Dicyclohexylcarbodiimide → Boc-Asp(OBzl)-NHMe
反応式
[NH:1]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[C@H:2]([C:14](O)=[O:15])[CH2:3][C:4](=[O:13])[O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH:24]1([N:30]=C=NC2CCCCC2)CCCCC1.OC1C2N=NNC=2C=CC=1.Cl.CN.C(N(C(C)C)CC)(C)C>O1CCCC1>[NH:1]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[C@H:2]([C:14]([NH:30][CH3:24])=[O:15])[CH2:3][C:4](=[O:13])[O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1参加物
7
実験手順
Boc-Asp(OBzl) (6.4 g) was dissolved in tetrahydrofuran (30 ml), added with dicyclohexylcarbodiimide (4.1 g), hydroxybenzotriazole (3.0 g), methylamine hydrochloride (2.0 g) and diisopropylethylamine (3.9 g) under ice cooling and stirred for 10 hours. Insolubles were removed from the mixture by filtration and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the organic layer was washed with 10% aqueous solution of citric acid and saturated aqueous solution of sodium hydrogen carbonate and dried over anhydrous sodium sulfate. Then the ethyl acetate was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to give Boc-Asp(OBzl)-NHMe (3.9 g).
後処理
- customInsolubles were removed from the mixture by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- dissolutionThe residue was dissolved in ethyl acetate
- washthe organic layer was washed with 10% aqueous solution of citric acid and saturated aqueous solution of sodium hydrogen carbonate
- dry with materialdried over anhydrous sodium sulfate
- customThen the ethyl acetate was evaporated under reduced pressure
- customThe residue was recrystallized from ethyl acetate/hexane
出典と根拠
- ORDレコード
- ord-df6ae7d590dc4e59bae0eef0e6407b33
- 出典データセット
- uspto-grants-1998_06
- 特許番号
- US05763408
反応ノート
読み込み中…