反応式
C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.N1C=CN=C1.[I:25]I.[CH2:27]([O:34][C:35]1[CH:40]=[C:39]([CH2:41]O)[CH:38]=[CH:37][C:36]=1[N:43]1[S:47](=[O:49])(=[O:48])[N:46]([CH2:50][CH2:51][Si:52]([CH3:55])([CH3:54])[CH3:53])[C:45](=[O:56])[CH2:44]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>C(Cl)Cl>[CH2:27]([O:34][C:35]1[CH:40]=[C:39]([CH2:41][I:25])[CH:38]=[CH:37][C:36]=1[N:43]1[S:47](=[O:49])(=[O:48])[N:46]([CH2:50][CH2:51][Si:52]([CH3:55])([CH3:54])[CH3:53])[C:45](=[O:56])[CH2:44]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 0 °C
実験手順
To a 0° C. slurry of resin-bound PPh3 (850 mg, 2.5 mmol) in CH2Cl2 (10 mL) in a pressure vessel is added imidazole (200 mg, 2.8 mmol) and iodine (650 mg, 2.5 mmol). The mixture is vigorously stirred at 0° C. for 30 min. To the mixture is added a solution of 5-(2-benzyloxy-4-hydroxymethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (550 mg, 1.2 mmol) in CH2Cl2 (10 mL) dropwise. The vessel is sealed and heated to 45° C., with stirring, for 2 h. The reaction is allowed to cool to RT and the mixture is filtered through a plug of cotton to remove the resin. The organic solution is washed with sat. Na2SO3 and brine, then dried over MgSO4. The solvent is removed under reduced pressure to afford the title compound as a white solid which is used in the next step without further purification: (M+H)+=576.
後処理
- customThe vessel is sealed
- temperatureheated to 45° C.
- stirringwith stirring, for 2 h
- temperatureto cool to RT
- filtrationthe mixture is filtered through a plug of cotton
- customto remove the resin
- washThe organic solution is washed with sat. Na2SO3 and brine
- dry with materialdried over MgSO4
- customThe solvent is removed under reduced pressure
出典と根拠
- ORDレコード
- ord-e414390b6c7b4237afa1d6e317f7f2ea
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08084448B2
関連ノート
読み込み中…