Réaction #1869160

ord-e2ceadb7003543839098c55a9adcf662

Équation de réaction

CN1CCC(=O)CC1
1-methyl-4-piperidone
C[O-].[Na+]
sodium methoxide
O=S(=O)(Nc1ccc2[nH]ccc2c1)c1cccc2ccccc12
N-[1H-indol-5-yl]naphthalene-1-sulphonamide
CN1CC=C(c2c[nH]c3ccc(NS(=O)(=O)c4cccc5ccccc45)cc23)CC1
N-[3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]naphthalene-1-sulphonamide
Rendement 52.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe resulting solution is heated
  2. 2
    Températureto reflux for 48 hours
  3. 3
    ConcentrationThe reaction mixture is concentrated at reduced pressure
  4. 4
    Autrethe residue obtained
  5. 5
    Autreis purified by chromatography over silica gel

Mode opératoire

To a solution of 712 mg (13.2 mMol) of sodium methoxide in 100 ml of methanol are added 850 mg (2.64 mMol) of N-[1H-indol-5-yl]naphthalene-1-sulphonamide followed by 596 mg (5.28 mMol) of 1-methyl-4-piperidone and the resulting solution is heated to reflux for 48 hours. The reaction mixture is concentrated at reduced pressure and the residue obtained is purified by chromatography over silica gel, using as eluent mixtures of methylene chloride/methanol/ammonia, to yield 573 mg (52%) of N-[3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]naphthalene-1-sulphonamide as a solid with m.p.=244-245° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07498328B2uspto-grants-2009_03