反応式
[C:1]([NH:16][CH:17](O)[CH3:18])(=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][C@H:6]1[C@@H:14]2[C@@H:9]([NH:10][C:11]([NH:13]2)=[O:12])[CH2:8][S:7]1.N1[C-]=NN=N1.C([NH2+]C(C)C)(C)C.[CH:32]([N:35]([CH:49]([CH3:51])[CH3:50])[P:36](N(C(C)C)C(C)C)[O:37][CH2:38][CH2:39][C:40]#[N:41])([CH3:34])[CH3:33].C(=O)(O)[O-:53].[Na+]>CN(C=O)C>[CH:32]([N:35]([CH:49]([CH3:51])[CH3:50])[P:36]([O:37][CH2:38][CH2:39][C:40]#[N:41])[O:53][CH2:18][CH2:17][NH:16][C:1](=[O:15])[CH2:2][CH2:3][CH2:4][CH2:5][C@H:6]1[C@@H:14]2[C@@H:9]([NH:10][C:11]([NH:13]2)=[O:12])[CH2:8][S:7]1)([CH3:34])[CH3:33]参加物
実験手順
To a solution of 150 mg of N-biotinylaminoethanol (2a) in 5 ml of dry DMF was added 65 mg of diisopropylammonium tetrazolide and 0.300 ml of 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite. The resulting solution was stirred at room temperature for 1.25 hr and then poured onto 50 ml of 5% aqueous sodium bicarbonate. The mixture was extracted with two 50 ml portions of methylene chloride, and the combined extracts were washed with 5% sodium bicarbonate and brine, dried over sodium sulfate, and evaporated to afford the crude product as a thick oil. This was dissolved in 2 ml of dry methylene chloride, affording a solution that was added dropwise to 30 ml of rapidly stirring petroleum ether. The colorless precipitate that formed was collected by suction filtration under argon, affording after drying at room temperature under vacuum 109 mg (43%) of a colorless solid.
後処理
- extractionThe mixture was extracted with two 50 ml portions of methylene chloride
- washthe combined extracts were washed with 5% sodium bicarbonate and brine
- dry with materialdried over sodium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-27e1cf4b3e724bb69da2d6e18c0549f7
- 出典データセット
- uspto-grants-1990_03
- 特許番号
- US04908453
関連ノート
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