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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-(Chloromethyl)-5-phenyl-1,3,4-oxadiazole | HCID 314941 | — |
| 반응물 | 6-Hydroxy-2-piperidinomethyltetralin | HCID 21939861 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochloride | HCID 22998553 | 69.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06310107B1 |
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| 출처 데이터셋 | uspto-grants-2001_10 |
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| ORD ID | ord-ce53b8eaa9ab4dfe8a27a4ed5c5660c3 |
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| 출처 메모 | uspto-grants-2001_10 |
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