Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 262601-94-5 | HCID 3114247 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21936681 | HCID 21936681 | 16% |
Reaction Steps
To a solution of 5-pyridin-2-ylmethylene-thiazolidine-2,4-dione (5.0 g, 0.024 mol, prepared in a similar way as described in J. Med. Chem. 41 (10), 1619–1630 (1998)) in tetrahydrofuran (300 ml) was added 10% palladium on carbon (1 g) and the resulting mixture was hydrogenated. After 50 ml of hydrogen was consumed and additional portion of 10% palladium on carbon (5 g) was added and the hydrogenation was continued at 50 psi for 16 hours. The mixture was filtered and the filtrate evaporated in vacuo. The residue was subjected to flash column chromatography (1 I silicagel) using a mixture of ethyl acetate/hexane (1:1) as eluent. Semi pure fractions were collected and the solvent evaporated in vacuo affording 0.8 g (16%) of 5-pyridin-2-ylmethyl-thiazolidine-2,4-dione as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019026B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-2bbab47e676949c3b426a65c92b5031b |
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| Source note | uspto-grants-2006_03 |
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