HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969677Generated: October 30, 2026
Anthranilic Acid → 2-[(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-amino]-benzoic acid
https://huagongshe.com/reaction/969677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1H-Pyrrolo[2,3-b]pyridine-3-carbaldehyde | HCID 5372812 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-amino]-benzoic acid | HCID 66415425 | — |
Reaction Steps
A mixture of anthranilic acid (1.37 g, 1.0 mmol), 1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (1.46 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. After being cooled to RT, NaBH4 (0.9 g) was added, and the mixture was stirred at RT for 30 min. The reaction was quenched with MeOH, and the volatiles were removed under reduced pressure. 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+): 268.1 (M+H)+. Calc'd for C15H13N3O2-267.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307088B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-55702dab23e34f6fb3ccd5bb45c9a4e9 |
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| Source note | uspto-grants-2007_12 |
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