Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 44241532 | HCID 44241532 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44465602 | HCID 44465602 | — |
Reaction Steps
2-Bromo-1-(4-hydroxy-phenyl)-1H-indole-3-carbonitrile (Example 1), 1.4 eq pyrrole, 2 eq cesium carbonate and 20 mol % copper(I) iodide was mixed in a oven-dried vial, DMF was added and the mixture was flushed with nitrogen. The vial was sealed and stirred at 120° C. for 48 hours. The reaction-mixture was cooled to rt, diluted with EtOAc and filtered through silica. The crude mixture was evaporated to dryness and subjected to reversed phase preparative HPLC. Appropriate fractions were combined and evaporated, and identified by 1H-NMR and LC/MS. Purity was determined by analytical HPLC. ES/MS m/z: 300.2 (M+H), 298.3 (M−H); 1H NMR (acetone-d6, 500 MHz): 7.74 (m, 1H), 7.41-7.35 (m, 2H), 7.27 (m, 214), 7.23 (m, 1H), 6.98 (m, 214), 6.95 (t, 2H, J=2.2 Hz) and 6.23 (t, 2H, J=2.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367665B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-013e9e6b9cc44569b3bf6d476674aff0 |
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| Source note | uspto-grants-2013_02 |
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