Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Rosiglitazone | HCID 77999 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 9911750 | HCID 9911750 | 84.1% |
Reaction Steps
Methanesulfonic acid (1.69 g) was added to a suspension of 5-[4-[2-(N-methyl-N-(2-pyridyl)amino)ethoxy]benzyl]thiazolidine-2,4-dione (6.0 g) and ethanol (50 ml) and the mixture was stirred and heated to give a clear solution. Diethyl ether (50 ml) was added and the mixture was heated to reflux and then cooled to 21° C. over a period of 1 hour. The product was collected by filtration, washed with diethyl ether (50 ml) and dried under vacuum for 2 hours at 21° C. to give 5-[4-[2-(N-methyl-N-(2-pyridyl)amino)ethoxy]benzyl]thiazolidine-2,4-dione methanesulfonate (6.40 g) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291740B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-a86b5272f43249bba3da29fd1b6b9bcd |
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| Source note | uspto-grants-2007_11 |
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