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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469322생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/469322

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 14.0 mL (28.0 mmol) of a 2 M lithium diisopropylamide solution in 50 mL THF were cooled to −78° C. and combined with stirring with a solution of 5.00 g (25.1 mmol) of 2-chloro-6-methoxy-quinoline in THF. After 1 h stirring at −78° C., 4.5 mL (25.2 mmol) N-benzylpiperidone were added dropwise. After 1 h stirring at −78° C. the mixture was allowed to come up to RT and stirred overnight. The mixture was evaporated down i. vac. and purified by flash chromatography through Alox. The fractions containing the product were combined and evaporated down.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629137B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-86951bac4dce423987c5afaee4886243
출처 메모uspto-grants-2014_01