Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | HCID 136337206 | HCID 136337206 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 86644569 | HCID 86644569 | — |
Reaction Steps
To flask containing the title compound from Example 8 Step C (415 mg, 0.971 mmol) were added cesium carbonate (791 mg, 2.43 mmol), 4-bromobenzyl bromide (316 mg, 1.26 mmol), and DMF (6 mL), and the resulting mixture was stirred at 45° C. After 3 h, the reaction mixture was allowed to cool to room temperature, then was poured into brine and extracted with EtOAc. The organic phase was separated and concentrated in vacuo. Purification by chromatography on silica gel (0 to 25% EtOAc in hexanes, then 25 to 100% EtOAc in hexanes) provided the title compound: LCMS m/z 597.7 [M+H]+; 1H NMR (500 MHz, CDCl3) δ 8.21 (s, 1H), 8.05 (d, J=8.0 Hz, 1H), 7.86 (t, J=8.0 Hz, 1H), 7.82 (dd, J=8.0, 2.0 Hz, 1H), 7.49-7.47 (m, 2H), 7.38-7.35 (m, 2H), 7.23 (d, J=8.5 Hz, 2H), 7.11-7.08 (m, 1H), 7.02 (d, J=8.5 Hz, 1H), 5.09 (s, 2H), 4.37 (q, J=7.0 Hz, 2H), 1.38 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507512B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-cb893e91bc44436eb126752290dcb146 |
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| Source note | uspto-grants-2013_08 |
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