HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Formaldehyde → 1,2,3,9-Tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Ondansetron | HCID 4595 | — |
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | 9-Methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one | HCID 598875 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 1,2,3,9-Tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one | HCID 11790505 | — |
Reaktionsschritte
Kim et al. (Heterocycles 1997, 45, 2041) disclose a two-step synthesis of ondansetron. In the first step of the synthesis, 1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one (compound of formula 1, Scheme 1) is reacted with a source of formaldehyde and morpholine in boiling glacial acetic acid to provide 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one (compound of formula 2, Scheme 1). In the second step of the synthesis, 1,2,3,9-tetrahydro-9-methyl-3-methylene-4H-carbazol-4-one is reacted with 2-methylimidazole in the presence of alumina (Al2O3) to provide ondansetron (See, Scheme 1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07696356B2 |
| Quelldatensatz | uspto-grants-2010_04 |
| ORD ID | ord-ab14a4ed59114cde9f6a7f164b3efe91 |
| Quellennotiz | uspto-grants-2010_04 |