Реакция #160215
ord-4ff4a8cf9f464d6d9c7229379c5ccfbb
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1workup.STIRRINGthe reaction mixture was stirred for 3 hours
- 2Фильтрацияfiltered
- 3Концентрированиеconcentrated in vacuo
- 4ДругоеThe residue was purified by silica gel column chromatography
- 5Другоеto give the ether intermediate as pale yellow oil
- 6ФильтрацияThe reaction mixture was filtered
- 7Концентрированиеconcentrated in vacuo
- 8workup.ADDITIONdiluted with ethyl acetate
- 9Промывкаwashed with 1:1 3M NaOH/
- 10Сушкаaq. NaHCO3, dried over MgSO4
- 11Фильтрацияfiltered
- 12Концентрированиеconcentrated in vacuo
Методика
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).