Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Iodopyrazine | HCID 642841 | — |
| 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 57899359 | HCID 57899359 | — |
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 (prepared as described in example 38, 0.75 g, 1.2 mmol) in N,N-dimethylformamide (20 mL) is degassed with argon for 0.5 h. Then 2-iodopyrazine (0.38 g, 1.86 mmol), cesium carbonate (0.81 g, 2.4 mmol), Pd(dppf)2Cl2 (0.09 g, 0.12 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 column chromatography to afford 1-(4-chloro-phenyl)-9-(3-methanesulfonyl-phenyl)-2-(4-pyrazin-2-yl-phenyl)-1,9-dihydro-purin-6-one. 1H NMR (DMSO-d6, 400 MHz) δ 9.24 (m, 1H), 8.77 (s, 1H), 8.70 (s, 1H), 8.62 (s, 1H), 8.45 (s, 1H), 8.25 (d, 1H), 8.04 (m, 3H), 7.90 (m, 1H), 7.54 (m, 2H), 7.43 (m, 4H), 3.3 (s, 3H); LC-MS calculated for C28H19ClN6O3S (M+H+) 555.1, found 555.0.
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-2a9d1ef56ad94470b9d8a79b5122b4b8 |
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| Source note | uspto-grants-2014_05 |
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