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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712593Generated: October 29, 2026

Potassium Carbonate → HCID 117667315, compound

https://huagongshe.com/reaction/712593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant6-Bromo-1,2,3,4-tetrahydro-1,8-naphthyridineHCID 17930126—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 117667315HCID 11766731561.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

6-Bromo-1,2,3,4-tetrahydro-[1,8]naphthyridine (243 mg, 1.1 mmol), 3-pyridinyl-boronic acid (168 mg, 1.4 mmol) and K2CO3 (315 mg, 2.3 mmol) are mixed in 3.0 mL of 1,4-dioxane and 0.30 mL of water. Argon gas is bubbled through the mixture for 10 min and bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) (81 mg, 0.11 mmol) is added. The mixture is heated at 100° C. for 16 hrs. Then solvents are removed and EtOAc (50 mL) is added along with 30 mL of water. The mixture is filtered to remove any solid and the organic layer is separated. The aqueous layer is extracted with EtOAc (2×25 mL) and the organic layers are combined and concentrated to give the crude product. Purification by flash column chromatography affords 143 mg of 6-Pyridin-3-yl-1,2,3,4-tetrahydro-[1,8]naphthyridine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-51b3c018303248b78976cd987a8ea1ac
Source noteuspto-grants-2015_11