HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → Paroxetine Impurity 10
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Paroxetine | HCID 43815 | — |
| Reactant | Phenylcarbamate | HCID 21896570 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Paroxetine Impurity 10 | HCID 206527 | — |
Reaction Steps
A round bottom flask was charged with unpurified paroxetine base (8.6 g) in toluene (20 ml) which had been prepared by potassium hydroxide hydrolysis of a phenylcarbamate derivative, and a solution of methanesulfonic acid (1.9 ml) in toluene (10 ml) was added dropwise. The resulting clear solution was placed into a separating funnel and extracted with water (30 ml). The aqueous phase was separated, residual toluene removed by evaporation at reduced pressure and the remaining clear solution (25 ml) was further diluted with water (40 ml). The water was removed by freeze drying to afford amorphous paroxetine methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063927 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-160d9eac20f045059b09b3fa6bc51c01 |
| Source note | uspto-grants-2000_05 |