Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239688Generated: October 29, 2026

Dichloromethane → HCID 178434221, compound

https://huagongshe.com/reaction/239688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant2-(1-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-6-fluoro-3-phenyl-4H-chromen-4-oneHCID 58269264—
Reactant3-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1H-indazoleHCID 178434208—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178434221HCID 17843422116.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of Example 57e (0.400 g, 0.758 mmoles) in DMF (4 ml), ethanol (2 ml) and water (2 ml), 3-methyl-6-indazoleboronic acid pinacol ester 97 (0.391 g, 1.517 mmoles) and sodium carbonate (0.241 g, 2.27 mmoles) were added and the system is degassed for 30 min. Tetrakistriphenylphosphine Palladium (0.044 g, 0.037 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 (0.065 g, 15% yield). MP: 253-255° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 12.75(s,1H), 8.08(s,1H), 7.85(d, J=8.3 Hz, 1H), 7.75(m,3H), 7.63(s,1H), 7.35(dd, J=8.4,1.2 Hz, 1H), 7.28(m,3H), 7.14(br s,2H), 6.00(q, J=7.1 Hz, 1H),2.52(s,3H), 1.91(d, J=7.1 Hz, 3H). Mass: 532.03(M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642607B2
Source datasetuspto-grants-2014_02
ORD IDord-c3cdda91b0d8408f83bf398eb5ebd401
Source noteuspto-grants-2014_02