Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 57443418 | HCID 57443418 | — |
| Reactant | HCID 178514655 | HCID 178514655 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 11162137 | HCID 11162137 | 65% |
Reaction Steps
38 mg of 3-{1-[2-(2-fluoro-phenyl)-ethyl]-2-oxo-2,5-dihydro-1H-pyrrol-3-yl}-propionic acid methyl ester (x) prepared by the above Step 4 was dissolved in methanol solution (0.13 mM) and then 1.7 M methanolic suspension solution containing NH2OK (0.38 ml, 0.65 mM) was added thereto at 0° C. and the resulting mixture was stirred for 8 hrs at room temperature. The resulting mixture was neutralized with 0.02 ml of acetic acid, diluted with 10% methanol/chloroform solution, filtered and concentrated in vacuo. The resulting compound was purified by Silica gel column chromatography with a solvent mixture mixed with methanol and chloroform (1:9) as an eluant to give 25 mg of 3-{1-[2-(2-fluoro-phenyl)-ethyl]-2-oxo-2,5-dihydro-1H-pyrrol-3-yl}-N-hydroxy-propionamide (28y) (yield: 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723376B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-25de813544d841989cbdddb8cf454e23 |
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| Source note | uspto-grants-2010_05 |
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