Réaction #77253

ord-19a20f7f68d44d88ab8d02b254a6f989

Équation de réaction

Cc1cccnc1C(=O)c1ccc(F)c(N)c1
3-amino-4-fluorophenyl 3-methyl-2-pyridyl ketone
N#C[S-].[Na+]
sodium thiocyanate
CC(=O)O
acetic acid
BrBr
bromine
CC(=O)O
acetic acid
Cc1cccnc1C(=O)c1cc(N)c(F)cc1SC#N
title compound
Rendement 100.0%
Cc1cccnc1C(=O)c1cc(N)c(F)cc1SC#N
4-Amino-5-fluoro-2-(3-methylpicolinoyl)phenyl thiocyanate
Rendement 100.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe precipitate is filtered
  2. 2
    Autredried

Mode opératoire

To a mixture of 3-amino-4-fluorophenyl 3-methyl-2-pyridyl ketone(4.20 g, 0.171 mol), sodium thiocyanate (4.19 g, 0.0517 mol) and glacial acetic acid is added a solution of bromine in acetic acid (2M, 12 ml, 0.0240 mol) over a one hour period. The resultant mixture is stirred one hour at room temperature and poured into cold water. The precipitate is filtered and dried to afford the title compound as a green solid (5.43 g, >100%) which is identified by NMR and mass spectral analysis.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06706663B2uspto-grants-2004_03