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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 382981생성일: 2026년 10월 26일

Potassium Carbonate → 6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochloride

https://huagongshe.com/reaction/382981

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(Chloromethyl)-5-phenyl-1,3,4-oxadiazoleHCID 314941—
반응물6-Hydroxy-2-piperidinomethyltetralinHCID 21939861—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochlorideHCID 2299855369.2%

반응 단계

To a solution of 6-hydroxy-2-piperidinomethyltetralin (141 mg, free form of Reference Example 19) and 2-chloromethyl-5-phenyl-1,3,4-oxadiazole (148 mg) in DMF (3 ml) was added potassium carbonate (143 mg) and the reaction mixture was stirred at room temperature for 24 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried, and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate:methanol=10:1) and alumina column chromatography (eluent: ethyl acetate:hexane=1:4), and then converted into its hydrochloride, which was further recrystallized from methanol-diethyl ether to obtain the titled compound (175 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06310107B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-ce53b8eaa9ab4dfe8a27a4ed5c5660c3
출처 메모uspto-grants-2001_10