Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 6-Bromopyridin-3-amine | HCID 642811 | — |
| Reactant | HCID 57899417 | HCID 57899417 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57899367 | HCID 57899367 | — |
Reaction Steps
A solution of 1-(4-chloro-phenyl)-9-(3-methanesulfonyl-phenyl)-2-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1,9-dihydro-purin-6-one (8, 0.21 g, 0.348 mmol) in N,N-dimethylformamide (15 mL) is degassed with argon for 0.5 h. Then 5-amino-2-bromopyridine (0.090 g, 0.52 mmol), cesium carbonate (0.227 g, 0.696 mmol), Pd(dppf)2Cl2 (0.025 g, 0.035 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 2 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 2-[4-(5-amino-pyridin-2-yl)-phenyl]-1-(4-chloro-phenyl)-9-(3-methanesulfonyl-phenyl)-1,9-dihydro-purin-6-one. 1H NMR (CD3OD, 400 MHz) δ 8.63 (s, 1H), 8.56 (s, 1H), 8.23 (d, 1H), 8.09 (d, 1H), 7.95 (s, 1H), 7.86-7.90 (m, 2H), 7.68-7.71 (m, 2H), 7.59 (m, 3H), 7.39 (m, 2H), 7.34 (m, 2H), 3.21 (s, 3H); LC-MS calculated for C29H21ClN6O3S (M+H+) 569.1, found 569.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722691B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-8d1db6fdbbab4f788505cae08fa03c8f |
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| Source note | uspto-grants-2014_05 |
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