Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 67453428 | HCID 67453428 | — |
| Reactant | HCID 178514655 | HCID 178514655 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 71460963 | HCID 71460963 | 50% |
Reaction Steps
100 mg of 3-[2-oxo-1-(3-p-tolyl-propyl)-2,5-dihydro-1H-pyrrol-3-yl]-propionic acid methyl ester (40ag) prepared by the above Step 7 was dissolved in methanol solution (0.33 mM) and then 1.7 M methanolic suspension solution containing NH2OK (0.82 ml, 5.0 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 50 mg of N-hydroxy-3-[2-oxo-1-(3-p-tolyl-propyl)-2,5-dihydro-1H-pyrrol-3-yl]-propionamide (40ah) (yield: 50%).
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-ae01b94e4f7747f8856f6bdf5e4f6ef5 |
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| Source note | uspto-grants-2010_05 |
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