Reacción #2286282

Ecuación de reacción

[4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester

[4-(6-Chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester

sodium hydroxide

→

[4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid

[4-(6-Chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid

Disolventes

methanol

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroat room temperature
2. 2
   ConcentraciónAt this time, the reaction mixture was concentrated under vacuum
3. 3
   workup.ADDITIONThe resulting solid was diluted with water (200 mL)
4. 4
   Extracciónextracted with ethyl acetate (200 mL)
5. 5
   workup.ADDITIONThe water layer was acidified to pH=4 by the addition of a 1N aqueous hydrochloric acid solution
6. 6
   Extracciónwas extracted with ethyl acetate (2×200 mL)
7. 7
   Lavadowashed with a saturated aqueous sodium chloride solution
8. 8
   Secadodried with magnesium sulfate
9. 9
   Filtraciónfiltered
10. 10
    Concentraciónconcentrated under vacuum
11. 11
    Otroto afford a solid
12. 12
    OtroThe solid was dried overnight under high vacuum

Procedimiento

A solution of [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester (8a) (1.66 g, 4.75 mmol, contains a minor amount of isomer) in methanol (50 mL) at room temperature was treated dropwise with a 1N aqueous sodium hydroxide solution (9.5 mL, 9.50 mmol). The reaction was stirred at room temperature for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (200 mL) and extracted with ethyl acetate (200 mL). The ethyl acetate layer was discarded. The water layer was acidified to pH=4 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×200 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum to afford a solid. The solid was dried overnight under high vacuum to afford [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid (9a) (1.58 g, 100%, contains a minor amount of isomer) as an off-white solid; EI(+)-HRMS m/z calcd for C17H19ClN2O3 (M+) 334.1084, found 334.1083. Molecular Weight=334.8056; Exact Mass=334.1084

Fuente