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HRID 521406作成日:2026年10月26日

1,4-Dioxane → Methyl 4-methyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate

https://huagongshe.com/reaction/521406

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Cyclohexanecarboxylic acid, 2-oxo-, methyl esterHCID 170489—
反応物Methyl 3-amino-4-methylbenzoateHCID 337778—
溶媒WaterHCID 962—
生成物Methyl 4-methyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylateHCID 8966951331.7%

反応条件

温度130 °C

反応手順

A mixture of methyl 2-oxocyclohexanecarboxylate (1.0 g, 6.4 mmol), methyl 3-amino-4-methylbenzoate (1.06 g, 6.4 mmol), polyphosphoric acid (4 mL) and dioxane (6 mL) was heated at 130° C. for 2 hours. After cooling to room temperature, the mixture was diluted with water (100 mL) and the resulting precipitate was collected by filtration and dried. The solid was suspended in methanol (100 mL) and SOCl2 (10 mL) was added. The mixture was stirred at reflux for 5 hours, concentrated and treated with water (80 mL), extracted with ethyl acetate (3×80 mL). The organic layer was separated, concentrated to give the crude product. Then the mixture was purified by chromatography column on silica gel (eluted with CH2Cl2/MeOH) to afford crude product, and the final product (0.55 g) was obtained from recrystallization using MeOH as solvent. 1H NMR (DMSO-d6) δ 10.3 (s, 1H), 7.41 (d, 1H, J=7.8 Hz), 6.99 (d, 1H, J=7.8 Hz), 3.73 (s, 3H), 2.78-2.81 (m, 2H), 2.50 (s, 3H), 2.35-2.37 (m, 2H), and 1.64-1.73 (m, 4H). MS (ESI) m/e [M+1]+272.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328111B2
出典データセットuspto-grants-2016_05
ORD IDord-40aa67c6e29f42c98fda582dab79a74b
出典メモuspto-grants-2016_05