Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Hydroxymethyl)benzeneboronic acid | HCID 2734706 | — |
| Reactant | HCID 86670145 | HCID 86670145 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68195143 | HCID 68195143 | 32% |
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), 4-(hydroxymethyl)phenylboronic acid (29.8 mg, 0.196 mmol), tetrakis(triphenylphosphine)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 water (0.25 mL) was heated to 120° C. for 1 hour in a microwave. 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 (silica-NH, gradient 0-10% MeOH/CHCl3) to afford a white solid, which was recrystallized from EtOH/EtOAc to give the title compound as an off-white solid (19.0 mg, 32.0%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.02-1.21 (m, 2 H), 1.48-1.71 (m, 3 H), 2.91-3.02 (m, 3 H), 3.12-3.32 (m, 5 H), 3.50-3.67 (m, 2 H), 3.73-4.08 (m, 6 H), 4.49-4.61 (m, 3 H), 5.19 (t, J=5.68 Hz, 1 H), 7.34 (d, J=8.59 Hz, 2 H), 7.47-7.51 (m, 1 H), 8.08 (t, J=5.94 Hz, 1 H), 8.16 (d, J=8.34 Hz, 2 H); ESI-MS m/z [M+H]+ calc'd for C24H31N5O4, 454.24; found 454.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09045496B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-b30ce3b7e13041c7a332c7cc0b0947cf |
|---|
| Source note | uspto-grants-2015_06 |
|---|