HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2-Methyl-1H-imidazo[4,5-c]pyridin-1-yl)benzonitrile | HCID 10681187 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid | HCID 10467437 | 70% |
Reaction Steps
A mixture of 4-(2-methylimidazo[4,5-c]pyrid-1-yl)benzonitrile (see EP-0310386) (12.0 g, 51.3 mmol) and sodium hydroxide (22.0 g, 0.55 mmol) in a mixture of ethanol (55 ml) and water (55 ml) was heated under nitrogen at reflux for 1.5 hours, cooled and concentrated under reduced pressure. The brown residue was dissolved in ice-water and glacial acetic acid (33 ml) was added. The resulting precipitate was collected, washed with water and dried under vacuum at 70° C. to give the title compound (9.1 g, 70%) as a buff coloured solid which as characterised by its 1H-NMR spectrum. 1H NMR (DMSO-d6), 2.50(3H,s), 7.25(1H,d,J=5 Hz), 7.72(2H,d,J=8 Hz), 8.16(2H,d,J=8 Hz), 8.30(1H,d,J=5 Hz), 8.92(1H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05358953 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-7d5b5d729fa94174acd419ddb0416c71 |
| Source note | uspto-grants-1994_10 |