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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39849생성일: 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/39849

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dihydro-1,4-benzodioxin-6-methylamineHCID 87102—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물7-methoxy-4-methyl-1-(2-(4-oxocyclohexyl)ethyl)quinolin-2(1H)-oneHCID 59397850—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)cyclohexyl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-oneHCID 5939840728.9%

반응 단계

To 2 mL of methanol solution containing 45 mg of 7-methoxy-4-methyl-1-(2-(4-oxocyclohexyl)ethyl)quinolin-2(1H)-one and 21 mg of (2,3-dihydrobenzo[b][1,4-]dioxin-6-yl)methylamine, 10 μL of acetic acid and 12 mg of sodium cyanoborohydride were added, and stirred at the same temperature for 30 min. To the reaction mixture, water, chloroform and aqueous saturated sodium hydrogen carbonate solution 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 [eluent; chloroform:methanol=20:1], to give (A) 5.4 mg of 1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)cyclohexyl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-one as a yellow oil and (B) 17 mg of 1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)cyclohexyl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-one as a pale yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-fb4909861e6d428680e97b65ea149a99
출처 메모uspto-grants-2013_09