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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49478생성일: 2026년 10월 24일

N-Methylallylamine → 6-[4-(Allyl-methyl-amino)-butoxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/49478

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylallylamineHCID 69391—
반응물6-(4-Bromo-butoxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 69515181—
용매DimethylformamideHCID 6228—
생성물6-[4-(Allyl-methyl-amino)-butoxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 6951541774%

반응 단계

5.0 g (13.0 mmol) 6-(4-Bromo-butoxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester were treated with 3.66 g (51.5 mmol) N-allyl-methylamine in 100 ml DMF at 50° C. for 30 min. The mixture was concentrated in vacuo, dissolved in Et2O and water. The inorganic layer was extracted with Et2O, and the combined organic phases were washed with water and dried over Na2SO4. Purification by column chromatography on silica gel with CH2Cl2/MeOH 10:1 yielded 3.6 g (74%) 6-[4-(Allyl-methyl-amino)-butoxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester as light yellow oil, MS: 375 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706751B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-6b8b37ce99ad41bdb69ce4f9f30ee8ef
출처 메모uspto-grants-2004_03