Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Chloropurine | HCID 5359277 | — |
| Reactant | (2-(2-Methoxyphenyl)-8-methylquinolin-3-yl)methanol | HCID 57707787 | — |
| Reactant | DABCO purine | HCID 69727605 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178489346 | HCID 178489346 | — |
Reaction Steps
Prepared according to modified Procedure L. 6-Chloropurine (0.077 g, 0.5 mmol, 2 eq) and DABCO (0.112 g, 1 mmol, 4 eq) were stirred in DMSO (0.7 mL) at room temperature for 5 h. In a separate flask, sodium hydride (0.040 g, 1 mmol, 4 eq) was added portion-wise to a stirring solution of (2-(2-methoxyphenyl)-8-methyl-quinolin-3-yl)methanol (0.070 g, 0.25 mmol) in DMSO (0.5 mL), and after 30 minutes, the purine-DABCO salt was added to this mixture. The reaction stirred at room temperature 18 h. 3-((9H-purin-6-yloxy)methyl)-2-(2-methoxyphenyl)-8-methylquinoline [PI3Kδ IC50=38 nM] was isolated as a white solid after purification on a silica column. 1H NMR (400 MHz, DMSO-d6) δ ppm 13.41 (1 H, s), 8.51 (1 H, s), 8.39 (1 H, s), 7.87 (1 H, d, J=7.8 Hz), 7.65 (1 H, d, J=7.0 Hz), 7.49-7.56 (1 H, m), 7.34-7.46 (2 H, m), 7.12 (1 H, d, J=8.2 Hz), 7.03 (1 H, t, J=7.2 Hz), 5.58 (2 H, s), 3.72 (3 H, s), 2.69 (3 H, s) Mass Spectrum (ESI) m/e=398.2 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08901135B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-95e3f4fa3e51488680f46f066b167cee |
|---|
| Source note | uspto-grants-2014_12 |
|---|