Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| 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 11524132 | HCID 11524132 | 41.2% |
Reaction Steps
Cesium carbonate (93 mg, 0.28 mmol), (S)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (12 mg, 0.021 mmol), tris(dibenzylideneacetone)dipalladium(0) (9 mg, 0.010 mmol), and 4-chlorobenzyl alcohol (0.039 ml, 0.28 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 and then recrystallized in n-hexane (3 ml). The resulting solid was dissolved in ethyl ether (2 ml), saturated with hydrochloric acid gas, and then filtered to give the titled compound as a white solid. (Yield: 41.2%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148529B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-0cf2377c08a8478b8e14de59fff8ab64 |
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| Source note | uspto-grants-2012_04 |
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