Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Acetylcyclohexanone | HCID 13400 | — |
| Reactant | 6-Bromo-1-methyl-1H-indole | HCID 15546854 | — |
| Reactant | 2-(5-Trifluoromethyl-pyridin-2-YL)-ethylamine | HCID 18071344 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58007491 | HCID 58007491 | 34% |
Reaction Steps
To 2-(5-trifluoromethyl-pyridin-2-yl)-ethylamine (200 mg, 1.05 mmol) was added 6-bromo-1-methyl-1H-indole (685 mg, 2.10 mmol), cuprous iodide (10 mg, 0.05 mmol) and cesium carbonate (685 mg, 2.1 mmol) under an argon atmosphere. Then DMF (400 μl) and 2-acetylcyclohexanone (28 μl, 0.21 mmol) were added and the reaction mixture was stirred for 4 h at 120° C. After cooling to ambient temperature the reaction mixture was separated between tert-butylmethylether (2×20 ml) and water (15 ml). The combined organic layers were washed with brine (15 ml) and dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 67:33) afforded the title compound (114 mg, 34%) as a light brown oil. MS m/e: 320.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133909B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-a1c5a4a7b3c540cab1df63891eb69458 |
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| Source note | uspto-grants-2012_03 |
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