Reaktion #57279

ord-7e3f5a82c4654e8ca0222ca8d720a2d1

Reaktionsgleichung

Clc1ncc(Br)cn1
5-bromo-2-chloropyrimidine
CC(C)(C)OC(=O)N1CCNCC1
1,1-dimethylethyl 1-piperazinecarboxylate
CC(C)(C)OC(=O)N1CCN(c2ncc(Br)cn2)CC1
title compound
Ausbeute 58.0%
CC(C)(C)OC(=O)N1CCN(c2ncc(Br)cn2)CC1
1,1-dimethylethyl 4-(5-bromo-2-pyrimidinyl)-1-piperazinecarboxylate
Ausbeute 58.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux for 2 hours
  3. 3
    SonstigeSeparation of the organic layer
  4. 4
    Sonstigedrying
  5. 5
    Filtration(MgSO4), filtration and concentration in vacuo
  6. 6
    Sonstigeprovided a residue which
  7. 7
    Sonstigewas purified by silica gel chromatography (40 g silica gel, CHCl3/EtOAc)

Vorschrift

A mixture of 5-bromo-2-chloropyrimidine (5.17 mmol) and 1,1-dimethylethyl 1-piperazinecarboxylate (11.4 mmol) in 1,4-dioxane (10 ml) was heated at reflux for 2 hours. After cooling to room temperature, the reaction mixture was diluted with water (100 ml) and ethyl acetate (100 ml). Separation of the organic layer, drying (MgSO4), filtration and concentration in vacuo provided a residue which was purified by silica gel chromatography (40 g silica gel, CHCl3/EtOAc) to give the title compound as a white solid (58%). ESMS [M+H-Boc]+: 245.0/243.0.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07419988B2uspto-grants-2008_09