Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62236생성일: 2026년 10월 25일
p-Toluenesulfonic acid → (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/62236
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 1-Benzylpiperidine-4-carbaldehyde | HCID 89584 | — |
| 반응물 | 6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one | HCID 117940128 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one | HCID 117940242 | — |
반응 단계
To a solution of 13 (150 mg, 0.607 mmol) in toluene 15 mL was added 1-benzylpiperidine-4-carbaldehyde 21 (123.4 mg, 0.607 mmol). p-Toluene sulphonic acid (PTSA) (230.9 mg, 1.214 mmol) was added to the reaction mixture, and stirred at 120° C. for 6 h. The reaction mass was diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude material, which was purified through flash chromatography using 100-200 mesh silica gel. Eluting at 30% ethyl acetate in hexane gave yellow coloured solid (E)-2-((1-benzylpiperidin-4-yl)methylene)-6-methoxy-5-morpholino-2, 3-dihydro-1H-inden-1-one 22.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09446047B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-5de892651a514d5ca22c4e338408d1f5 |
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| 출처 메모 | uspto-grants-2016_09 |
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