Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86628818 | HCID 86628818 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86628819 | HCID 86628819 | — |
Reaction Steps
A mixture of 1-(4-trifluoromethoxyphenyl)-2-ethoxycarbonylmethyl-5-(5-trifluoromethyl-2-pyridinyloxy)indole-3-carboxylic acid ethyl ester (80 mg, 0.13 mmol, see step (a) above), NaOH (aq, 1 M, 1.1 mL), EtOH (0.5 mL) and THF (0.5 mL) was stirred at 100° C. for 9 h, cooled, diluted with H2O and acidified to pH 5 with citric acid (aq, 1 M). The precipitate was collected, washed with H2O and Et2O to give the title compound, 30 mg (42%), mp 203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08097623B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-2b9ad317ff804c3d90b19fe9b53111d4 |
|---|
| Source note | uspto-grants-2012_01 |
|---|