Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18005067 | HCID 18005067 | 67.9% |
Reaction Steps
A suspension of compound 1 (195 mg, 1.20 mmol), 3-Bromopyridine (98 μL, 1.00 mmol), copper iodide (9.5 mg, 0.05 mmol) and K3PO4 (400 mg, 2.10 mmol) in toluene (6 mL) was treated with N,N′-dimethylethylenediamine (21.5 μL, 0.20 mmol) then heated at 110° C. overnight. A TLC analysis indicated mostly starting indole and 3-bromopyridine and a new more polar spot. The reaction mixture was treated with additional copper iodide ((9.5 mg, 0.05 mmol) and N,N′-dimethylethylenediamine (21.5 μL, 0.20 mmol). The mixture was heated at 110° C. for 7 hours. After cooling, the mixture was poured into H2O (20 mL) then extracted with CH2Cl2 (100 mL). The organic layer was separated, washed with brine and concentrated to give a yellow solid which was subjected to flash chromatography on silica gel (CH2Cl2 to MeOH:CH2Cl2, 5:95) to give compound 72 (195 mg, 67.9%) as a yellow solid. 1H NMR (DMSO-d6) δ 8.90 (d, J=2.4 Hz, 1H), 8.70-8.69 (m, 2H), 8.16-8.07 (m, 2H), 7.99 (d, J=3.2 Hz, 1H), 7.71-7.65 (m, 2H), 7.05 (d, J=3.3 Hz); ESI-MS (m/z, %): 240 (M+1, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989447B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4f849f1d3387499faecd3dfcc313eb75 |
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| Source note | uspto-grants-2011_08 |
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