HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729410Generated: October 25, 2026
Sodium hydride → 3-Amino-1-cyclopropyl-6,7-difluoro-1H-quinazoline-2,4-dione
https://huagongshe.com/reaction/729410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | O-(2,4-dinitrophenyl)hydroxylamine | HCID 87140 | — |
| Reactant | 1-Cyclopropyl-6,7-difluoroquinazoline-2,4(1H,3H)-dione | HCID 11276448 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Amino-1-cyclopropyl-6,7-difluoro-1H-quinazoline-2,4-dione | HCID 11482177 | 63.8% |
Reaction Steps
To a solution of 1-cyclopropyl-6,7-difluoro-1H-quinazoline-2,4-dione (Example 23a, 2.0 g, 8.92 mmol) in dioxane (7.5 mL) and dimethylformamide (7.5 mL) is added NaH (60% dispersion in oil, 428 mg, 10.7 mmol). The solution is heated to 60° C. for 10 minutes and cooled to room temperature. To the cooled solution is added O-(2,4-dinitrophenyl)hydroxylamine (1.77 g, 8.92 mmol), and the solution is heated to 80° C. for 30 minutes. The resulting red solution is cooled to room temperature, poured over crushed ice, and extracted with EtOAc. The combined organic layers are dried over MgSO4, filtered, and the solvent removed under reduced pressure. The resulting solid is triturated with Et2O and air dried to afford 1.44 g of the title compound. MS CI: m/z 254 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582627B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-fcf64d84b84f45a1a5f9c9eb388a411f |
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| Source note | uspto-grants-2009_09 |
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