphthalene-2-sulphonamide (example 17) and 80 mg (0.7 mMol) of potassium t-butoxide in 3 ml of DMSO are stirred for 30 minutes at ambient temperature. Then are added 105 mg (0.7 mMol) of ethyl iodide and left with stirring for 3 hours. Water is added and is extracted with ethyl acetate. The organic solution is evaporated to dryness and the resulting crude is purified by chromatography on silica gel, using as an eluent mixtures of methylene chloride/methanol/ammonia, yielding N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]-N-ethyl-naphthalene-2-sulphonamide as a solid with m.p.=49-50° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07498328B2uspto-grants-2009_03