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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920004Generated: October 29, 2026

Hydrochloric Acid → HCID 68297341, compound

https://huagongshe.com/reaction/920004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant3-(Tributylstannyl)pyridineHCID 3483848—
ReactantHCID 86714167HCID 86714167—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68297341HCID 6829734140.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 8-bromo-5-hydroxy-2-oxo-3-phenyl-1-(tetrahydro-pyran-4-ylmethyl)-1,2-dihydro-[1,7]naphthyridine-6-carboxylic acid methyl ester (91 mg, 0.19 mmol), 3-tributylstannanyl-pyridine (0.092 mL, 0.29 mmol) and PdCl2(PPh3)2 (27 mg, 0.038 mmol) in 4 mL of DMF was heated at 120° C. for 3 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 (10-100% EtOAc/hexanes+1% AcOH) and preparative TLC (5% MeOH/CH2Cl2) to give 36 mg of the title compound. MS: (+) m/z 472.41 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09271970B2
Source datasetuspto-grants-2016_03
ORD IDord-f8c01e817a624c4ebede5a88cb7dc98f
Source noteuspto-grants-2016_03