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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406712Generated: November 1, 2026

Pyrrole → tert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamate

https://huagongshe.com/reaction/2406712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrroleHCID 8027—
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactanttert-Butyl (5-bromopyridin-3-yl)carbamateHCID 11403050—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamateHCID 8954678037.9%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809371B2
Source datasetuspto-grants-2014_08
ORD IDord-7d2f8fcac6524557a60ea91e20bafac0
Source noteuspto-grants-2014_08