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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388124Generated: October 29, 2026

Potassium Carbonate → HCID 66699704, compound

https://huagongshe.com/reaction/388124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantQuinolin-5-ylboronic acidHCID 5153389—
ReactantHCID 66699880HCID 66699880—
ReactantHCID 86626406HCID 86626406—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66699704HCID 6669970474%

Reaction Conditions

Temperature85 °C

Reaction Steps

(R)-3-Nitro-N-(1-phenylethyl)-6-(quinolin-5-yl)pyridin-2-amine. To a solution of (R)-6-chloro-3-nitro-N-(1-phenylethyl)pyridin-2-amine (1.12 g, 4.03 mmol) and quinolin-5-ylboronic acid (0.91 g, 5.24 mmol) in DMF (75 mL) was added potassium carbonate (2.23 g, 16.1 mmol) in water (25 mL). The reaction solution was purged with a stream of nitrogen followed by the addition of tetrakis(triphenylphosphine)palladium(0) (0.466 g, 0.403 mmol). After heating at 85° C. for 2 h, the solvent was removed under reduced pressure. The crude product was purified by silica gel chromatography to afford the title compound (1.1 g, 74% yield). MS (ESI) m/z 371.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372976B2
Source datasetuspto-grants-2013_02
ORD IDord-2acd5c9d6cc840f5882186cf971285e2
Source noteuspto-grants-2013_02