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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943020생성일: 2026년 10월 27일

Acetic Acid → 1-methyl-3-({[2-phenyl-2-(tetrahydro-2H-pyran-4-yl)ethyl]amino}methyl)quinolin-2(1H)-one

https://huagongshe.com/reaction/1943020

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium AcetateHCID 517045—
반응물1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehydeHCID 4914628—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-phenyl-2-(tetrahydro-2H-pyran-4-yl)ethanaminium chlorideHCID 67393693—
용매1,2-DichloroethaneHCID 11—
생성물1-methyl-3-({[2-phenyl-2-(tetrahydro-2H-pyran-4-yl)ethyl]amino}methyl)quinolin-2(1H)-oneHCID 58415937—

반응 단계

1-methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehyde (35 mg, 0.187 mmol), sodium acetate (19.94 mg, 0.243 mmol), and 2-phenyl-2-(tetrahydro-2H-pyran-4-yl)ethanaminium chloride (45.2 mg, 0.187 mmol) were combined in 1,2 dichloroethane (2 ml). Acetic acid (0.021 ml, 0.374 mmol) and sodium triacetoxyborohydride (119 mg, 0.561 mmol) were added and the reaction stirred for 20 hours. The mixture was partitioned between CH2Cl2 and satd. bicarb and the aqueous portion was extracted 3×CH2Cl2. The organic portion was dried (Na2SO4) and concentrated in vacuo. The resulting material was purified by reversed-phase chromatography (10-60% ACN in water (with 2 ml/l NH4OH) over 20 min at 20 ml/min, 20×100 mm Phenomenex Gemini C18 column). Desired fractions were concentrated in vacuo. 50.5 mg, 73%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08389720B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-50dcf7ee4d7f482ebf7fc6e8c48bf8e5
출처 메모uspto-grants-2013_03