Reaktion #11727

ord-560be2081f054067815e1cc2c2faf8c2

Reaktionsgleichung

O=C(Cl)CCl
chloroacetyl chloride
C[C@@H]1CN[C@@H](C)CN1Cc1ccc(F)cc1
(2R,5S)-1-(4-fluoro-benzyl)-2,5-dimethyl-piperazine
CCN(CC)CC
triethylamine
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)CCl
title compound
Ausbeute 84.9%
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)CCl
2-Chloro-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanone
Ausbeute 84.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe resulting reaction mixture
  2. 2
    FiltrationThe reaction was then filtered through a pad of celite
  3. 3
    Waschenwashed with dichloromethane
  4. 4
    Einengenthe resulting filtrate was concentrated

Vorschrift

To a solution of (2R,5S)-1-(4-fluoro-benzyl)-2,5-dimethyl-piperazine (2.5 g, 11.2 mmol) in dry dichloromethane (11 mL) at 0° C. was added triethylamine (1.57 mL, 11.2 mmol) followed by chloroacetyl chloride (0.86 mL, 11.2 mmol). The resulting reaction mixture was stirred for 30 minutes. The reaction was then filtered through a pad of celite, washed with dichloromethane and the resulting filtrate was concentrated. Chromatography on silica gel gave the title compound (2.84 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07098212B2uspto-grants-2006_08