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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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Fumaric AcidHCID 444972—
반응물(1-(2-Methoxyphenyl)piperidin-4-yl)methanamineHCID 10608971—
용매EthanolHCID 702—
용매AcetonitrileHCID 6342—
생성물(S)-N-(2,3-dihydrofuro[3,2-f]-1,4-benzodioxin-2-ylmethyl)-1-[1-(2-methoxyphenyl)piperid-4-yl]methylamine monofumarate monohydrateHCID 22951199187%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06201004B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-110740fe11a748f09ae454e8cbe6540c
출처 메모uspto-grants-2001_03