Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Laquinimod | HCID 54677946 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Laquinimod Sodium | HCID 23697158 | 75.4% |
Reaction Steps
N-Ethyl-N-phenyl-1,2-dihydro-4-hydroxy-5-chloro-1-methyl-2-oxoquinoline-3-carboxamide (35 gm) was suspended in ethanol (140 ml) at 20-25° C. under stirring followed by the addition of freshly prepared sodium hydroxide solution (4.13 gm of sodium hydroxide in 11 ml of water) at 20-25° C. and then stirred for 15-30 minutes at 25-30° C. The resulting solution was filtered through a hyflow super cell bed and the bed was washed with ethanol (105 ml) at 25-30° C. The resulting filtrate was seeded with pure laquinimod sodium (0.175 gm) and then stirred for 4 hours at 25-30° C. The resulting mass was cooled to 0-5° C. followed by stirring for 2 hours at the same temperature. The resulting white colored solid was filtered, washed with chilled ethanol (38 ml) and then dried under vacuum at 60-65° C. to yield 28 gm of laquinimod sodium in crystalline Form A1 (HPLC Purity: 99.9%; Bulk density: 0.333 g/ml; Tapped density: 0.476 g/ml; and Particle size distribution: d(0.9)=26.3 microns).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354428B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-d118fbb9f1694295896fbb42178053a1 |
|---|
| Source note | uspto-grants-2013_01 |
|---|