Reaktion #68982

ord-1a01cbea3570408d92ecb309f9d6eb9a

Reaktionsgleichung

CC(C)(C)[O-].[Na+]
sodium t-butoxide
CC(C)(C)OC(=O)N1C2CCC1CN(c1ccc(Br)cc1)C2
3-(4-Bromophenyl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester
CS(=O)(=O)N1CCNCC1
1-methanesulfonylpiperazine
COc1cccc(OC)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1
S-Phos
CC(C)(C)OC(=O)N1C2CCC1CN(c1ccc(N3CCN(S(C)(=O)=O)CC3)cc1)C2
3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[3.2.1]-octane-8-carboxylic acid tert-butyl ester
Ausbeute 97.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 1 h 30
  2. 2
    SonstigeAfter hydrolysis
  3. 3
    Extraktionwith a saturated aqueous NaHCO3 solution, and extraction with ethyl acetate
  4. 4
    Waschenthe organic phase is washed with a saturated aqueous sodium chloride solution
  5. 5
    Trocknendried over MgSO4
  6. 6
    SonstigeThe crude product obtained
  7. 7
    Sonstigeis chromatographed on silica gel, elution

Vorschrift

3-(4-Bromophenyl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (0.64 g, 1.7 mmol), 1-methanesulfonylpiperazine (0.43 g, 2.6 mmol), tris-(dibenzylideneacetone)dipalladium (0.069 g, 0.07 mmol), S-Phos (0.11 g, 0.28 mmol), and sodium t-butoxide (0.25 g, 2.6 mmol) are placed in 10 ml of toluene under nitrogen. The reaction medium is stirred at reflux for 1 h 30. After hydrolysis with a saturated aqueous NaHCO3 solution, and extraction with ethyl acetate, the organic phase is washed with a saturated aqueous sodium chloride solution and dried over MgSO4. The crude product obtained is chromatographed on silica gel, elution being carried out with a gradient of methanol/ethyl acetate in dichloromethane ranging from 100/0/0 to 7/2.5/0.5 (dichloromethane/ethyl acetate/methanol). 0.75 g of expected 3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[3.2.1]-octane-8-carboxylic acid tert-butyl ester is obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530477B2uspto-grants-2013_09