Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamidine | HCID 68047 | — |
| Reactant | HCID 10825232 | HCID 10825232 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178488440 | HCID 178488440 | 11.5% |
Reaction Steps
Ethyl 3-amino-5-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate (7.2 g) was dissolved in tetrahydrofuran (16 mL)/ethanol (32 mL), formamidine (3.46 g) was added, and the mixture was stirred at 90° C. for 16 hrs. After cooling to room temperature, tetrahydrofuran was evaporated under reduced pressure. The residue was diluted with ethanol (20 mL), and the precipitated powder was collected by filtration, washed with ethanol (15 mL) and dried under reduced pressure to give the title compound (769 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08178543B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-d468f2b86fb242b98d107f23159ae0e0 |
|---|
| Source note | uspto-grants-2012_05 |
|---|