HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620064Generated: October 30, 2026
Pyrrole → tert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamate
https://huagongshe.com/reaction/1620064
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | tert-Butyl (5-bromopyridin-3-yl)carbamate | HCID 11403050 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamate | HCID 89546780 | 37.9% |
Reaction Steps
Cesium carbonate (214 mg), pyrrole (30 mg), Xantphos (63 mg), and Pd2(dba)3 (50 mg) were added to a 1,4-dioxane solution (5 mL) containing tert-butyl(5-bromopyridin-3-yl)carbamate (100 mg) in a nitrogen atmosphere, followed by stirring at 100° C. for 8 hours. The reaction solution was adjusted to room temperature, and water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. Then, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=5:1 to 1:1), and a light yellow solid of tert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamate (36 mg) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772320B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-bccea73b09e84279a18652a6f40b0e2f |
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| Source note | uspto-grants-2014_07 |
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