反应 #1869159

ord-da28e3f72905445186f85e1905136ebe

反应方程式

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

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

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

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07498328B2uspto-grants-2009_03