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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192966Generated: November 1, 2026

Sodium Carbonate → HCID 178450361, compound

https://huagongshe.com/reaction/2192966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium ChlorideHCID 433294—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantHCID 178450360HCID 178450360—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178450361HCID 178450361—

Reaction Conditions

Temperature135 °C

Reaction Steps

To a mixture of 9-bromo-1-butoxybenzo[c]-1,6-naphthyridin-6-ol (251 mg, 0.723 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (256 mg, 1.229 mmol), lithium chloride (184 mg, 4.34 mmol), and tetrakis(triphenylphosphine)palladium (251 mg, 0.217 mmol) in DMF (7229 μl) in a sealed tube, sodium carbonate (3615 μl, 7.23 mmol, 2 M) was added, and the reaction mixture was heated to 135° C. After 2 h, the reaction mixture was allowed to cool to room temperature and poured into water. This mixture was then filtered through a frit. The filter cake was washed with dichloromethane. The filter cake was then collected and dried under high vacuum to afford 1-butoxy-9-(1-methyl-1H-pyrazol-4-yl)benzo[c]-1,6-naphthyridin-6-ol as a white solid. LRMS (APCI) calc'd for (C20H21N4O2) [M+H]+, 349.2; found 349.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329722B2
Source datasetuspto-grants-2012_12
ORD IDord-73cdb01bd53b4bcf8ee2ca601a8d5924
Source noteuspto-grants-2012_12