HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodobenzene → 4-(2-Ethyl-6-fluoro-1-phenyl-1H-indol-3-YL)-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-N,2-N-dimethylcyclohexane-1,2-diamine | HCID 551074 | — |
| Reactant | 4-(2-ethyl-6-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid tert-butyl ester | HCID 58747998 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Ethyl-6-fluoro-1-phenyl-1H-indol-3-YL)-piperidine-1-carboxylic acid tert-butyl ester | HCID 58747999 | 27.3% |
Reaction Steps
To a solution of 4-(2-ethyl-6-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid tert-butyl ester (0.36 g) in degassed toluene (10 ml) at r.t., is added potassium phosphate (0.1 g), copper iodide (20 mg), iodobenzene (254 mg) and N,N′-dimethylcyclohexane-1,2-diamine (30 mg). The mixture is heated at reflux for 3 days. Thereafter the mixture is allowed to cool to r.t., and water (20 ml) added. Ethyl acetate (3×10 ml) is used to extract the organic components and the organic layer is washed with water, dried over MgSO4 and concentrated in vacuo. Flash chromatography (9:1 cyclohexane:ethyl acetate) gives 120 mg pure product (27%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759365B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-6a823c4a5e834d72990614dc4283cd01 |
| Source note | uspto-grants-2010_07 |