Réaction #76790

Équation de réaction

phenyl isocyanate

5′-aminospiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine]

→

title compound

Rendement 86.0%

5′-Phenylaminocarbonylaminospiro[1-azabicyclo [2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine]

Rendement 86.0%

Solvants

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   AutreThe solvent was evaporated under reduced pressure
2. 2
   Autrethe residue purified by flash chromatography through silica gel
3. 3
   Lavageeluting with ammoniated chloroform/methanol (92.5:7.5)

Mode opératoire

Under a nitrogen atmosphere, phenyl isocyanate (0.056 mL, 0.515 mmol) was added to a suspension of 5′-aminospiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine] (119 mg, 0.514 mmol) in anhydrous tetrahydrofuran (5 mL) and stirred for 12 hours. The solvent was evaporated under reduced pressure and the residue purified by flash chromatography through silica gel, eluting with ammoniated chloroform/methanol (92.5:7.5), to obtain the title compound (155 mg, 0.442 mmol, 86%) as an off-white solid: electrospray MS (m/z, relative intensity) 351 ([MH]+, 100).

Source