Reaktion #329872

ord-b57d5ff52afe4dbbae5895aac90f5ebb

Reaktionsgleichung

Clc1ccc(Br)cc1
4-chlorobromobenzene
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1
3-(R)-Methyl-piperazine-1-carboxylic acid tert-butyl ester
c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1
BINAP
CC(C)(C)[O-].[Na+]
sodium-t-butoxide
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(Cl)cc1
title compound
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(Cl)cc1
4-(4-Chloro-phenyl)-3-(R)-methyl-piperazine-1-carboxylic acid tert-butyl ester

Lösungsmittel

Reaktionsbedingungen

Temperatur
110°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was evaporated
  2. 2
    Waschenwashed with saturated aqueous sodium bicarbonate and brine
  3. 3
    Trocknendried over magnesium sulfate

Vorschrift

To a mixture of 4-chlorobromobenzene (0.53 g, 2.75 mmol) and 3-(R)-Methyl-piperazine-1-carboxylic acid tert-butyl ester (0.5 g, 2.5 mmol) in toluene (20 mL) was added tris(dibenzylideneacetone) dipalladium(0) (0.029 g, 0.032 mmol), BINAP (0.058 g, 0.093 mmol) and sodium-t-butoxide (1.01 g, 10.5 mmol). The resulting mixture was heated 110° C. for 20 h. The solvent was evaporated and the residue was taken up in ethyl acetate and washed with saturated aqueous sodium bicarbonate and brine and dried over magnesium sulfate. Column chromatography (10% ethyl acetate/hexane) provided the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08653096B2uspto-grants-2014_02