Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 611120생성일: 2026년 10월 27일
Dimethylamine → 2-(4-Benzyloxy-3-methoxy-phenyl)-1-(2-dimethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)ethane-1-one
https://huagongshe.com/reaction/611120
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylamine | HCID 674 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | 2-(4-benzyloxy-3-methoxyphenyl)-1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)ethan-1-one | HCID 19600197 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 2-(4-Benzyloxy-3-methoxy-phenyl)-1-(2-dimethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)ethane-1-one | HCID 19599997 | — |
반응 단계
To a solution of 0.290 g (0.768 mmol) of 2-(4-benzyloxy-3-methoxyphenyl)-1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)ethan-1-one in 20 ml of acetic acid, 0.104 ml (1.15 mmol) of 50% aqueous dimethylamine and 0.094 ml (1.15 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 40 minutes. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with 5% aqueous sodium hydrogen carbonate and extracted with dichloromethane 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform to chloroform/methanol=50/1 to 25/1) to yield the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05998433 |
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| 출처 데이터셋 | uspto-grants-1999_12 |
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| ORD ID | ord-4661598492f64e5ab33222ac992808a7 |
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| 출처 메모 | uspto-grants-1999_12 |
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