HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anthranilic Acid → 2-[(2-Methoxy-pyridin-4-ylmethyl)-amino]-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Methoxypyridine-4-carbaldehyde | HCID 2762996 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[(2-Methoxy-pyridin-4-ylmethyl)-amino]-benzoic acid | HCID 62989484 | — |
Reaction Steps
A mixture of anthranilic acid (1.37 g, 1.0 mmol), 2-methoxy-pyridine-4-carbaldehyde (1.37 g, 1.0 mmol), and p-toluenesulfonic acid mohohydrate (0.025 g, 0.13 mmol) in 30 mL of anhydrous toluene was stirred at reflux for 1 h, cooled to RT, and NaBH4 (0.9 g) was added. The mixture was stirred at RT for 30 min, and quenched with MeOH. The volatiles were removed under reduced pressure, and the residue was taken up in water. AcOH was added to bring pH to 4, and the mixture was extracted with EtOAc. The combined organic portions were washed with brine, dried over MgSO4, filtered, and condensed. The residue was purified by flash column chromatography to give the titled compound. MS (ES+): 259.0 (M+H)+. Calc'd for C14H12N2O3-258.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307088B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-57dc88a6beba4ba48211edb37dfd0171 |
| Source note | uspto-grants-2007_12 |