HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 7,8,9,10-tetrahydro-3-methoxy-2-[3-(4-phenyl-1-piperazinyl)propoxy]-6H-dibenzo[b,d]pyran-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Fumarate | HCID 5460307 | — |
| Reactant | 7,8,9,10-tetrahydro-2-[3-(methanesulfonyloxy)propoxy]-3-methoxy-6H-dibenzo[b,d]pyran-6-one | HCID 19927709 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 7,8,9,10-tetrahydro-3-methoxy-2-[3-(4-phenyl-1-piperazinyl)propoxy]-6H-dibenzo[b,d]pyran-6-one | HCID 19927637 | 94% |
Reaction Steps
Method B (24 h at 60° C.); starting materials: 7,8,9,10-tetrahydro-2-[3-(methanesulfonyloxy)propoxy]-3-methoxy-6H-dibenzo[b,d]pyran-6-one (example 80) and 1-phenylpiperazine; yield 94%; fusion point 104°-106° C. (from TBME and isopropanol). Fumarate: method E; yield 92%; fusion point 160°-161° C. (from ethanol and acetone).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428038 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-06983b3b92bb4e458a75cae28a70b5ba |
| Source note | uspto-grants-1995_06 |