HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 68855422, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 68852018 | HCID 68852018 | — |
| Reactant | HCID 68852039 | HCID 68852039 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68855422 | HCID 68855422 | — |
Reaction Steps
In an analogous manner to Example 135, step 4 1-[1-(2′-fluoro-1,1′-biphenyl-3-yl)-2-piperazin-1-ylethyl]cyclohexanol dihydrochloride was prepared from tert-butyl 4-[2-(2′-fluoro-biphenyl-3-yl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate. The compound was neutralized with 10% aqueous potassium carbonate, and the residue dissolved in methanol. One equivalent of maleic acid was then added and the solution was concentrated. The product was triturated with diethyl ether to yield 1-[1-(2′-fluoro-1,1′-biphenyl-3-yl)-2-piperazin-1-ylethyl]cyclohexanol maleate as a colorless solid. MS (ESI) m/z 383 ([M+H]+); Anal. Calcd for C24H31FN2O.C4H4O4.0.50H2O: C, 66.25; H, 7.15; N, 5.52. Found: C, 66.03; H, 7.38; N, 5.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07550456B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-35c8b74fb6214aaea507cbcc11fb692b |
| Source note | uspto-grants-2009_06 |