2-Cyanoethyl tetraisopropylphosphorodiamidite → N-biotinyl-aminoethyl 2-cyanoethyl N,N-diisopropylphosphoramidite

HRID 1165363

反応式

HRID 1165363 の反応式
[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

6

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

  1. extractionThe mixture was extracted with two 50 ml portions of methylene chloride
  2. washthe combined extracts were washed with 5% sodium bicarbonate and brine
  3. dry with materialdried over sodium sulfate
  4. 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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