戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 44651作成日:2026年10月25日

Morpholine → tert-butoxycarbonyl-(1S)-1-methyl-2-morpholin-4-yl-2-oxo-1-phenylethylamine

https://huagongshe.com/reaction/44651

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物DiisopropylethylamineHCID 81531—
反応物O-benzotriazol-1-yl-tetramethyluroniumHCID 130500—
反応物(S)-2-(Boc-amino)-2-phenylpropanoic acidHCID 13678038—
溶媒DimethylformamideHCID 6228—
生成物tert-butoxycarbonyl-(1S)-1-methyl-2-morpholin-4-yl-2-oxo-1-phenylethylamineHCID 5744416588%

反応手順

630 mg (2.374 mmol) of N-(tert-butoxycarbonyl)-2-phenyl-D-alanine were dissolved in 20 mL of dry DMF and O-(benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoborate (TBTU, 1.37 g, 4.27 mmol), morpholine (0.412 mL, 4.73 mmol) and diisopropylethylamine (1.63 mL, 9.5 mol) were added. The mixture was stirred at room temperature for 1 hour, then the solvent was removed and the residue dissolved with dichloromethane. The solution was washed with saturated NaHCO3, brine, water and dried over Na2SO4. 700 mg of the title compound were recovered (88% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541429B2
出典データセットuspto-grants-2013_09
ORD IDord-b8729780c0e546f6bf715a96e00cab8d
出典メモuspto-grants-2013_09