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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476181Generated: November 2, 2026

Dichloromethane → HCID 178489150, compound

https://huagongshe.com/reaction/1476181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant3,4-Dimethoxyphenylboronic acidHCID 2734702—
ReactantHCID 178508725HCID 178508725—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178489150HCID 17848915021.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (1.00 g, 3.83 mmoles) in DMF (10 ml), ethanol (5 ml) and water (5 ml), 3,4-dimethoxyphenyl boronic acid (1.04 g, 5.746 mmoles) and sodium carbonate (2.03 g, 19.15 mmoles) were added and the system is degassed for 30 min Tetrakis triphenylphosphine Palladium (0.872 g, 0.754 mmoles) was added under nitrogen atmosphere and heated to 80° C. After 12 h, the reaction mixture was celite filtered, concentrated and extracted with ethyl acetate. The organic layer was dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol:dichloromethane to afford the title compound as yellow solid (0.220 g, 21% yield). 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 13.46(s, 1H), 8.19(s, 1H), 7.20(s,1H), 7.19(d, J=9.3Hz, 1H), 7.11(d, J=8.1Hz 1H), 3.81(s,6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018375B2
Source datasetuspto-grants-2015_04
ORD IDord-1afe7100e6d4446ab5949ad375ce801a
Source noteuspto-grants-2015_04