反応式
[F:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[C@:12]12[CH2:17][C@H:16]1[CH2:15][NH:14][CH2:13]2.Br[CH2:19][CH2:20][CH2:21][O:22][Si:23]([C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:25])[CH3:24].C(N(CC)CC)C.N[C@H](C(O)=O)CC1C=C2C(C=CC=C2)=CC=1>C1COCC1>[CH3:28][C:26]([Si:23]([CH3:25])([CH3:24])[O:22][CH2:21][CH2:20][CH2:19][N:14]1[CH2:15][C@H:16]2[C@:12]([C:3]3[CH:4]=[CH:5][C:6]([C:8]([F:11])([F:10])[F:9])=[CH:7][C:2]=3[F:1])([CH2:17]2)[CH2:13]1)([CH3:27])[CH3:29]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of (1S,5R)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane (150 mg, 0.6 mmol), [(3-bromopropyl)oxy](1,1-dimethylethyl)dimethylsilane (233 mg, 0.92 mmol), triethylamine (185 mg, 1.83 mmol) and Nal (20 mg) in THF (2 mL) was stirred at r.t. for 20 h. The reaction mixture was concentrated under vacuum, water was added and the aqueous phase was extracted with EtOAc. The organic phase was dried over Na2SO4 and filtered. The filtrate was concentrated under vacuum and the crude was purified by column chromatography (eluting with EtOAc/cyclohexane 3/7) to give 245 mg of the title compound.
後処理
- concentrationThe reaction mixture was concentrated under vacuum, water
- additionwas added
- extractionthe aqueous phase was extracted with EtOAc
- dry with materialThe organic phase was dried over Na2SO4
- filtrationfiltered
- concentrationThe filtrate was concentrated under vacuum
- customthe crude was purified by column chromatography (eluting with EtOAc/cyclohexane 3/7)
出典と根拠
- ORDレコード
- ord-d661de3d79454f38b7d20a768ef01a40
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07875643B2
関連ノート
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