HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-(8-Aza-bicyclo[3.2.1]oct-8-yl)-4-[4-(2-methoxy-5-trifluoromethyl-phenyl)-piperazin-1-yl]-2-phenyl-butan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(2-Methoxy-5-trifluoromethyl-phenyl)-piperazine | HCID 15124794 | — |
| Reactant | 1-(8-Aza-bicyclo[3.2.1]oct-8-yl)-4-chloro-2-phenyl-butan-1-one | HCID 19968360 | — |
| Reactant | Hydrate;dihydrochloride | HCID 21226127 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(8-Aza-bicyclo[3.2.1]oct-8-yl)-4-[4-(2-methoxy-5-trifluoromethyl-phenyl)-piperazin-1-yl]-2-phenyl-butan-1-one | HCID 19968352 | 67.5% |
Reaction Steps
The title compound was prepared from 4-(2-methoxy-5-trifluoromethyl-phenyl)-piperazine 0.7 g, 2.3 mmole, prepared according to the method reported in example 2), 1-(8-aza-bicyclo[3.2.1]oct-8-yl)-4-chloro-2-phenyl-butan-1-one (0.7 g, 2.3 mmole), diisopropylethylamine (0.4 g, 3.0 mmole) and potassium iodide (0.5 g, 3.0 mmole) in dimethylformamide (25 mL) in the manner described in example 2 to yield 0.8 g of title product as the hydrochloride hemihydrate, m.p. 198°-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05610154 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-b935bc3b175849baa31fb096d79f71fc |
| Source note | uspto-grants-1997_03 |