Reacción #160215
ord-4ff4a8cf9f464d6d9c7229379c5ccfbb
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGthe reaction mixture was stirred for 3 hours
- 2Filtraciónfiltered
- 3Concentraciónconcentrated in vacuo
- 4OtroThe residue was purified by silica gel column chromatography
- 5Otroto give the ether intermediate as pale yellow oil
- 6FiltraciónThe reaction mixture was filtered
- 7Concentraciónconcentrated in vacuo
- 8workup.ADDITIONdiluted with ethyl acetate
- 9Lavadowashed with 1:1 3M NaOH/
- 10Secadoaq. NaHCO3, dried over MgSO4
- 11Filtraciónfiltered
- 12Concentraciónconcentrated in vacuo
Procedimiento
To [8-benzyl-10-(hydroxymethyl)-11-oxa-3,8-diazaspiro[5.5]undecan-3-yl]-(4-isopropoxy-3-methyl-phenyl)methanone hydrochloride salt (43 mg, 0.09 mmol) in DMF (0.5 mL) was added sodium hydride (11 mg, 0.30 mmol) and the reaction mixture was stirred for 20 minutes. Iodoethane (30 μL, 0.38 mmol) was added and the reaction mixture was stirred for 3 hours, then diluted with EtOAc, filtered, concentrated in vacuo. The residue was purified by silica gel column chromatography using 10-100 EtOAc/hexanes eluent to give the ether intermediate as pale yellow oil. The oil was dissolved in methanol (0.6 mL), and Pd (5 mg, 0.004 mmol) and ammonium formate (27 mg, 0.44 mmol) were added and the reaction mixture was heated at 75° C. for 40 minutes. The reaction mixture was filtered, concentrated in vacuo, diluted with ethyl acetate, washed with 1:1 3M NaOH/sat. aq. NaHCO3, dried over MgSO4, filtered and concentrated in vacuo to give [10-(ethoxymethyl)-11-oxa-3,8-diazaspiro[5.5]undecan-3-yl]-(4-isopropoxy-3-methyl-phenyl)methanone (25 mg, 74%) as a pale yellow oil. ESI-MS m/z calc. 390.5. Found 391.3 (M+1)+; Retention time: 1.17 minutes (3 min run).