HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chloroform → 2,3-dihydro-7-methoxy-8-{3-[4-(2-methoxyphenyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Fumarate | HCID 5460307 | — |
| Edukt | N-(2-Methoxyphenyl)piperazine hydrochloride | HCID 9899402 | — |
| Edukt | 8-(3-chloropropoxy)-2,3-dihydro-7-methoxycyclopenta[c][1]benzopyran-4(1H)-one | HCID 19927690 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2,3-dihydro-7-methoxy-8-{3-[4-(2-methoxyphenyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-one | HCID 19927664 | 56% |
Reaktionsschritte
Method A (40 h at 50° C.); starting materials: 8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 83) and 1-(2-methoxyphenyl)piperazine hydrochloride; yield 56%; fusion point 177°-178° C. (from chloroform and ethanol). Fumarate: method E; yield 87%; fusion point 173°-174° C. (from acetone).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05428038 |
| Quelldatensatz | uspto-grants-1995_06 |
| ORD ID | ord-1427fd7ffd9d4cf99a055088fcb1a4b2 |
| Quellennotiz | uspto-grants-1995_06 |