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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914947Generated: October 31, 2026

Sodium Bicarbonate → HCID 53344959, compound

https://huagongshe.com/reaction/1914947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53344730HCID 53344730—
Reactant3-bromo-5-[1-(2-pyrrolidin-1-yl-ethyl)-1H-pyrazol-4-yl]-pyridineHCID 67364972—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53344959HCID 53344959—

Reaction Conditions

Temperature80 °C

Reaction Steps

A slurry of 161 mg (0.50 mmol) 3-bromo-5-[1-(2-pyrrolidin-1-yl-ethyl)-1H-pyrazol-4-yl]-pyridine, 167 mg (0.55 mmol) 2-(5-Chloro-2-fluoro-phenyl)-[1,8]naphthyridine-4-boronic acid and 50.4 mg (0.6 mmol) sodium bicarbonate in 2 ml DMF and 0.5 ml water was heated at 80° C. under nitrogen. Then 7.0 mg (0.01 mmol) bis-(triphenylphosphine)-palladium(II)-chloride were added. The reaction mixture was stirred for 40 hours at 80° C. Water was added, the resulting precipitate was filtered off and washed with water. The residue was chromatographed on a silica gel column with dichloromethane/methanol as eluent yielding 2-(5-Chloro-2-fluoro-phenyl)-4-{5-[1-(2-pyrrolidin-1-yl-ethyl)-1H-pyrazol-4-yl]-pyridin-3-yl}-[1,8]naphthyridine as colourless crystals; HPLC-MS: 1.67 min, [M+H] 499.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614226B2
Source datasetuspto-grants-2013_12
ORD IDord-299a6f068b3c42c985137ef53c4efc33
Source noteuspto-grants-2013_12