Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 3-Bromo-o-toluidine | HCID 123538 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59375063 | HCID 59375063 | 36.2% |
Reaction Steps
A mixture of 1H-benzo[d][1,3]oxazine-2,4-dione (200 mg, 1.226 mmol), 3-bromo-2-methylaniline (228 mg, 1.226 mmol), and trimethoxymethane (390 mg, 3.68 mmol) in THF (2 mL) was heated overnight in a sealed tube at 100° C. The mixture was cooled to rt and concentrated, and the residue was purified by column chromatography (eluting with 90:10 to 50:50 hexane-EtOAc) to give 3-(3-bromo-2-methylphenyl)quinazolin-4(3H)-one (140 mg, 36%). 1H NMR (400 MHz, chloroform-d) δ 8.37 (1 H, dd, J=8.3, 1.2 Hz), 7.97 (1 H, s), 7.76-7.86 (2 H, m), 7.72 (1 H, t, J=4.6 Hz), 7.57 (1 H, ddd, J=8.0, 6.7, 1.5 Hz), 7.21-7.28 (2 H, m), 2.26 (3 H, s). Mass spectrum m/z 315, 317 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-30735fbbf8154dc9b3f625343ba1220b |
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| Source note | uspto-grants-2013_01 |
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