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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969695Generated: November 1, 2026

Anthranilic Acid → 2-[(2-Methylamino-pyrimidin-4-ylmethyl)-amino]-benzoic acid

https://huagongshe.com/reaction/969695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(Methylamino)pyrimidine-4-carbaldehydeHCID 22002531—
SolventTolueneHCID 1140—
Product2-[(2-Methylamino-pyrimidin-4-ylmethyl)-amino]-benzoic acidHCID 69512512—

Reaction Steps

A mixture of anthranilic acid (0.55 g, 4.0 mmol), 2-methylamino-pyrimidine-4-carbaldehyde (Step B, 0.72 g, 5.2 mmol), and p-toluenesulfonic acid mohohydrate (0.025 g, 0.13 mmol) in 20 mL of anhydrous toluene was stirred at reflux for 1 h, and cooled to RT. NaBH4 (0.41 g, 10.8 mmol) was added, and the mixture was stirred at RT for 30 min. The mixture was quenched with MeOH, the volatiles were removed under reduced pressure, and the residue was taken up in water. AcOH was added to bring the pH to 4 and the mixture was extracted with EtOAc. The combined organic portions were washed with brine, dried over MgSO4, filtered, condensed, and the residue was purified by flash column chromatography to give the titled compound. MS (ES+): 259.0 (M+H)+. Calc'd for C13H14N4O2-258.28

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307088B2
Source datasetuspto-grants-2007_12
ORD IDord-b7f62077799342e6be111383539a4bee
Source noteuspto-grants-2007_12