Reaktion #5988
ord-299b2716a8194ac09bde2f6df2151eb9
Reaktionsgleichung
methyl chloroformate
1-methyl-5-(4-pyridinylamino)-1H-indole
→
solid
Ausbeute 98.4%
N-(1-Methyl-1H-indol-5-yl)-N-(4-pyridinyl) carbamic acid methyl ester
Ausbeute 98.4%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Waschenwas washed with water and saturated sodium chloride
- 2Trocknendried (anhydrous magnesium sulfate)
- 3Filtrationfiltered
- 4Sonstigeevaporated to 4 g of a solid
- 5WaschenElution through silica with 50% ethyl acetate in dichloromethane via flash column chromatography
Vorschrift
A solution of methyl chloroformate (1.3 g) in 5 ml DCM was added to a solution of 1-methyl-5-(4-pyridinylamino)-1H-indole (2.5 g) in 120 ml DCM and 6 ml triethylamine (4.4 g). After stirring one hour at ambient temperature the reaction mixture was washed with water and saturated sodium chloride, dried (anhydrous magnesium sulfate), filtered and evaporated to 4 g of a solid. Elution through silica with 50% ethyl acetate in dichloromethane via flash column chromatography yielded 3.1 g of a solid. Recrystallization from methanol yielded 2.4 g of crystals, mp 157°-159° C.