関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tricyclo(3.3.1.13,7)dec-1-ylmethylamine | HCID 86625 | — |
| 反応物 | (S)-tert-butyl 2-(t-butyldimethylsilyloxymethyl)aziridine-1-carboxylate | HCID 72525716 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 59437175 | HCID 59437175 | 42.5% |
反応手順
To a solution of (1-adamantylmethyl)amine (15 g, 52 mmol) in anhydrous CH2Cl2 (50 mL) was added tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)aziridine-1-carboxylate (13 g, 78.3 mmol). The mixture was stirred for 10 min, the solvent was removed in vacuo and the residue was stirred at 40° C. for 5 h. The mixture was diluted with EtOAc (500 mL) and washed with water (100 mL),1N aq HCl (50 mL), satd aq NaHCO3 (50 ml) and brine (50 mL), and dried over MgSO4. The solution was concentrated to give a residue, which was purified by chromatography on silica gel to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-((1-adamantylmethyl)amino)propan-2-ylcarbamate (10 g, 24%). 1H NMR: (CDCl3, 400 MHz): δ=0.041 (s, 6H), 0.882 (s, 9H), 1.44 (s, 9H), 1.49 (s, 6H), 1.65 (m, 6H), 1.94 (s, 3H), 2.23 (s, 2H), 2.62-2.81 (m, 2H), 3.67 (m, 3H), 5.30 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835426B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-b12f6b0d30474bdbb69a09795a73ce18 |
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| 出典メモ | uspto-grants-2014_09 |
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