Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59852996 | HCID 59852996 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ammonium hydroxide methanol | HCID 21894508 | — |
| Product | HCID 59853019 | HCID 59853019 | 31% |
Reaction Steps
A mixture of N-(4-(2-chloropyrimidin-4-yloxy)-3-fluorophenyl)acetamide (100 mg, 0.36 mmol), 4-fluoroaniline (Aldrich, 40 mg, 0.36 mmol), and 1,4-dioxane (3 mL) was heated at reflux for 2 h. The mixture was concentrated in vacuo and the residue triturated with ether to give a gray solid. The product was dissolved in MeOH, treated with silica gel (150 mg) and the mixture concentrated to dryness. The compound was concentrated down on silica gel and applied to a silica gel column and eluted first with EtOAc then with 100:1 MeOH/NH4OH in CH2Cl2 to give the title compound (40 mg, 31%) as a white solid. 1H NMR (DMSO-d6) δ 10.19 (s, 1H), 9.61 (s, 1H), 8.33 (d, 1H, J=5.6 Hz), 7.71 (d, 1H, J=12.7 Hz), 7.40 (s, 2H), 7.30-7.26 (m, 2H), 6.86 (dd, 2H, J=8.3, 8.3 Hz), 6.50 (d, 1H, J=5.4 Hz), 2.05 (s, 3H); MS (ESI+) m/z 357.13 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989477B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-f7d98e0974434d55adc691959d7d9847 |
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| Source note | uspto-grants-2011_08 |
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