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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927518Generated: October 27, 2026

Hydrochloric Acid → 6-(3-Chloro-phenyl)-5-cyclopentyl-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/927518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant6-Bromo-5-cyclopentyl-pyridine-2-carboxylic acid methyl esterHCID 86674764—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-(3-Chloro-phenyl)-5-cyclopentyl-pyridine-2-carboxylic acidHCID 7108755220.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

6-Bromo-5-cyclopentyl-pyridine-2-carboxylic acid methyl ester (0.6 g, 2.1 mmol), bis(diphenylphosphino)ferrocene-palladium(II)dichloride methylene chloride complex (CAN 95464-05-4, 90 mg, 0.11 mmol) and potassium carbonate (0.37 g, 2.68 mmol) were added to a solution of 3-chlorophenylboronic acid (CAN 63503-60-6, 0.42 g, 2.69 mmol) in water (20 mL) and DMF (2 mL). The mixture was stirred for 48 h at 100° C. Its pH was adjusted to pH=3 with diluted hydrochloric acid. The mixture was extracted with methylene chloride (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure to give the title compound (130 mg, 20%) which was used in the next step without further purification; MS (EI): m/e=302.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290451B2
Source datasetuspto-grants-2016_03
ORD IDord-f5a7280693d34bc1a0fda956581c009c
Source noteuspto-grants-2016_03