HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056077Generated: October 26, 2026
Butyl vinyl ether → 8-(1-butoxyvinyl)-N-phenylquinazolin-2-amine
https://huagongshe.com/reaction/1056077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl vinyl ether | HCID 8108 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | 8-bromo-N-phenylquinazolin-2-amine | HCID 89781929 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-(1-butoxyvinyl)-N-phenylquinazolin-2-amine | HCID 89781904 | 67% |
Reaction Steps
A solution of 8-bromo-N-phenylquinazolin-2-amine (310.3 mg, 1.034 mmol), diacetoxypalladium (23.21 mg, 0.103 mmol), potassium carbonate (286 mg, 2.068 mmol), 1,3-bis(diphenylphosphino)propane (94 mg, 0.227 mmol), and 1-(vinyloxy)butane (0.147 mL, 1.137 mmol) in a mixture of DMF (4.0 mL) and water (0.800 mL) was stirred under argon in a sealed tube at 70° C. for 3 d. The mixture was adsorbed onto silica gel (DMF was removed in vacuo). Chromatographic purification (silica gel, 0-50% EtOAc/hexanes, 20 min, 254 nm) furnished 8-(1-butoxyvinyl)-N-phenylquinazolin-2-amine (220 mg, 0.689 mmol, 67% yield) as a yellow solid: 1H NMR (400 MHz, CDCl3) δ ppm 9.06 (1H, s), 7.95 (1H, s), 7.90 (2H, d, J=8.2 Hz), 7.68 (1H, d, J=8.0 Hz), 7.34-7.37 (2H, m), 7.33 (1H, br. d, J=3.8 Hz), 7.31 (1H, d, J=7.8 Hz), 7.05 (1H, t, J=7.3 Hz), 4.99 (1H, d, J=1.0 Hz), 4.64 (1H, s), 3.99 (2H, t, J=6.7 Hz), 1.81 (2H, quin, J=7.1 Hz), 1.50 (2H, sxt, J=7.5 Hz), 0.96 (3H, t, J=7.4 Hz). m/z (ESI, +ve) 320.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394297B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a529f403e3dc411ba92271698b64645f |
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| Source note | uspto-grants-2016_07 |
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