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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039525Generated: November 3, 2026

Anthranilic Acid → 2-(3-Nitro-benzyl)-benzo[d][1,3]oxazin-4-one

https://huagongshe.com/reaction/2039525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
ReactantPyridineHCID 1049—
Reactant3-Nitrobenzeneacetyl chlorideHCID 523225—
SolventDichloromethaneHCID 6344—
Product2-(3-Nitro-benzyl)-benzo[d][1,3]oxazin-4-oneHCID 67043000—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of commercially available (3-nitro-phenyl)-acetyl chloride (2.20 g, 11.05 mmol) in anhydrous DCM (9 mL) was added 2-aminobenzoic acid (0.76 g, 5.50 mmol). Pyridine (3 mL) was then added to the mixture and the reaction mixture was heated under microwave condition at 120° C. for 30 minutes, then diluted with dichloromethane and washed with NaHCO3 satured solution, then with water followed by brine. The organic phase was dried over Na2SO4, filtered and evaporated to give the 2-(3-nitro-benzyl)-benzo[d][1,3]oxazin-4-one intermediate as red oil. To a solution of 2-(3-nitro-benzyl)-benzo[d][1,3]oxazin-4-one in dry pyridine (10 mL) was added aminoguanidine hydrogencarbonate (0.90 g, 6.60 mmol) and the mixture was heated under microwave condition at 180° C. for 20 minutes. The solvent was then evaporated and the crude was purified by flash column chromatography on silica gel eluting with DCM/CH3OH 95/5 to afford the title compound as orange solid (0.35 g, 30% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580783B2
Source datasetuspto-grants-2013_11
ORD IDord-969513d945814eb38403fe0f917342b9
Source noteuspto-grants-2013_11