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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Fumaric Acid | HCID 444972 | — |
| Edukt | (1-(2-Methoxyphenyl)piperidin-4-yl)methanamine | HCID 10608971 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (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% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06201004B1 |
|---|
| Quelldatensatz | uspto-grants-2001_03 |
|---|
| ORD ID | ord-110740fe11a748f09ae454e8cbe6540c |
|---|
| Quellennotiz | uspto-grants-2001_03 |
|---|