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HRID 855891作成日:2026年10月24日

3-Amino-1-adamantanol → (2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrile

https://huagongshe.com/ja/reaction/855891

反応式

関与物質

役割名称HCID仕込み量
反応物3-Amino-1-adamantanolHCID 658645—
反応物(2S,5R)-1-(2-chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrileHCID 16090854—
溶媒AcetonitrileHCID 6342—
生成物(2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrileHCID 9973731—

反応手順

To a stirred solution of Example 8D (0.06 g, 0.305 mmol) in acetonitrile (3 mL) at room temperature under nitrogen, was added 3-amino-1-adamantanol (0.1 g, 0.61 mmol). The reaction mixture was stirred for two days and then concentrated under reduced pressure. The residue was flash chromatographed with 5-7% MeOH/CH2Cl2 to provide the desired compound as a pale yellow oil. MS (DCI) m/z 328 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 1.5-2 (14H, m), 2.11-2.21 (2H, m), 2.45-2.48 (2H, m), 3.78 (1H, d), 3.8-4.5 (2H, m), 4.53-4.55 (1H, t), 5.01 (1H, m), 5.05 (1H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07262207B2
出典データセットuspto-grants-2007_08
ORD IDord-2aee87f7866c4b93b3047e59f57ca720
出典メモuspto-grants-2007_08