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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1532055Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktFumaric AcidHCID 444972—
Edukt(1-(2-Methoxyphenyl)piperidin-4-yl)methanamineHCID 10608971—
LösungsmittelEthanolHCID 702—
LösungsmittelAcetonitrileHCID 6342—
Produkt(S)-N-(2,3-dihydrofuro[3,2-f]-1,4-benzodioxin-2-ylmethyl)-1-[1-(2-methoxyphenyl)piperid-4-yl]methylamine monofumarate monohydrateHCID 22951199187%

Reaktionsschritte

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)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06201004B1
Quelldatensatzuspto-grants-2001_03
ORD IDord-110740fe11a748f09ae454e8cbe6540c
Quellennotizuspto-grants-2001_03