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HRID 396172作成日:2026年10月25日

1,4-Dioxane → 1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthalene

https://huagongshe.com/reaction/396172

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物4-Bromo-1-naphthylamineHCID 75303—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
生成物1-Amino-4-[3-(morpholin-4-yl)phenyl]naphthaleneHCID 1208527538%

反応条件

温度100 °C

反応手順

The above intermediate (1.49 g, 3.51 mmol) and 1-amino-4-bromonaphthalene (0.69 g, 3.11 mmol) were dissolved in 20 mL anhydrous 1,4-dioxane in a sealable tube under inert gas atmosphere. The solution was degased and purged with nitrogen (2×). Tetrakis(triphenylphosphine)palladium(O) (0.21 g, 0.18 mmol) was added and the solution was degassed and purged with nitrogen again (2×). The tube was sealed and heated to 100° C. for 17 h. After cooling to room temperature the mixture was diluted with EtOAc, saturated aqueous potassium carbonate solution (10 mL) was added and the mixture was stirred for 1 h at room temperature. The mixture was filtered over diatomaceous earth and the layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered and evaporated to dryness. Purification of the residue by flash chromatography afforded 0.363 g (1.19 mmol, 38%) of title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608052B2
出典データセットuspto-grants-2003_08
ORD IDord-54b2d1b0418a48038e25e9b95d769945
出典メモuspto-grants-2003_08