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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411091Generated: October 31, 2026

Hydrochloric Acid → HCID 68297209, compound

https://huagongshe.com/reaction/1411091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantTributylphenyltinHCID 607632—
ReactantHCID 68297220HCID 68297220—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68297209HCID 6829720956.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-bromo-1-(2-ethyl-butyl)-5-hydroxy-2-oxo-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (500 mg, 1.3 mmol), PhSnBu3 (0.51 mL, 1.6 mmol), and PdCl2(PPh3)2 (183 mg, 0.26 mmol) in DMF (25 mL) was heated at 120° C. under nitrogen atmosphere for 3 h. After the mixture was cooled to r.t., brine and EtOAc were added. 1 M HCl was added until pH was about 3. The aqueous layer was extracted with additional EtOAc and the organic layers were combined, washed with water and brine, and dried over MgSO4. After evaporating the solvent in vacuo, the crude product was chromatographed (3-35% EtOAc/hexanes+1% AcOH) to give 280 mg of the title compound as a yellow solid. MS: (+) m/z 381.34 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921389B2
Source datasetuspto-grants-2014_12
ORD IDord-d229ec59df95430aa6f78cedf38ca6fb
Source noteuspto-grants-2014_12