Reaktion #5576

Reaktionsgleichung

5-[2-(methylsulfonyloxy)etylthio]imidazo[1,2-a]pyridine

triethylamine

methylamine methanol

→

desired product

Ausbeute 47.1%

5-[2-(methylamino)ethylthio]imidazo[1,2-a]pyridine

Ausbeute 47.1%

Lösungsmittel

chloroform

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturat reflux for 3 hours
2. 2
   WaschenThe reaction mixture was washed with 3N NaOH
3. 3
   Trocknendried over anhydrous magnesium sulfate
4. 4
   workup.DISTILLATIONAfter the solvent was distilled off
5. 5
   Sonstigethe residue was purified by column chromatography [eluent: methanol/chloroform (1:10)]

Vorschrift

A solution of 5-[2-(methylsulfonyloxy)etylthio]imidazo[1,2-a]pyridine (2.18 g, 8 mmoles), triethylamine (2.24 ml, 16 mmoles) and a 40% methylamine-methanol solution (20 ml) in chloroform (20 ml) was heated at reflux for 3 hours. The reaction mixture was washed with 3N NaOH and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent: methanol/chloroform (1:10)] to obtain 781 mg of the desired product (47.1%, light brown oily product).

Quelle