戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 75157作成日:2026年10月23日

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → HCID 59437175、化合物

https://huagongshe.com/ja/reaction/75157

反応式

関与物質

役割名称HCID仕込み量
反応物Tricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
反応物(S)-tert-butyl 2-(t-butyldimethylsilyloxymethyl)aziridine-1-carboxylateHCID 72525716—
溶媒DichloromethaneHCID 6344—
生成物HCID 59437175HCID 5943717542.5%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835426B2
出典データセットuspto-grants-2014_09
ORD IDord-b12f6b0d30474bdbb69a09795a73ce18
出典メモuspto-grants-2014_09