Réaction #531820

ord-07a0a5f9562d4b0e805cc4892c81141b

Équation de réaction

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

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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 39.75 g of the title product as a white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08475819B2uspto-grants-2013_07