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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239694Generated: October 28, 2026

Dichloromethane → HCID 53235316, compound

https://huagongshe.com/reaction/239694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant3-methyl-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indoleHCID 53234611—
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 53235316HCID 5323531610%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of Example 57c (0.400 g, 0.758 mmoles) in DMF (4 ml), ethanol (2 ml) and water (2 ml), 3-methyl-6-indoleboronic acid pinacol ester 106 (0.390 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 (0.043 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 off-white solid (0.040 g, 10% yield). MP: 269-272° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 10.91(s,1H), 8.06(s,1H), 8.05(d, J=7.8 Hz, 1H),7.85(t, J=7.2 Hz, 1H),7.68(d, J=8.4 Hz, 1H),7.63(d, J=7.1 Hz, 1H),7.56(s,1H), 7.53(t, J=7.8 Hz, 1H),7.25(d, J=8.1 Hz, 1H),7.28(br s,1H), 7.21(s,1H), 7.06(dt, J=9.0,2.8 Hz, 1H), 6.98(br s,2H), 6.04(q, J=7.0 Hz, 1H),2.28(s,3H),1.91(d, J=7.0 Hz, 3H). Mass: 530.99(M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642607B2
Source datasetuspto-grants-2014_02
ORD IDord-d1757721e2e94871a5fae1a0e6c4d89f
Source noteuspto-grants-2014_02