Réaction #2320117

ord-0beeca0d01a243c7b6cc5bfde4ad7ea1

Équation de réaction

COc1ccc(Br)cc1S(C)(=O)=O
4-bromo-2-methanesulfonyl-1-methoxy-benzene
C1CNCCN1
piperazine
CC(C)(C)[O-].[Na+]
sodium tert-butoxide
COc1ccc(N2CCNCC2)cc1S(C)(=O)=O
1-(3-Methanesulfonyl-4-methoxy-phenyl)-piperazine

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed with brine (15-20 ml)
  2. 2
    SéchageThe organic fraction was dried (MgSO4)
  3. 3
    Filtrationfiltered
  4. 4
    Autreevaporated to dryness
  5. 5
    AutreThe crude material was purified by flash chromatography on silica gel

Mode opératoire

A mixture of 4-bromo-2-methanesulfonyl-1-methoxy-benzene (0.65 g,), piperazine (0.43 g,), sodium tert-butoxide (0.13 g) BINAP (19 mg) and [Pd2(dba)3 (27 mg) in dioxane (5 ml) was heated under argon at 100° C. for 24 h. After cooling to room temperature, the reaction mixture was taken up in Et2O (40-50 ml) and washed with brine (15-20 ml). The organic fraction was dried (MgSO4), filtered and evaporated to dryness. The crude material was purified by flash chromatography on silica gel using CH2Cl2:MeOH (9:1 (v/v)) Yield 0.14 g: MS m/z (rel. intensity, 70 eV)) 270 (M+, 23), 229 (11), 228 (bp), 148 (7), 56 (17).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE041315E1uspto-grants-2010_05