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HRID 75147作成日:2026年10月23日

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → 1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol

https://huagongshe.com/ja/reaction/75147

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2-[4-(Benzyloxy)phenyl]oxiraneHCID 13248717—
溶媒IsopropanolHCID 3776—
生成物1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanolHCID 5943717623.2%

反応手順

2-(4-(benzyloxy)phenyl)oxirane (2 g, 8.8 mmol) and (1-adamantylmethyl)amine (1.46 g, 8.8 mol) were dissolved in isopropyl alcohol (30 mL) and heated under reflux overnight. The mixture was concentrated to give the crude product, which was purified by column chromatography to afford 1-(4-(benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol (0.8 g, 23%). 1H NMR: (CDCl3, 400 MHz) δ=1.51 (m, 6H), 1.60-1.72 (m, 6H), 1.97 (m, 3H), 2.32&2.45 (dd, 2H), 2.64 (m, 1H), 2.73 (m, 1H), 2.94 (m, 1H), 3.40 (brs, 3H), 4.79 (m, 1H), 6.93 (m, 2H), 7.26-7.43 (m, 7H).

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-88047b6c7522438b9fa11d82686d0f95
出典メモuspto-grants-2014_09