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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502478Generated: November 1, 2026

Sodium Carbonate → Tert-butyl 7-(4-methylpyridin-3-yl)-2,6-naphthyridin-3-ylcarbamate

https://huagongshe.com/reaction/1502478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Methylpyridine-3-Boronic AcidHCID 2762711—
ReactantTert-butyl 7-chloro-2,6-naphthyridin-3-ylcarbamateHCID 86674971—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 7-(4-methylpyridin-3-yl)-2,6-naphthyridin-3-ylcarbamateHCID 7111514034.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of tert-butyl N-(7-chloro-2,6-naphthyridin-3-yl)carbamate (460 mg, 1.65 mmol), (4-methyl-3-pyridyl)boronic acid (450 mg, 3.3 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (117 mg, 0.165 mmol) and saturated aqueous sodium carbonate solution (0.5 mL) in acetonitrile (5 mL) was heated under microwave irradiation (Biotage) at 130° C. for 30 minutes. The reaction mixture was diluted with ethyl acetate (150 mL) and washed with water (50 mL). The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to provide a residue that was purified by flash chromatography (12 g, Silica, 0-10% methanol in dichloromethane). Desired fractions were combined and evaporated in vacuo to afford the title compound as a white solid (190 mg, 34%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-a1ee3abfcf23401fb584c4e02c7a1132
Source noteuspto-grants-2015_12