Reaktion #78849

ord-a28cba4d344a4cdb91c299195a232b19

Reaktionsgleichung

Brc1cncc(Br)c1
3,5-dibromopyridine
c1ccc(P(c2ccccc2)c2ccccc2)cc1
PPh3
[Cl-].[Zn+][c]1ccccn1
2-pyridinyl zinc chloride
Brc1cncc(-c2ccccn2)c1
title compound
Brc1cncc(-c2ccccn2)c1
3-Bromo-5-(2-pyridinyl)-pyridine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe resulting solution was warmed
  2. 2
    Temperaturto reflux for 16 h
  3. 3
    Waschenwashed with water (2×100 mL)
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Einengenwas concentrated in vacuo
  7. 7
    SonstigePurification by flash chromatography (EtOAc)

Vorschrift

A solution of 3,5-dibromopyridine (2.5 g, 10.5 mmol), PPh3 (210 mg, 0.8 mmol) in degassed THF (2 mL) was treated with Pd2(dba)3 (Tris(dibenzylideneacetone)dipalladium (0), 91.5 mg, 0.1 mmol) at 25° C. under N2. A solution of 2-pyridinyl zinc chloride (21 mL, 0.5 M in THF, Aldrich) in THF was added and the resulting solution was warmed to reflux for 16 h. The solution was allowed to cool to room temperature, diluted with EtOAc (200 mL), washed with water (2×100 mL), dried (MgSO4), filtered and was concentrated in vacuo. Purification by flash chromatography (EtOAc) afforded the title compound as a white solid. MS 236 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06713455B2uspto-grants-2004_03