Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Amino-4-bromobenzamide | HCID 13805507 | — |
| Reactant | Trimethyl(phosphooxy)silane | HCID 16133246 | — |
| Reactant | Sodium 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetate | HCID 66609989 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178517774 | HCID 178517774 | 77% |
Reaction Steps
To a mixture of sodium 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetate from Example 2 Step B (2.05 g, 9.62 mmol) and 2-amino-4-bromobenzamide (1.89 g, 8.75 mmol) was added trimethylsilyl polyphosphate (˜15 mL) and the mixture was stirred overnight at 120° C. Equal volumes of EtOAc and water were added and the resulting solution was stirred for 1 h. The EtOAc layer was washed with brine, dried over Na2SO4 and then concentrated under reduced pressure. Et2O was added and evaporated. Trituration of the residue with hexanes, followed by collection of the solid by filtration afforded 7-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)quinazolin-4-ol (2.49 g, 77%). 1H NMR (300 MHz, DMSO-d6) δ 11.37 (s, 1H), 8.76 (s, 1H), 7.97-8.07 (m, 2H), 7.88 (d, J=8.3 Hz, 1H), 7.69-7.81 (m, 2H);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633207B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-892dd47a47fb4d819fccf96d561ff847 |
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| Source note | uspto-grants-2014_01 |
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