반응 #1869159

ord-da28e3f72905445186f85e1905136ebe

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07498328B2uspto-grants-2009_03