HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712372Generated: October 29, 2026
Methanol → 6,7-Dimethoxy-3H-quinazolin-4-one
https://huagongshe.com/reaction/712372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 4,5-Dimethoxyanthranilic acid | HCID 79736 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,7-Dimethoxy-3H-quinazolin-4-one | HCID 135495016 | 93% |
Reaction Steps
A suspension of 2-amino-4,5-dimethoxybenzoic acid (23.40 g), trimethoxymethane (52 mL), ammonium formate (30.00 g) and methanol (400 mL) was heated to 70° C. and refluxed for 4 h. After the reaction mixture was cooled to room temperature, 160 mL of water was added to the reaction. The mixture was filtered to afford the title compound as a yellow solid (22.70 g, 93.00%). The compound was characterized by the following spectroscopic data: 1H NMR (400 MHz, d6-DMSO) δ: 3.87 (s, 3H), 3.91 (s, 3H), 7.13 (s, 1H), 7.45 (s, 1H), 7.98 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181277B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-45f80623c03f4f24846c106a70b5c2d2 |
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| Source note | uspto-grants-2015_11 |
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