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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826317Generated: October 31, 2026

Sodium Iodide → HCID 22140831, compound

https://huagongshe.com/reaction/1826317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22140783HCID 22140783—
SolventDimethylformamideHCID 6228—
ProductHCID 22140831HCID 22140831—

Reaction Steps

A mixture of 4-(6-chloro-2,3-methylenedioxyanilino)-7-(3-piperazin-1-ylpropoxy)-5-tetrahydropyran-4-yloxyquinazoline (1.3 g), 2-chloroacetonitrile (0.167 ml), sodium iodide (0.036 g), potassium carbonate (0.331 g) and DMF (15 ml) was stirred at ambient temperature for 5 hours. The mixture was evaporated and the residue was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using a 10:9:1 mixture of ethyl acetate, methylene chloride and methanol as eluent. There was thus obtained the title compound (0.69 g); NMR Spectrum: (CDCl3) 1.85–2.0 (m, 4H), 2.1 (m, 2H), 2.4–2.5 (m, 6H), 2.5–2.6 (m, 4H), 3.42 (s, 2H), 3.5–3.6 (m, 2H), 3.9–4.0 (m, 2H), 4.0–4.1 (m, 2H), 4.7 (m, 1H), 6.0 (s, 2H), 6.42 (s, 1H), 6.65 (d, 1H), 6.78 (d, 1H), 6.9 (d, 1H), 8.42 (s, 1H), 9.2 (s, 1H ); Mass Spectrum: M+H+ 581 and 583.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049438B2
Source datasetuspto-grants-2006_05
ORD IDord-9fa2d420f7214bbb8f1cf02a72ca23ca
Source noteuspto-grants-2006_05