Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766437Generated: October 30, 2026

Triethylamine → 5-(2-Chloro-5-trifluoromethyl-phenyl)-6-cyclopentyloxy-3-pyridinecarboxylic acid methyl ester

https://huagongshe.com/reaction/1766437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Chloro-5-(trifluoromethyl)phenylboronic acidHCID 2782670—
ReactantMethyl 5-bromo-6-(cyclopentyloxy)nicotinateHCID 66844699—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product5-(2-Chloro-5-trifluoromethyl-phenyl)-6-cyclopentyloxy-3-pyridinecarboxylic acid methyl esterHCID 6750535461.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-Bromo-6-cyclopentyloxy-3-pyridinecarboxylic acid methyl ester (0.33 g, 1.1 mmol) was dissolved in DMF (3.5 mL). To this solution was added [2-chloro-5-(trifluoromethyl)phenyl]-boronic acid (370 mg, 1.6 mmol), palladium(II)acetate (7 mg), triphenylphosphine (18 mg) and triethylamine (0.46 mL). The whole mixture was heated with stirring at 100° C. for 20 h, cooled to room temperature and partitioned between dichloromethane and a mixture of water and concentrated ammonium hydroxide solution (water/ammonia 4:1 v/v). Organic phases were pooled, dried with MgSO4 and the solvent was evaporated. The residue was purified by column chromatography on silica (n-heptane/ethyl acetate 6:1) to yield 0.27 g of the title compound as a light yellow oil, MS (ISP) 400.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229999B2
Source datasetuspto-grants-2007_06
ORD IDord-8864d714172d4e75aa8ca8661ecfd70a
Source noteuspto-grants-2007_06