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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354199Generated: October 31, 2026

Sodium Iodide → HCID 11384223, compound

https://huagongshe.com/reaction/2354199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 11404895HCID 11404895—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
SolventAcetoneHCID 180—
ProductHCID 11384223HCID 1138422387.5%

Reaction Steps

N-Cyclopropyl-3-(6-hydroxy-4-oxoquinazolin-3 (4H)-yl)-4-methylbenzamide (0.15 g), 2-dimethylaminoethyl chloride hydrochloride (0.084 g), potassium carbonate (0.62 g), and sodium iodide (0.007 g) were stirred in acetone (9 ml) at 60° C. for 18 hours. The reaction mixture was filtered, the solids washed with acetone, and the filtrate was concentrated. The residue was dissolved in ethyl acetate and washed with 2N NaOH solution, brine, dried (magnesium sulfate) and concentrated. Purification by column chromatography on a silica column eluting with 10% methanol/ethyl acetate+1% aqueous ammonia solution gave the title compound (0.159 g) as a white solid; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.70 (m, 2H), 2.13 (s, 3H), 2.23 (s, 6H), 2.68 (t, 2H), 2.85 (m, 1H), 4.19 (t, 2H), 7.52 (m, 2H), 7.60 (s, 1H), 7.72 (d, 1H), 7.83 (s, 1H), 7.91 (d, 1H), 8.19 (s, 1H), 8.42 (d, 1H); Mass Spectrum: M+H+ 407.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-bd9397144368450583c3ee88350daeee
Source noteuspto-grants-2010_07