Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Formamide | HCID 713 | — |
| Reactant | ethyl 2-amino-5-(4-benzyloxyphenyl)-1H-pyrrole-3-carboxylate | HCID 22936919 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178518056 | HCID 178518056 | — |
Reaction Steps
After adding 84 ml of formic acid, 338 ml of formamide and 169 ml of dimethylformamide to 56.7 g of the ethyl 2-amino-5-(4-benzyloxyphenyl)-1H-pyrrole-3-carboxylate synthesized in Production Example 153-1, the mixture was stirred at 140° C. for 48 hours and then allowed to stand at room temperature for 24 hours. The precipitated solid was filtered out and dried under reduced pressure to obtain 41 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612092B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-53502823f8cd40c9859a6c034eb7c3bb |
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| Source note | uspto-grants-2009_11 |
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