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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476178Generated: October 30, 2026

Dichloromethane → HCID 178492925, compound

https://huagongshe.com/reaction/1476178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant(4-Fluoro-2-methoxyphenyl)boronic acidHCID 2782672—
ReactantHCID 178508725HCID 178508725—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178492925HCID 17849292535.3%

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 (14 ml), ethanol (7 ml) and water (7 ml), 4-fluoro-2-methoxyphenyl boronic acid (0.846 g, 4.979 mmoles) and sodium carbonate (2.06 g, 19.15 mmoles) were added and the system is degassed for 30 min Tetrakis triphenylphosphine Palladium (0.754 g, 0.652 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 off-white solid (0.350 g, 35% yield). 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 13.46(s, 1H), 8.14(s, 1H), 7.40(t, J=8.4Hz, 1H), 7.09(dd, J=11.5,2.9Hz, 1H),6.91(dt, J=8.4,2.4Hz 1H),3.78(s,3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018375B2
Source datasetuspto-grants-2015_04
ORD IDord-1b10bd7b4815498f9b3c6a30088b5daa
Source noteuspto-grants-2015_04