HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydroxide ethanol → 6-Iodoquinoxaline-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydroxide ethanol | HCID 23692425 | — |
| Reactant | Ethyl 6-iodoquinoxaline-2-carboxylate | HCID 53485588 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Iodoquinoxaline-2-carboxylic acid | HCID 58152020 | 91% |
Reaction Steps
A solution of compound 9 (1.30 g, 3.96 mmol) in a 2.0 N sodium hydroxide/ethanol solution (1/1, v/v, 6 mL) was refluxed for 30 min. After cooling to room temperature, the reaction mixture was acidified (pH=4-5) with acetic acid and cooled to 0° C. The resulting precipitate was removed by filtration and dried in a vacuum oven to afford acid 23 (1.08 g, 3.29 mmol) as a white solid. Yield 91%; mp 242-244° C.; 1H NMR (200 MHz, DMSO-d6) δ 7.97 (d, 1H, J=8 Hz), 8.15 (d, 1H, J=8 Hz), 8.52 (s, 1H), 9.36 (s, 1H); ESI-MS m/z 298.6 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09125937B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-96c2f833406e4fe2985535c3e6cc06cd |
| Source note | uspto-grants-2015_09 |