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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39853생성일: 2026년 10월 24일

2,3-Dihydro-1,4-benzodioxin-6-methylamine → 1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)cyclohexyl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-one

https://huagongshe.com/ko/reaction/39853

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dihydro-1,4-benzodioxin-6-methylamineHCID 87102—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)-4-oxocyclohexanecarbonitrileHCID 67539628—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)cyclohexyl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-oneHCID 5939840744.7%

반응 조건

온도40 °C

반응 단계

To a mixture of 3 mL of ethanol and 3 mL of dichloromethane solution containing 0.18 g of 1-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)-4-oxocyclohexanecarbonitrile, 1 mL of ethanol solution containing 0.13 g of (2,3-dihydrobenzo[b][1,4-]dioxin-6-yl)methylamine, 0.30 g of molecular sieves 3A, and 45 μL of acetic acid were added at room temperature. After stirred at 40° C. for 1.5 hours, the mixture was cooled to the room temperature, 36 mg of sodium cyanoborohydride was added, and stirred at the same temperature for 15 min. To the reaction mixture, aqueous saturated sodium hydrogen carbonate solution and chloroform were added, the organic layer was separated, washed with aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by flash silica gel column chromatography [hexane:ethyl acetate=4:1], to give (A) 36 mg of 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-1-(2-(7-methoxy-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)ethyl)cyclohexanecarbonitrile as a colorless oil and (B) 0.11 g of 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-1-(2-(7-methoxy-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)ethyl)cyclohexanecarbonitrile as a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ad125c172a2441629fd8ab4adf51811e
출처 메모uspto-grants-2013_09