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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748488Generated: October 29, 2026

Potassium Phosphate, Tribasic → 1-(5-Ethylpyridin-2-yl)pyrrole-3-carboxylic acid

https://huagongshe.com/reaction/1748488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant1-(5-Chloropyridin-2-yl)pyrrole-3-carboxylic acid tert-butyl esterHCID 86692447—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product1-(5-Ethylpyridin-2-yl)pyrrole-3-carboxylic acidHCID 86692449197.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

Tetrehydrofuran (7.2 ml) was added to 1-(5-chloropyridin-2-yl)pyrrole-3-carboxylic acid tert-butyl ester (1.0 g) described in Reference Example 55(1), palladium (II) acetate (80 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (S-Phos) (147 mg), vinylboronic acid pinacol ester (860 μl) and tripotassium phosphate (1.9 g) and stirred at 100° C. for 8.5 hours. Water was added to the reaction solution and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo. 1,4-Dioxane (15 ml) and 10% palladium-carbon (containing ca. 50% water; 200 mg) was added to the resulting residue and the mixture was stirred under hydrogen atmosphere at room temperature for six hours. The reaction solution was filtered through Celite and the filtrate was concentrated in vacuo. The residue was purified with silica gel column chromatography (n-hexane/ethyl acetate). To the resulting residue was added Dichloromethane (10 ml) and trifluoroacetic acid (3 ml) and the mixture was stirred at room temperature for 4.5 hours. Water was added to the reaction solution and the precipitated solid was washed with water. The resulting solid was dissolved in ethyl acetate, extracted with 4N aqueous solution of sodium hydroxide and the aqueous layer was acidified by the addition of 1N hydrochloric acid aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo to give the titled compound (153 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-08fe1d53f9b04e339e6ae3b004df70af
Source noteuspto-grants-2015_10