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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 907811생성일: 2026년 10월 26일

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/907811

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참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium MethoxideHCID 10942334—
반응물4-(4-Isobutyrylpiperazine-1-carbonyl)benzaldehydeHCID 86639031—
반응물HCID 178470922HCID 178470922—
용매Ethyl PropionateHCID 7749—
생성물Methyl 2-(4-(diethoxymethyl)phenyl)-3-(4-(4-isobutyrylpiperazine-1-carbonyl)phenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylateHCID 6726174225%

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온도0 °C

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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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08012976B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-81ceb133959b4e55929017282de52009
출처 메모uspto-grants-2011_09