1,1'-Thiocarbonyldi-2(1H)-pyridone → 4-Methoxycarbonyl-3-nitrophenyl isothiocyanate

Beteiligte Stoffe

Reaktionsschritte

A solution of the above synthesized methyl 4-amino-2-nitrobenzoate (50 mg, 0.25 mmol) and 1,1′-thiocarbonyldi-2(1H)-pyridone (59 mg, 0.25 mmol) in dichloromethane (4.2 ml) was stirred at room temperature for 3 hours. After completion of the reaction, the solvent was evaporated, followed by purification with a silica gel column chromatography to obtain 42 mg of the desired product as a colorless oil (yield 69%).

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