Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 58859188 | HCID 58859188 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58859151 | HCID 58859151 | — |
Reaction Steps
To a solution of 3-benzyloxy-5-(2,2-dimethylpropionyl)-4-oxo-4H-pyran-2-carboxylic acid 3-chlorobenzylamide (113 mg) in tetrahydrofuran (0.7 ml)-ethanol (0.7 ml) was added 2-aminoethanol (0.015 ml) and the mixture was stirred at 60° C. for 11 hr. The solvent was evaporated and the obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:1) to give 3-benzyloxy-5-(2,2-dimethylpropionyl)-1-(2-hydroxyethyl)-4-oxo-1,4-dihydropyridine-2-carboxylic acid 3-chlorobenzylamide (91 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211572B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-924855d5df324e4891ebcd41b9c91726 |
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| Source note | uspto-grants-2007_05 |
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