HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(2-Fluoro-4-iodoanilino)-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-(2-fluoro-4-iodoanilino)-6-oxo-1,6-dihydro-3-pyridinecarboxylate | HCID 23630800 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Fluoro-4-iodoanilino)-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid | HCID 23631007 | 99% |
Reaction Steps
Ethyl 4-(2-fluoro-4-iodoanilino)-6-oxo-1,6-dihydro-3-pyridinecarboxylate was dissolved in EtOH and treated with 1 M NaOH, as for example 1, step C, to hydrolyse the ester to give 4-(2-fluoro-4-iodoanilino)-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid as a white solid (99%), used directly in the next step. 1H NMR [(CD3)2SO, 400 MHz] δ 13.30 (v br s, 1H), 11.44 (br s, 1H), 9.75 (br s, 1H), 8.06 (s, 1H), 7.76 (dd, J=10.2, 1.9 Hz, 1H), 7.59 (ddd, J=8.3, 1.9, 0.9 Hz, 1H), 7.32 (t, J=8.4 Hz, 1H), 5.40 (d, J=1.1 Hz, 1H). LCMS (APCI+) calcd for C12H9FIN2O3 375 (MH+), found 375.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07273877B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-f973cebd13a0453e934d82bafaad8f5e |
| Source note | uspto-grants-2007_09 |