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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 656883생성일: 2026년 10월 25일

Toluene → 1-[2-(4-aminopiperidin-1-yl)ethyl]-7-methoxyquinolin-2(1H)-one

https://huagongshe.com/reaction/656883

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물tert-butyl {1-[2-(7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl]piperidin-4-yl}carbamateHCID 59371209—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물1-[2-(4-aminopiperidin-1-yl)ethyl]-7-methoxyquinolin-2(1H)-oneHCID 5939828954%

반응 단계

1,1-Dimethylethyl (1-{2-[7-(methyloxy)-2-oxo-1(2H)-quinolinyl]ethyl}-4-piperidinyl)carbamate (2.25 g; 5.61 mmol) was dissolved in a mixture of chloroform (20 ml) and HCl (15 ml) and stirred at rt under argon for 1 hour. The salts were dissolved in MeOH and a small amount of toluene added, all the solvents were then removed. The residues were redissolved in MeOH and stirred with amberlyst ion exchange resin until a neutral pH was reached. The resin was filtered off and the solvent removed and the crude residues were purified by column chromatography on silica gel using a 0-20% 2M NH3:MeOH/DCM gradient, to give the desired product (900 mg; 54%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071592B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-38651200edb34560991f3e690c603ce7
출처 메모uspto-grants-2011_12