Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1532055생성일: 2026년 10월 27일
Potassium Carbonate → (S)-N-(2,3-dihydrofuro[3,2-f]-1,4-benzodioxin-2-ylmethyl)-1-[1-(2-methoxyphenyl)piperid-4-yl]methylamine monofumarate monohydrate
https://huagongshe.com/reaction/1532055
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Fumaric Acid | HCID 444972 | — |
| 반응물 | (1-(2-Methoxyphenyl)piperidin-4-yl)methanamine | HCID 10608971 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (S)-N-(2,3-dihydrofuro[3,2-f]-1,4-benzodioxin-2-ylmethyl)-1-[1-(2-methoxyphenyl)piperid-4-yl]methylamine monofumarate monohydrate | HCID 22951199 | 187% |
반응 단계
A mixture of the product from the previous reaction (2.80 g), potassium carbonate (10.0 g) and 1-[(2-methoxyphenyl)piperid-4-yl]methylamine (1.88 g) in dry acetonitrile (100 ml) was heated under reflux with stirring for 90 hours. The cooled mixture was filtered and the filtrate evaporated under reduced pressure to leave a pale-yellow oil. Purification by flash column chromatography on silica eluting with a 19:1 mixture of dichloromethane and methanol gave a pale-yellow oil which was then dissolved in ethanol (5 ml) and treated with a solution of fumaric acid (0.70 g) in ethanol (5 ml). The solvent was evaporated from the resulting solution under reduced pressure to give (S)-N-(2,3-dihydrofuro[3,2-f]-1,4-benzodioxin-2-ylmethyl)-1-[1-(2-methoxyphenyl)piperid-4-yl]methylamine monofumarate monohydrate (3.06 g) as a pale-yellow solid m.p. 95-6° C., [α]D=−38.5° (C=0.301, MeOH)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06201004B1 |
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| 출처 데이터셋 | uspto-grants-2001_03 |
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| ORD ID | ord-110740fe11a748f09ae454e8cbe6540c |
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| 출처 메모 | uspto-grants-2001_03 |
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