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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132209생성일: 2026년 10월 25일

Potassium Carbonate → tert-Butyl 4-(3-oxo-3,4-dihydroisoquinolin-2(1H)-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/132209

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Amino-1-Boc-piperidineHCID 1268291—
반응물Methyl 2-[2-(chloromethyl)phenyl]acetateHCID 9855748—
용매AcetonitrileHCID 6342—
생성물tert-Butyl 4-(3-oxo-3,4-dihydroisoquinolin-2(1H)-yl)piperidine-1-carboxylateHCID 5973189740%

반응 단계

Potassium carbonate (1.4 g, 10 mmol) was added to a solution of methyl 2-(2-(chloromethyl)phenyl)acetate (940 mg, 4.7 mmol) in acetonitrile (20 mL). 4-Amino-N-Boc-piperidine (1.13 g, 5.6 mmol) was added to the mixture. Reaction was heated at reflux for 1 hour. Mixture was cooled to room temperature and then filtered over celite. Filtrate was concentrated in vacuo. Residue was treated with toluene (29 mL). Acetic acid (1.5 ml) was added to the mixture. Reaction was heated at reflux for 2 hours. Mixture was concentrated in vacuo. Residue was treated with ethyl acetate (50 mL). Mixture was washed successively with aqueous sodium bicarbonate (2×30 mL), 1N hydrochloric acid (30 mL), and brine (20 mL). Organic layer was dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography gave the title compound as lightly colored oil in 40% yield. MS m/e (M+H)+=331.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384930B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-7f3c353e3ba44efd995d03b8bbeced21
출처 메모uspto-grants-2008_06