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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476238Generated: October 26, 2026

Dichloromethane → HCID 178434219, compound

https://huagongshe.com/reaction/1476238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant2-(1-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-3-phenyl-4H-chromen-4-oneHCID 58269110—
Reactant3-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1H-indazoleHCID 178434208—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178434219HCID 17843421921%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of Example 57b (0.350 g, 0.684 mmoles) in DMF (3.5 ml), ethanol (1.7 ml) and water (1.7 ml), 3-methyl-6-indazoleboronic acid pinacol ester 97 (0.353 g, 1.369 mmoles) and sodium carbonate (0.217 g, 2.05 mmoles) were added and the system is degassed for 30 min Tetrakistriphenylphosphine Palladium (0.040 g, 0.034 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 brown solid (0.073 g, 21% yield). MP: 249-252° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 12.75(s,1H), 8.09(s,1H), 8.05(dd, J=8.0,1.6 Hz, 1H), 7.85(d, J=8.2 Hz, 1H), 7.81(m,1H), 7.64(s,1H), 7.62(d, J=8.4 Hz, 1H), 7.51(t, J=7.3 Hz, 1H), 7.36(dd, J=9.3,1.0 Hz, 1H), 7.29(m,3H), 7.15(br s,2H), 6.01(q, J=7.0 Hz, 1H), 2.52(s,3H), 1.92(d, J=7.0 Hz, 3H). Mass: 514.18(M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018375B2
Source datasetuspto-grants-2015_04
ORD IDord-8b90d08b6bd5489db65723daf7d9e438
Source noteuspto-grants-2015_04