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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266160생성일: 2026년 10월 26일

2-Pyridinamine, N-methyl- → ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-[N-methyl-N-(2-pyridyl)aminomethyl]quinoline-3-carboxylate

https://huagongshe.com/reaction/266160

반응식

참여 물질

역할이름HCID투입량
반응물2-Pyridinamine, N-methyl-HCID 20727—
반응물Ethyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylateHCID 10813243—
용매2-MethoxyethanolHCID 8019—
생성물ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-[N-methyl-N-(2-pyridyl)aminomethyl]quinoline-3-carboxylateHCID 190323409%

반응 단계

A mixture of ethyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate (1.0 g), 2-(methylamino)pyridine (0.95 g) and 2-methoxyethanol (30 ml) was stirred under reflux for 17 hours. The reaction mixture was concentrated under reduced pressure. Water was added to the residue, and the resulting mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with hexane - ethyl acetate (3:2, v/v) gave ethyl 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-[N-methyl-N-(2-pyridyl)aminomethyl]quinoline-3-carboxylate (0.1 g, 9%). This compound was recrystallized from dichloromethane-ethanol. Pale yellow prisms, mp. 174°-175° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650410
출처 데이터셋uspto-grants-1997_07
ORD IDord-c6b16c641ff143efbe0a37014a7cb0db
출처 메모uspto-grants-1997_07