Reacción #797293

Ecuación de reacción

2-Hydroxy-3-amino-5-bromopyridine

Pyridine

4-(trifluoromethyl)benzoyl chloride

→

titled compound

Rendimiento 52.4%

N-(5-bromo-2-hydroxypyridin-3-yl)-4-(trifluoromethyl)benzamide

Rendimiento 52.4%

Disolventes

DCM

water

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGAfter continuing stirring at rt for 30 mins
2. 2
   Otroreaction mass
3. 3
   Extracciónextracted with DCM
4. 4
   OtroDCM removed on rotavapour
5. 5
   Otroto obtain the crude
6. 6
   OtroCrude was purified on column
7. 7
   workup.ADDITIONa gradient mixture of MeOH and DCM (2:98) as eluent

Procedimiento

4-(Trifluoromethyl)benzoic acid (2.45 g, 12.9 mmol) dissolved in DCM (30 ml), cooled to 0° C. and added oxalyl chloride (3.4 ml, 38.6 mmol). Catalytic amount of DMF was added to this mixture and stirred at rt for 30 mins. After 30 mins, DCM removed on rotavapour and co-distilled the residue two times with DCM to obtain 4-(trifluoromethyl)benzoyl chloride quantitatively. 2-Hydroxy-3-amino-5-bromopyridine (2.4 g, 11.1 mmol) dissolved in DCM (15 ml) and added Pyridine (1.74 g, 22 mmol) under nitrogen atmosphere. This mixture stirred at rt for 30 mins and added 4-(trifluoromethyl)benzoyl chloride (2.4 g, 13.3 mmol). After continuing stirring at rt for 30 mins, reaction mass diluted with water and extracted with DCM. DCM removed on rotavapour to obtain the crude. Crude was purified on column using 60-120 mesh silica gel and a gradient mixture of MeOH and DCM (2:98) as eluent to afford the titled compound (2.1 g) as a brown solid. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): 12.43 (bs, 1H), 9.58 (s, 1H), 8.37 (d, J 2.6, 1H), 8.09 (d, J 8.2, 2H), 7.91 (d, J 8.2, 2H), 7.48 (d, J 2.6, 1H).

Fuente