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HRID 1467550作成日:2026年10月25日

Methanol → Methyl 2-(4-(diethoxymethyl)phenyl)-3-(4-(4-isobutyrylpiperazine-1-carbonyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate

https://huagongshe.com/reaction/1467550

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium MethoxideHCID 10942334—
反応物4-(4-Isobutyrylpiperazine-1-carbonyl)benzaldehydeHCID 86639031—
反応物HCID 178470922HCID 178470922—
溶媒Ethyl PropionateHCID 7749—
生成物Methyl 2-(4-(diethoxymethyl)phenyl)-3-(4-(4-isobutyrylpiperazine-1-carbonyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylateHCID 6726174225%

反応条件

温度0 °C

反応手順

A mixture of 4-(4-isobutyrylpiperazine-1-carbonyl)benzaldehyde (950 mg, 3.3 mmol) and (E)-4-(4-(diethoxymethyl)benzylideneamino)isobenzofuran-1(3H)-one (1.018 g, 3 mmol) in ethyl propionate (40 mL) was cooled to 0° C. Then a solution of sodium methoxide in methanol [sodium (345 mg, 12 mmol) in methanol (8 mL)] was added dropwise. After the addition, the mixture was stirred at room temperature for 24 hr. The mixture was quenched with water (10 mL) and solvent was removed in vacuum. The residue was dissolved in water, and then extracted with ethyl acetate (100 mL×4). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and concentrated to give crude product. The crude product was purified by chromatography (silica gel, petroleum ether/ethyl acetate=10:1 to 1:10) to give methyl 2-(4-(diethoxymethyl)phenyl)-3-(4-(4-isobutyrylpiperazine-1-carbonyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate (491 mg, yield 25%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08999987B2
出典データセットuspto-grants-2015_04
ORD IDord-209c528b78d944999490ebc666590c75
出典メモuspto-grants-2015_04