HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium → 5-[4-[[3-Methyl-4-oxo-3,4-dihydroquinazolin-2-yl]methoxy]benzyl]thiazolidine-2,4-dione potassium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Balaglitazone | HCID 9889200 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 5-[4-[[3-Methyl-4-oxo-3,4-dihydroquinazolin-2-yl]methoxy]benzyl]thiazolidine-2,4-dione potassium salt | HCID 9889199 | 91% |
Reaction Steps
5-[4-[[3-Methyl-4-oxo-3,4-dihydroquinazolin-2-yl]methoxy]benzyl]thiazolidine-2,4-dione (40 g) was dissolved in a mixture of xylene (280 ml) and methanol (280 ml) at reflux temperature to get clear solution. Potassium tertariry butoxide (12.52 g) dissolved in methanol was added slowly drop wise. After complete addition, the reaction mass was stirred at room temperature for 1 hour. The precipitated compound was filtered, washed with methanol and dried the compound in oven at 60-80° C. to yield polymorphic Form 1 of 5-[4-[[3-methyl-4-oxo-3,4-dihydroquinazolin-2-yl]methoxy]benzyl]thiazolidine-2,4-dione potassium salt (40 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377950B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-a6e065b5148d4b4f917a929a03892c51 |
| Source note | uspto-grants-2013_02 |