Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (3-Acetamidophenyl)boronic acid | HCID 157274 | — |
| Reactant | HCID 86665768 | HCID 86665768 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86710174 | HCID 86710174 | 78.8% |
Reaction Steps
To a 100 mL round bottom flask, 4-(7-bromo-2-chloropyrido[3,2-d]pyrimidin-4-yl)morpholine (1.5 g, 0.0045 mol—Preparation 3), 3-acetamidophenylboronic acid (0.769 g, 0.0043 mol), sodium carbonate (1.2 g, 0.0113 mol), toluene (30 mL), ethanol (30 mL) and water (10 mL) were added. The reaction mixture was degassed with N2 for 5-10 minutes. To the same reaction mixture, Pd(PPh3)2Cl2 (0.159 g, 0.00022 mol) was added and again degassed with N2 for 5-10 minutes. The reaction mixture was stirred at 95° C. for 2 hours. The reaction mixture was cooled to room temperature and diluted with ethyl acetate. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure to afford the crude product. The crude product was purified by column chromatography (60-120 silica gel, 60% ethyl acetate in hexane) to provide the title compound (1.3 g, 76%). 1H NMR (300 MHz, DMSO-d6): δ 10.15 (s, 1H), 9.05 (d, J=2.4 Hz, 1H), 8.18 (d, J=2.4 Hz, 1H), 8.11 (s, 1H), 7.46-7.66 (m, 3H), 4.52 (br s, 4H), 3.81 (t, J=5.1 Hz, 4H), 2.09 (s, 3H): LC-MS (ESI): Calculated mass: 383.1; Observed mass [M+H]+: 383.8. (RT=1.31 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145411B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-27c3d2e42fad474eb8d7fdd494bdb232 |
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| Source note | uspto-grants-2015_09 |
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