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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6680생성일: 2026년 10월 25일

Dimethyl acetylenedicarboxylate → 2-Methoxycarbonyl-6-chloro-7-methyl-4-oxoquinoline

https://huagongshe.com/reaction/6680

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl acetylenedicarboxylateHCID 12980—
반응물4-Chloro-3-methylanilineHCID 23536—
용매MethanolHCID 887—
생성물2-Methoxycarbonyl-6-chloro-7-methyl-4-oxoquinolineHCID 6843634681.7%

반응 단계

Alternatively, to a solution of 4-chloro-3-methyl aniline (20.0 g, 0.141 mol) in MeOH (400 mL) was added drop-wise dimethyl acetylenedicarboxylate (21.07 g, 0.148 mol). The reaction mixture was stirred at ambient temperature for 30 minutes. The solvent was removed by evaporation and the residue was added to stirred diphenyl ether (300 mL), which has been preheated to 250° C. After 30 minutes, the mixture was cooled to ambient temperature and the resulting precipitate was collected and washed with 1 L of hot petroleum ether to give a mixture (29.0 g) of 2-methoxycarbonyl-6-chloro-7-methyl-4-oxoquinoline and 2-methoxycarbonyl-6-chloro-5-methyl-4-oxoquinoline as a gray solid. The mixture was dissolved in boiling methanol (1 L) and filtered hot. The collected solids were boiled in 1.2 L of methanol and filtered hot to afford (6.45 g, 16%) of 2-methoxycarbonyl-6-chloro-7-methyl-4-oxoquinoline: 1H NMR (DMSO-d6) 2.41 (s, 3), 3.92 (s, 3), 6.58 (s, 1), 7.86 (s, 1), 7.96 (s, 1) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084142B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b1946fdbc0c24122be9c85cffe1099fa
출처 메모uspto-grants-2006_08