Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 43155822 | HCID 43155822 | — |
| Reactant | Ethyl-2-(5-oxo-2-thioxoimidazolidin-1-yl)acetate | HCID 43995697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86675361 | HCID 86675361 | 43.6% |
Reaction Steps
5-(3-Iodophenyl)furan-2-carbaldehyde (30 mg, 0.1 mmol) synthesized by the same method as in Example 1 and ethyl-2-(5-oxo-2-thioxoimidazolidin-1-yl)acetate (20 mg, 0.1 mmol) were dissolved in dichloromethane (7 mL), piperidine (20 μL) was added thereto, and the mixture was stirred at room temperature (25° C.) overnight. After the reaction was completed the solvent was removed by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography using ethyl acetate/hexane (3/7 (volume ratio)) as an eluent, to give compound 2 in a yield of 21 mg (yield 43.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476449B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8b5708c1b379492382885c12243bcee2 |
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| Source note | uspto-grants-2013_07 |
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