Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 3-Benzyl-4-chloro-2-methyl-1H-pyrrolo[3,2-c]pyridine | HCID 70700438 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11682399 | HCID 11682399 | 35.2% |
Reaction Steps
Cesium carbonate (85 mg, 0.26 mmol), (S)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (11 mg, 0.020 mmol), tris(dibenzylideneacetone)dipalladium(0) (8 mg, 0.009 mmol), and 4-fluorobenzylamine (0.035 ml, 0.26 mmol) were added to a solution of 3-benzyl-4-chloro-2-methyl-1H-pyrrolo[3,2-c]pyridine (50 mg, 0.17 mmol) prepared in Preparation 2 in toluene (3 ml). The reaction mixture was refluxed under stirring for 2 days. The reaction mixture was cooled to room temperature, filtered, and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography, dissolved in ethyl ether (2 ml), and then saturated with hydrochloric acid gas. The resulting precipitate was filtered to give the titled compound as a white solid. (Yield: 35.2%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513277B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-2080132b164a4d5498adcb518b983113 |
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| Source note | uspto-grants-2013_08 |
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