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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371482Generated: November 1, 2026

Potassium Iodide → HCID 10142294, compound

https://huagongshe.com/reaction/1371482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21935995HCID 21935995—
SolventDimethylformamideHCID 6228—
ProductHCID 10142294HCID 10142294—

Reaction Steps

A mixture of 4-(6-chloro-2,3-methylenedioxyanilino)-6-methoxy-7-(3-piperazin-1-ylpropoxy)quinazoline (0.19 g), 2-chloroacetonitrile (0.038 ml), potassium iodide (0.020 g), potassium carbonate (0.139 g) and DMF (2.5 ml) was stirred at ambient temperature for 16 hours. The reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water and with brine, dried over magnesium sulphate and evaporated. The crude product was purified by column chromatography on silica using a 93:7 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound (0.13 g) as a solid; NMR Spectrum: (DMSOd6 and CF3CO2D) 2.3 (m, 2H), 2.6 (m, 2H), 3.05 (m, 2H), 3.15 (m, 2H), 3.35 (m, 2H), 3.65 (m, 2H), 3.9 (s, 2H), 4.05 (s, 3H), 4.35 (m, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.15 (d, 1H), 7.4 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: [M−H]− 509 and 511; Elemental Analysis: Found C, 58.41; H, 5.62; N, 15.93. C25H27ClN6O40.2H2O requires C, 58.35; H. 5.37; N, 16.33%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157467B2
Source datasetuspto-grants-2007_01
ORD IDord-9099b02ac9af486983d523265ca2d607
Source noteuspto-grants-2007_01