تفاعل #1869159

ord-da28e3f72905445186f85e1905136ebe

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07498328B2uspto-grants-2009_03