Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hantzsch ester | HCID 70849 | — |
| Reactant | HCID 136388325 | HCID 136388325 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 73455757 | HCID 73455757 | 8.8% |
Reaction Steps
To a stirred suspension of 5-(2-(3,4-dichlorobenzylthio)pyrimidin-4-ylmethylidene)rhodanine (Example 25, 0.3 mmol) in toluene (5 mL) was added diethyl 2,6-dimethyl-1,4-dihydro-3,5-pyridine dicarboxylate (109 mg, 0.39 mmol) and 0.3 g of activated silica gel. The mixture was heated to 80° C. for 20 h then filtered while warm. The filter cake was rinsed with ethyl acetate and the combined filtrates were evaporated to dryness. The residue was redissolved in ethyl acetate and extracted with 1 N aqueous hydrochloric acid. The organic layer was dried (sodium sulfate) and concentrated to give 11 mg of pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518268B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-0829ba0b273b4464b2ee8f317d538e26 |
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| Source note | uspto-grants-2003_02 |
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