Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 57443413 | HCID 57443413 | — |
| Reactant | HCID 178514655 | HCID 178514655 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 11164862 | HCID 11164862 | 46% |
Reaction Steps
7 mg of compound (i) prepared by the above Step 2 was dissolved in methanol solution (0.02 mmol) and then 1.7 M methanolic suspension solution containing NH2OK (0.4 ml, 0.68 mmol) was added thereto at 0° C. and the resulting mixture was stirred for 8 hrs at room temperature. The resulting mixture was neutralized with 0.01 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 3.2 mg of N-{4-[3-(2-hydroxycarbamoyl-ethyl)-2-oxo-2,5-dihydro-pyrrole-1-yl-methyl]-phenyl}-benzamide (j) (yield: 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846963B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-b74c37d68e274b5189be225b63f2531f |
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| Source note | uspto-grants-2010_12 |
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