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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811909Generated: October 26, 2026

2-Chloroquinoline-3-boronic acid → 2-Chloro-3-(2-methyl-9-(tetrahydro-2H-pyran-2-YL)-9H-purin-6-YL)quinoline

https://huagongshe.com/reaction/1811909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroquinoline-3-boronic acidHCID 4198643—
Reactant6-chloro-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 59548268—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-3-(2-methyl-9-(tetrahydro-2H-pyran-2-YL)-9H-purin-6-YL)quinolineHCID 86647052—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 6-chloro-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (0.55 g, 2.18 mmol), 2-chloroquinolin-3-ylboronic acid (0.90 g, 4.35 mmol, Aldrich, St. Louis, Mo.) and tetrakis(triphenylphosphine)palladium(0) (0.13 g, 0.11 mmol, Strem Chemicals, Inc., Newburyport, Mass.) in dioxane (3 mL) and water (1 mL) was sealed and purged with argon for several minutes. The reaction mixture was stirred at 90° C. for 6 h and then allowed to cool to room temperature. The organic phase was taken and the solvents removed under vacuum. Purification of the crude reaction mixture by silica gel chromatography (0 to 3% MeOH/CH2Cl2) provided the title compound as an orange solid. m/z (ESI, +ve ion) 380 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-e6bf2c1d28ed41ac871beb8d9c2a5375
Source noteuspto-grants-2013_01