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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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물FormaldehydeHCID 712—
반응물2-(4-benzyloxy-3-methoxyphenyl)-1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)ethan-1-oneHCID 19600197—
용매Acetic AcidHCID 176—
생성물2-(4-Benzyloxy-3-methoxy-phenyl)-1-(2-dimethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)ethane-1-oneHCID 19599997—

반응 조건

온도100 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05998433
출처 데이터셋uspto-grants-1999_12
ORD IDord-4661598492f64e5ab33222ac992808a7
출처 메모uspto-grants-1999_12