Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 86643031 | HCID 86643031 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Eprosartan Mesylate | HCID 5282474 | 89.8% |
Reaction Steps
Eprosartan acetate (30 gm, obtained in example 1) is suspended in acetone (450 ml) at 25-30° C., the suspension is cooled to 0-5° C., methanesulfonic acid (21.2 gm) is added drop wise while maintaining the temperature at 0-5° C. The temperature of the mass is raised to 25-30° C. and stirred for 5 hours. The mass is cooled to 0-5° C., stirred for 1 hour, the material is filtered and then suck dried. To the resulting wet cake is added acetone (60 ml) and stirred for 30 minutes at 25-30° C. The material is filtered, washed with acetone (30 ml) and then dried to give 29 gm of pure eprosartan mesylate [HPLC Purity: 99.95%; Specific Surface Area: 1.09 m2/g; Mean particle size (D50): 12.13 μm and 90 volume-% of the particles (D90): 33.48 μm].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08361507B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-35f8ef45cea9444dac6cf8153a70d751 |
|---|
| Source note | uspto-grants-2013_01 |
|---|