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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74561생성일: 2026년 10월 26일

Tetrahydrofuran → 1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-ol

https://huagongshe.com/reaction/74561

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물2-Chloro-6-methoxyquinolineHCID 83647—
반응물Lithium diisopropylamideHCID 2724682—
반응물1-Benzyl-2-piperidoneHCID 5170076—
생성물1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-olHCID 58181126—

반응 조건

온도-78 °C

반응 단계

Under an argon atmosphere 5.0 g (25 mmol) 2-chloro-6-methoxyquinoline in a small amount of THF were added dropwise at −78° C. to 14 mL (28 mmol) of a 2 M lithium diisopropylamide solution (in THF) in 50 mL THF. Then the mixture was stirred for 1.5 h at −78° C. and 4.5 mL (25 mmol) N-benzylpiperidone was added dropwise. The mixture was stirred for a further 15 min with cooling before slowly being heated to RT. The reaction mixture was stirred overnight, evaporated down and purified by flash chromatography on aluminium oxide. The product-containing fractions were combined and evaporated down.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829006B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9443c894840b43aa8c4008ecd5502c39
출처 메모uspto-grants-2014_09