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HRID 75154作成日:2026年10月24日

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide

https://huagongshe.com/ja/reaction/75154

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2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dioneHCID 59437173—
溶媒1,4-DioxaneHCID 31275—
生成物N-(1-adamantylmethyl)-5-methyl-3-oxohexanamideHCID 5943716254.4%

反応手順

A solution of 5-(3-methylbutanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (2.76 g, 12 mmol) and (1-adamantylmethyl)amine (2 g, 12 mmol) in anhydrous 1,4-dioxane (10 mL) was heated under reflux for 2 h. Solvent was removed in vacuo. The residue was diluted with EtOAc (50 mL), washed with water, aq K2CO3 and brine, dried over Na2SO4 and concentrated to dryness. The residue was purified by chromatography on a silica gel column eluted with 20:1 PE/EtOAc to give the N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide (1.90 g, 54.4%). 1H NMR: (400 MHz, CDCl3): δ=0.92 (s, 3H), 0.96 (s, 3H), 1.54 (s, 7H), 1.62-1.73 (m, 9H), 1.98 (s, 4H), 2.12(m, 1H), 2.45(d, 2H), 2.95(d, 2H), 3.65(s, 2H).

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-0ecc176c213940abade3d063b7446509
出典メモuspto-grants-2014_09