Reaktion #11569

Reaktionsgleichung

Hydrochloric acid

1-[2-(1-adamantyl)ethyl]-1-benzyloxy-3-[3-(4-pyridyl)propyl]urea

→

titled compound

Ausbeute 34.0%

1-[2-(1-Adamantyl)ethyl]-1-hydroxy-3-[3-(4-pyridyl)propyl]urea

Ausbeute 34.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstige1-28) (438 mg, 0.978 mmol) in methanol (9.78 ml), and a nitrogen gas was bubbled through the mixture
2. 2
   workup.ADDITIONTo the mixture was added 10% palladium on carbon (43 mg)
3. 3
   FiltrationThe palladium on carbon was filtered out
4. 4
   Einengenthe filtrate was concentrated under reduced pressure
5. 5
   workup.ADDITIONthe concentrate was diluted with diethyl ether (30 ml)
6. 6
   WaschenThe whole was washed with a saturated aqueous sodium hydrogencarbonate solution (30 ml)
7. 7
   Trocknena saturated aqueous sodium chloride solution (30 ml) successively, and the organic layer was dried over magnesium sulfate
8. 8
   SonstigeThe solvent was evaporated under reduced pressure
9. 9
   Sonstigethe residue was purified by silica gel column chromatography

Vorschrift

2 N Hydrochloric acid (4.0 ml) was added to a solution of 1-[2-(1-adamantyl)ethyl]-1-benzyloxy-3-[3-(4-pyridyl)propyl]urea (Compound No. 1-28) (438 mg, 0.978 mmol) in methanol (9.78 ml), and a nitrogen gas was bubbled through the mixture. To the mixture was added 10% palladium on carbon (43 mg), and the whole was stirred under hydrogen at 1 atm for three days. The palladium on carbon was filtered out, the filtrate was concentrated under reduced pressure, and the concentrate was diluted with diethyl ether (30 ml). The whole was washed with a saturated aqueous sodium hydrogencarbonate solution (30 ml) and a saturated aqueous sodium chloride solution (30 ml) successively, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give 119 mg (34%) of the titled compound.

Quelle