Reaktion #792162

ord-dd1922bf36334ab9a05313098f86dd08

Reaktionsgleichung

O=C([O-])[O-].[K+].[K+]
potassium carbonate
Clc1cccnc1Cl
2,3-dichloropyridine
Clc1cc[nH]n1
3-chloropyrazole
Clc1cc[nH]n1
product
Clc1cc[nH]n1
3-Chloropyrazole
Clc1ccn(-c2ncccc2Cl)n1
title product
Clc1ccn(-c2ncccc2Cl)n1
3-Chloro-2-(3-chloro-1H-pyrazol-1-yl)pyridine

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled to room temperature
  2. 2
    FiltrationThe precipitated solids were filtered
  3. 3
    Waschenwashed with water
  4. 4
    FiltrationThe solid filter cake
  5. 5
    Trocknendried over magnesium sulfate
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe crude solid was chromatographed on silica gel using 20% ethyl acetate/hexane as eluent

Vorschrift

To a mixture of 2,3-dichloropyridine (92.60 g, 0.629 mol) and 3-chloropyrazole (i.e. the product of Step B) (64.44 g, 0.629 mol) in N,N-dimethylformamide (400 mL) was added potassium carbonate (147.78 g, 1.06 mol), and the reaction mixture was then heated to 100° C. for 36 hours. The reaction mixture was cooled to room temperature and slowly poured into ice water. The precipitated solids were filtered and washed with water. The solid filter cake was taken up in ethyl acetate, dried over magnesium sulfate and concentrated. The crude solid was chromatographed on silica gel using 20% ethyl acetate/hexane as eluent to afford the title product as a white solid (39.75 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09173400B2uspto-grants-2015_11