Potassium Carbonate → {2-[7-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl]ethyl}tert-butyl-carbamate
反応式
Cl.Cl.[CH2:3]([N:10]1[CH2:17][CH:16]2[O:18][CH:12]([CH2:13][NH:14][CH2:15]2)[CH2:11]1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:19]([NH:23][C:24](=[O:29])[O:25][CH2:26][CH2:27]Br)([CH3:22])([CH3:21])[CH3:20].C([O-])([O-])=O.[K+].[K+]>C(#N)C>[CH2:3]([N:10]1[CH2:17][CH:16]2[O:18][CH:12]([CH2:13][N:14]([CH2:27][CH2:26][O:25][C:24](=[O:29])[NH:23][C:19]([CH3:22])([CH3:21])[CH3:20])[CH2:15]2)[CH2:11]1)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 70 °C
実験手順
A mixture of 3-benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane dihydrochloride (8 g, 0.0275 mol, 1.0 eq.; see WO 01/28992), 2-bromoethyl tert-butylcarbamate (9.23 g, 0.0412 g, 1.5 eq.) and fused K2CO3 (18.96 g, 0.1375 mol, 5.0 eq.) in dry acetonitrile (120 mL) was stirred at 70° C. overnight under a N2 atmosphere. The reaction mixture was cooled to RT, filtered and concentrated under reduced pressure. The resulting resiude was purified by column chromatography over silica gel (using 92:8 DCM:methanol as final eluent) to yield the sub-title compound (5 g, 43%).
後処理
- temperatureThe reaction mixture was cooled to RT
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe resulting resiude was purified by column chromatography over silica gel (using 92:8 DCM:methanol as final eluent)
出典と根拠
- ORDレコード
- ord-872a0dc3244d4082970966248a8ba36c
- 出典データセット
- uspto-grants-2010_01
- 特許番号
- US07648985B2
反応ノート
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