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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255158생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/255158

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물tert-butyl {1-[2-(7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl]piperidin-4-yl}carbamateHCID 59371209—
용매1,4-DioxaneHCID 31275—
생성물1-[2-(4-aminopiperidin-1-yl)ethyl]-7-methoxyquinolin-2(1H)-oneHCID 59398289101.3%

반응 단계

A solution of tert-butyl {1-[2-(7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl]piperidin-4-yl}carbamate (Intermediate 2, 150 mg, 0.37 mmol) in dioxane (4 mL) was treated at room temperature under vigorous stirring with a solution of HCl in dioxane (4M, 2 mL). After 18 hours, the reaction mixture was concentrated under reduced pressure. The residue was taken up in dichloromethane (60 mL) and saturated aqueous sodium hydrogen carbonate solution (10 mL). The aqueous phase was extracted three times with dichloromethane (3×50 mL) and the combined organic phases were dried over sodium sulfate and concentrated under reduced pressure to give 113 mg (100% yield) of the crude product as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875715B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-13619cdffa4f4909bd9fe5fb84e522fc
출처 메모uspto-grants-2011_01