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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239682Generated: October 28, 2026

Dichloromethane → HCID 178434217, compound

https://huagongshe.com/reaction/239682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 53234609HCID 53234609—
Reactant2-(1-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-3-(3-fluorophenyl)-4H-chromen-4-oneHCID 66579932—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178434217HCID 17843421720.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of Example 57c (0.477 g, 0.930 mmoles) in DMF (5.3 ml), ethanol (2.6 ml) and water (2.6 ml), N-Boc-3-methyl-6-indazoleboronic acid pinacol ester 98 (0.500 g, 1.395 mmoles) and sodium carbonate (0.295 g, 3.318 mmoles) were added and the system is degassed for 30 min. Tetrakistriphenylphosphine Palladium (0.053 g, 0.046 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 (0.100 g, 20% yield). MP: 246-248° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 12.75(s,1H), 8.22(s,1H), 8.06(dd, J=8.5,1.8 Hz, 1H), 7.84(d, J=8.3 Hz, 1H), 7.80(m,1H), 7.62(s,1H), 7.51(d, J=8.2 Hz, 2H), 7.39-7.31(m, 2H), 7.18(m, 2H), 7.12(dt, J=8.3,2.6 Hz, 1H), 5.56(s,2H), 2.51(s,3H). Mass: 517.51(M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642607B2
Source datasetuspto-grants-2014_02
ORD IDord-5a2318d23ffe4d32b0bce67bc07992f8
Source noteuspto-grants-2014_02