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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712692Generated: October 30, 2026

Sodium Carbonate → HCID 117667664, compound

https://huagongshe.com/reaction/712692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant1432621-15-2HCID 75406685—
ReactantHCID 117667602HCID 117667602—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 117667664HCID 1176676646.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A vial containing 6-bromo-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide (350 mg, 1.4 mmol), bis(pinacolato)diboron (573 mg, 2.3 mmol), 1,1′-bis(diphenylphosphino)ferrocenedichloropalladium (II) (50 mg, 0.068 mmol) and potassium acetate (604 mg, 6.2 mmol) in 1,4-dioxane (10 mL) is flushed with Ar, sealed tightly and heated to 80° C. for 2 h. The reaction mixture is cooled to room temperature and a solution of 3-(5-bromo-pyridin-3-yl)-oxetan-3-ol (314 mg, 1.37 mmol) in 1,4-dioxane (4 mL), aqueous sodium carbonate solution (2M, 1.4 mL, 2.7 mmol) and additional 1,1′-bis(diphenylphosphino)ferrocenedichloropalladium (II) (50 mg, 0.068 mmol) are added. The mixture is flushed with Ar, sealed tightly and heated to 100° C. for 90 min. After cooling to room temperature the mixture is partitioned between water and EtOAc. The layers are separated and the aqueous is further extracted with EtOAc. The combined organic layers are washed with brine, dried (Na2SO4) and concentrated. To the residue is added MeOH to form a precipitate which is collected by filtration to afford the title compound (28 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-2fc45fcae2334ecd9384057d737bd04c
Source noteuspto-grants-2015_11