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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238199Generated: October 30, 2026

Anthranilic Acid → 4-Quinazolone, 2-ethyl-3-methyl

https://huagongshe.com/reaction/238199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantMethylamineHCID 6329—
ReactantEthyl orthopropionateHCID 66995—
SolventSodium HydroxideHCID 14798—
Product4-Quinazolone, 2-ethyl-3-methylHCID 32535273%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of anthranilic acid (13.7 g, 100 mmol), methylamine (2M solution in methanol, 100 mL, 200 mmol), triethylorthopropionate (40 mL, 200 mmol), pTSA (catalytic amount) was heated at 70° C. with stirring for 3 days. The reaction mixture was cooled to room temperature, IN NaOH solution (160 mL) was added and the mixture stirred vigourously. The resulting precipitate was filtered, washed with water and dried under high vacuum to yield the product as a fluffy white solid (13.67 g, 73%). 1H NMR (400 MHz, CDCl3) δ 1.41 (t, 3H, J=7.4 Hz), 2.87 (q, 2H, J=7.4 Hz), 3.64 (s, 3H), 7.44 (t, 1H, J=8.1 Hz), 7.65 (dd, 1H, J=8.8, 0.7 Hz), 7.72 (t, 1H, J=8.4 Hz), 8.27 (dd, 1H, J=9.2, 1.8 Hz); ESI-MS m/z 189.0 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642609B2
Source datasetuspto-grants-2014_02
ORD IDord-97c11e7a34ee47ec9dd9c94908815b36
Source noteuspto-grants-2014_02