Water → Tri-Boc Lysine-beta-aminoethyl Ester
反応式
[C:1]([N:8]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[C@H:9]([C:15]([OH:17])=[O:16])[CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:25](C(CN)O)([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26].[CH3:36][CH2:37][N:38]=C=NCCCN(C)C.Cl.O>ClCCl.CN(C)C1C=CN=CC=1>[NH2:38][CH2:37][CH2:36][O:16][C:15](=[O:17])[C@:9]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])([CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])[N:8]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[C:1]([O:3][C:4]([CH3:5])([CH3:7])[CH3:6])=[O:2]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Di-Boc lysine (770 grams, 2.2 mol) was dissolved in dichloromethane (4 liters). Bocethanolamine (340 grams, 2.1 mol) was added to the solution, along with 4-dimethylaminopyridine (50 grams.) EDC-HCl (450 grams, 2.35 mol) was added and the mixture was allowed to stir overnight at room temperature. Water (2 liters) was added and the mixture was stirred for 30 minutes. The layers were separated, and the aqueous layer was extracted with dichloromethane. The combined organics were washed with saturated sodium bicarbonate, 1N HCl solution, and brine. Solvent was removed under reduced pressure to give an oil. Mass recovery was 770 grams (68% yield).
後処理
- additionwas added
- stirringthe mixture was stirred for 30 minutes
- customThe layers were separated
- extractionthe aqueous layer was extracted with dichloromethane
- washThe combined organics were washed with saturated sodium bicarbonate, 1N HCl solution, and brine
- customSolvent was removed under reduced pressure
- customto give an oil
出典と根拠
- ORDレコード
- ord-02a25817089144c5a5880e63fe2b155b
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08552217B2
反応ノート
読み込み中…