Benzyl Bromide → N-Benzyl-N-{2-[7-(4-cyanobenzyl)-9-oxa-3,7-diazabicyclo[3.3.1]non-3-yl]-ethyl}methanesulfonamide
反応式
[H-].[Na+].[C:3]([C:5]1[CH:27]=[CH:26][C:8]([CH2:9][N:10]2[CH2:17][CH:16]3[O:18][CH:12]([CH2:13][N:14]([CH2:19][CH2:20][NH:21][S:22]([CH3:25])(=[O:24])=[O:23])[CH2:15]3)[CH2:11]2)=[CH:7][CH:6]=1)#[N:4].[CH2:28](Br)[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>CN(C=O)C>[CH2:28]([N:21]([CH2:20][CH2:19][N:14]1[CH2:15][CH:16]2[O:18][CH:12]([CH2:11][N:10]([CH2:9][C:8]3[CH:7]=[CH:6][C:5]([C:3]#[N:4])=[CH:27][CH:26]=3)[CH2:17]2)[CH2:13]1)[S:22]([CH3:25])(=[O:24])=[O:23])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a suspension of NaH (60% in oil, 0.039 g, 1.64 mmol) in dry DMF (10 mL) was added N-{2-[7-(4-cyanobenzyl)-9-oxa-3,7-diazabicyclo[3.3.1]-non-3-yl]ethyl}methanesulfonamide (0.3 g, 0.82 mmol; see Preparation M above) at 0° C. The reaction mixture was stirred for 1 h at room temperature. Benzyl bromide (0.155 g, 0.9 mmol) was added at 0° C. and the reaction mixture stirred at rt for 2 h. The reaction quenched with water, extracted with dichloromethane, washed with water, brine and then dried over sodium sulfate. Solvent evaporation under reduced pressure, followed by column chromatography of the residue over silica gel (using 5% methanol in chloroform as eluent) gave 160 mg of the title compound as a pale yellow solid.
後処理
- stirringthe reaction mixture stirred at rt for 2 h
- customThe reaction quenched with water
- extractionextracted with dichloromethane
- washwashed with water, brine
- dry with materialdried over sodium sulfate
- customSolvent evaporation under reduced pressure
出典と根拠
- ORDレコード
- ord-1cded3cc12a7447aba703097fd572790
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07354917B2
反応ノート
読み込み中…