HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591581Generated: October 25, 2026
2-Bromopyridine → 2-bromo-9-(pyridin-2-yl)-9H-carbazole
https://huagongshe.com/reaction/591581
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | 2-Bromo-9H-carbazole | HCID 12717089 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | 2-bromo-9-(pyridin-2-yl)-9H-carbazole | HCID 70654852 | 70% |
Reaction Steps
Under a nitrogen atmosphere, 10 mmol of 2-bromo-9H-carbazole, 15 mmol of 2-bromopyridine, 1 mmol of copper(I)iodide, 25 mmol of potassium carbonate, and 2 mmol of L-proline were combined in stirring degassed dimethyl sulfoxide. The mixture was heated to 90° C. for 3 days before being cooled and separated between dichloromethane and water. The water layer was washed twice with dichloromethane and the organics were combined and washed once with brine. The organic fraction was dried with magnesium sulfate and concentrated under reduced pressure and subjected to column chromatography of silica with dichloromethane as the eluent. After concentrating under reduced pressure, 2-bromo-9-(pyridin-2-yl)-9H-carbazole was isolated in a 70% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238668B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-cc2bb602808b4751af18670f5fc69de2 |
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| Source note | uspto-grants-2016_01 |
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