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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371480Generated: November 1, 2026

Sodium Iodide → HCID 21936071, compound

https://huagongshe.com/reaction/1371480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantHCID 21936037HCID 21936037—
SolventAcetonitrileHCID 6342—
ProductHCID 21936071HCID 21936071—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 7-(2-bromoethoxy)-4-(2,3-methylenedioxyanilino)-6-methoxyquinazoline (0.48 g) homopiperidine (0.322 ml), sodium iodide (0.002 g), DMF (5 ml) and acetonitrile (6 ml) was stirred and heated to 45° C. for 5 hours. The mixture was evaporated and the residue was partitioned between methylene chloride 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 19:1 mixture of methylene chloride and a saturated methanolic ammonia solution as eluent. The material so obtained was triturated under diethyl ether to give the title compound as a solid (0.4 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 1.65 (m, 4H), 1.9 (m, 4H), 3.35 (m, 2H), 3.55 (m, 2H), 3.7 (m, 2H), 4.0 (s, 3H), 4.6 (m, 2H), 6.1 (s, 2H), 7.0 (m, 3H), 7.45 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: M+H+ 437.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157467B2
Source datasetuspto-grants-2007_01
ORD IDord-702ac0bd3b854bae95788684a2a9a3c5
Source noteuspto-grants-2007_01