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3-Amino-1-adamantanol → (2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Amino-1-adamantanol | HCID 658645 | — |
| 反応物 | (2S,5R)-1-(2-chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrile | HCID 16090854 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07238724B2 |
| 出典データセット | uspto-grants-2007_07 |
| ORD ID | ord-bf71bd0cedcc4cde9110b3918333ac29 |
| 出典メモ | uspto-grants-2007_07 |