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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748567Generated: October 31, 2026

Cesium carbonate → 1-(5-Acetylpyridin-2-yl)pyrrole-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1748567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttert-butyl 1H-pyrrole-3-carboxylateHCID 11171190—
Reactant5-Acetyl-2-bromopyridineHCID 15668195—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventTolueneHCID 1140—
Product1-(5-Acetylpyridin-2-yl)pyrrole-3-carboxylic acid tert-butyl esterHCID 8669251331.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 1H-pyrrole-3-carboxylic acid tert-butyl ester (700 mg) described in Reference Example 50, 1,1′-bis(diphenylphosphino)ferrocene (35 mg), palladium acetate (9.4 mg), cesium carbonate (1.64 g) and 5-acetyl-2-bromopyridine (921 mg) in toluene (10 ml) was stirred at 100° C. for 8 hours. After completion of the reaction, the mixture was allowed to cool to room temperature, ice water was added thereto, and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated in vacuo. The obtained residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give 1-(5-acetylpyridin-2-yl)pyrrole-3-carboxylic acid tert-butyl ester (380 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-d1ca1a8a6f3549d399ab335850cd181f
Source noteuspto-grants-2015_10