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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212509생성일: 2026년 10월 27일

Potassium Carbonate → 6-[5-(Allyl-methyl-amino)-pentyloxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2212509

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물N-MethylallylamineHCID 69391—
반응물6-(5-Bromo-pentyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 69514902—
용매DimethylformamideHCID 6228—
생성물6-[5-(Allyl-methyl-amino)-pentyloxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl esterHCID 6951469972.1%

반응 단계

1.5 g (3.75 mmol) 6-(5-Bromo-pentyloxy)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester were treated with 355 mg (5 mmol) N-allyl-methylamine and 830 mg (6 mmol) K2CO3 (powdered) in 8 ml DMF at 60° C. for 3 h. The mixture was concentrated in vacuo, dissolved in acetone and filtered. The filtrate was concentrated and purified by column chromatography on silica gel with CH2Cl2/MeOH 19:1 to yield 1.05 g (72%) 6-[5-(Allyl-methyl-amino)-pentyloxy]-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester as colorless oil, MS: 389 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07102007B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-048023a5ba6746849aded0b059018011
출처 메모uspto-grants-2006_09