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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Ethyl orthopropionate | HCID 66995 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Quinazolone, 2-ethyl-3-methyl | HCID 325352 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642609B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-97c11e7a34ee47ec9dd9c94908815b36 |
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| Source note | uspto-grants-2014_02 |
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