Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propan-2-ol | HCID 46738028 | — |
| Reactant | HCID 86670145 | HCID 86670145 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 60197474 | HCID 60197474 | 68.8% |
Reaction Steps
A mixture of (R)-2-(2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)-N-((tetrahydro-2H-pyran-4-yl)methyl)acetamide (PREPARATION x26, 50 mg, 0.131 mmol), 2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ol (51.5 mg, 0.196 mmol), tetrakis(triphenylphospine)palladium (0) (15.13 mg, 0.013 mmol) and sodium carbonate (27.8 mg, 0.262 mmol) in 1,4-dioxane (0.5 mL) and H2O (0.25 mL) was heated to 120° C. in a microwave for 1 hour. After cooling to room temperature, the reaction mixture was diluted with EtOAc, washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography (amine-functionalized silica, 0-10% MeOH gradient in CHCl3) to afford the title compound as an off-white solid (43.4 mg, 0.090 mmol, 68.8%). 1H NMR (400 MHz, DMSO-d6) δ 1.06-1.26 (m, 2 H), 1.45 (s, 6 H), 1.48-1.71 (m, 3 H), 2.91-3.05 (m, 3 H), 3.11-3.36 (m, 5 H), 3.50-3.67 (m, 2 H), 3.73-3.93 (m, 4 H), 3.96-4.09 (m, 2 H), 4.56 (d, J=11.87 Hz, 1 H), 5.04 (s, 1 H), 7.31 (t, J=7.71 Hz, 1 H), 7.40-7.47 (m, 1 H), 7.51 (s, 1 H), 7.99-8.12 (m, 2 H), 8.34 (s, 1 H). ESI-MS m/z [M+H]+ calc'd for C26H35N5O4, 481.27; found 482.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045496B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-da20d0d2d436419694499375edf69295 |
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| Source note | uspto-grants-2015_06 |
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