Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | HCID 57899416 | HCID 57899416 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Product | HCID 57899369 | HCID 57899369 | — |
Reaction Steps
A solution of 3-{5-(4-chloro-phenyl)-4-oxo-6-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-4,5-dihydro-pyrazolo[3,4-d]pyrimidin-1-yl}-benzene sulfonamide (0.300 g, 0.496 mmol) in N,N-dimethylformamide (25 mL) is degassed with argon for 0.5 h. Then 2-amino-5-bromopyridine (0.128 g, 0.745 mmol), cesium carbonate (0.323 g, 0.993 mmol), Pd(dppf)2Cl2 (0.036 g, 0.049 mmol) is added and the resulted mixture is degassed with argon for 0.5 h. The reaction mixture is then heated at 100° C. for 4 h. The reaction mixture is cooled to rt and diluted with water and extracted with ethyl acetate (3×). The combined organic layer is washed with brine, dried over Na2SO4, concentrated, and purified by preparative HPLC to afford 3-[2-[4-(6-amino-pyridin-3-yl)-phenyl]-1-(4-chloro-phenyl)-6-oxo-1,6-dihydro-purin-9-yl]-benzene sulfonamide. 1H NMR (DMSO-d6, 400 MHz) δ 8.66 (s, 1H), 8.23 (s, 1H), 8.07 (m, 1H), 7.94 (m, 1H), 7.83 (m, 1H), 7.67 (m, 1H), 7.58 (m, 2H), 7.35-7.48 (m, 10H), 6.47 (d, 1H), 6.15 (br, 1H); LC-MS calculated for C28H20ClN7O3S (M+H+) 570.1, found 570.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08722691B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-d133dcc7684d46979dfcbd7cf043f3b7 |
|---|
| Source note | uspto-grants-2014_05 |
|---|