Réaction #502095

ord-6444d2e501ee48d0b1e400257f4fc833

Équation de réaction

O
water
Nc1ccc(I)cn1
2-amino-5-iodopyridine
O=C(CBr)c1ccc(Cl)cc1
2-bromo-1-(4-chlorophenyl)ethanone
O=C([O-])O.[Na+]
sodium hydrogen carbonate
Clc1ccc(-c2cn3cc(I)ccc3n2)cc1
compound
Rendement 68.5%
Clc1ccc(-c2cn3cc(I)ccc3n2)cc1
2-(4-Chlorophenyl)-6-iodoimidazo[1,2-a]pyridine
Rendement 68.5%

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.WAITleft
  2. 2
    Températureto cool
  3. 3
    FiltrationThe precipitate is recovered by filtration
  4. 4
    Lavagewashed with water
  5. 5
    Autredried under reduced pressure

Mode opératoire

5.0 g of 2-amino-5-iodopyridine, 5.3 g of 2-bromo-1-(4-chlorophenyl)ethanone and 2.67 g of sodium hydrogen carbonate in 150 ml of n-propanol are placed in a round-bottomed flask. The mixture is heated at 80° C. for 40 h and left to cool, and 700 ml of water are added. The precipitate is recovered by filtration, washed with water and dried under reduced pressure. 5.51 g of compound are obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08088765B2uspto-grants-2012_01