反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[I:20]I.N1C=CN=C1.[CH2:27]([O:34][C:35](=[O:48])[CH2:36][C@H:37]([NH:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[CH2:38]O)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>C(Cl)Cl>[CH2:27]([O:34][C:35](=[O:48])[CH2:36][C@H:37]([NH:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[CH2:38][I:20])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1参加物
実験手順
A suspension of polymer bound triphenyl phosphine (18.25 g, 54.76 mmol) in DCM (100 ml) is treated with iodine (12.2 g, 48.1 mmol) and the reaction mixture stirred at ambient temperature for 15 minutes. Imidazole (3.72 g, 54.7 mmol) is added and the reaction mixture stirred for a further 15 minutes. A solution of (S)-3-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (6.76 g, 21.9 mmol) in DCM (100 ml) is added. The suspension is stirred at reflux for 1.5 hours, then filtered through Celite™ filter material, washing through with DCM. The combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine, then dried over magnesium sulphate and evaporated. The crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent to afford (S)-3-tert-butoxycarbonylamino-4-iodo-butyric acid benzyl ester. [M-BOC] 320.12
後処理
- additionA suspension of polymer
- stirringthe reaction mixture stirred for a further 15 minutes
- stirringThe suspension is stirred
- temperatureat reflux for 1.5 hours
- filtrationfiltered through Celite™
- filtrationfilter material
- washwashing through with DCM
- washThe combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine
- dry with materialdried over magnesium sulphate
- customevaporated
- customThe crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent
出典と根拠
- ORDレコード
- ord-03e7a4abcdd845eca11b0eb3e0bc38af
- 出典データセット
- uspto-grants-2007_10
- 特許番号
- US07288537B2
関連ノート
読み込み中…