反应详情

A round bottom flask was charged with 4-fluorophenylisothiocyanate (1 eq), 4-(3-Amino-4-methylamino-phenoxy)-pyridine-2-carboxylic acid tert-butyl ester (1 eq), and MeOH. The reaction was maintained stirring at room temperature overnight. Ferric chloride, (1.5 eq) was added and the resulting mixture was stirred overnight. The reaction was partitioned with EtOAc and water, and filtered through Celite. The layers were separated and the aqueous phase was neutralized with saturated Na2CO3 solution. The resulting aqueous phase was extracted with EtOAc and the mixture was filtered through Celite. The phases were separated and the aqueous phase was again extracted and filtered. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated to give a brown solid. The crude residue was purified by trituration in hot toluene to furnish the desired product. LCMS m/z 435.6 (MH+), tR=2.12 min.

1. temperatureThe reaction was maintained
2. stirringthe resulting mixture was stirred overnight
3. customThe reaction was partitioned with EtOAc and water
4. filtrationfiltered through Celite
5. customThe layers were separated
6. extractionThe resulting aqueous phase was extracted with EtOAc
7. filtrationthe mixture was filtered through Celite
8. customThe phases were separated
9. extractionthe aqueous phase was again extracted
10. filtrationfiltered
11. washThe combined organic layers were washed with brine
12. dry with materialdried over MgSO4
13. filtrationfiltered
14. concentrationconcentrated
15. customto give a brown solid
16. customThe crude residue was purified by trituration in hot toluene