Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21098393 | HCID 21098393 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 11174663 | HCID 11174663 | — |
Reaction Steps
To a solution of 5-allyl-7-methoxy-4-phenylamino-quinazolin-6-ol (0.16 g, 0.524 mmol) (from Example 15, Step D, supra) in acetone (30 mL) was added K2CO3 (0.36 g, 2.62 mmol) and methyl iodide (0.15 g, 1.05 mmol) (Aldrich). The reaction mixture was heated with stirring at 90° C. for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using EtOAc/CH2Cl2/Et3N (1:5:0.05) as eluent to give the desired (5-allyl-6,7-dimethoxy-quinazolin-4-yl)-phenyl-amine as a pale yellow solid. (Yield 0.13 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217717B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-dae9a2ec8d2e499bbf204467a9e322e0 |
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| Source note | uspto-grants-2007_05 |
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