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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410959Generated: November 1, 2026

Hydrochloric Acid → HCID 68297503, compound

https://huagongshe.com/reaction/1410959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant3-(Tributylstannyl)pyridineHCID 3483848—
ReactantHCID 86714158HCID 86714158—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68297503HCID 6829750348.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 8-bromo-5-hydroxy-1-methyl-2-oxo-3-phenyl-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (69 mg, 0.18 mmol), 3-tributylstannanyl-pyridine (0.085 mL, 0.27 mmol) and PdCl2(PPh3)2 (25 mg, 0.035 mmol) in 3 mL of DMF was heated at 120° C. for 2 h under nitrogen atmosphere. After the mixture was cooled to r.t., EtOAc and brine were added. 1 M HCl was added with stirring until pH was about 3-4. The aqueous layer was extracted with additional EtOAc, and the combined organic layer was washed with water and dried over MgSO4. After evaporating the solvent in vacuo, the crude product was purified sequentially by flash chromatography (15-100% EtOAc/hexanes+1% AcOH), preparative TLC (5% MeOH/CH2Cl2), and flash chromatography (0-2% MeOH/CH2Cl2) to give 34 mg of the title compound. MS: (+) m/z 388.39 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921389B2
Source datasetuspto-grants-2014_12
ORD IDord-e9ffde08d5224e0a95a1dcf1a8d4197d
Source noteuspto-grants-2014_12