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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879953Generated: November 3, 2026

Potassium Iodide → HCID 86619731, compound

https://huagongshe.com/reaction/1879953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl chloroacetateHCID 66052—
ReactantN-(3-chloro-2-fluorophenyl)-7-methoxy-6-(piperidin-4-yloxy)quinazolin-4-amineHCID 10408840—
SolventDimethylacetamideHCID 31374—
ProductHCID 86619731HCID 8661973160%

Reaction Conditions

Temperature70 °C

Reaction Steps

Tert-butyl chloroacetate (1.43 ml, 10 mmol) was added dropwise to a mixture of 4-(3-chloro-2-fluoroanilino)-7-methoxy-6-[(piperidin-4-yl)oxy]quinazoline (4.02 g, 10 mmol), potassium iodide (1.66 g, 10 mmol) and potassium carbonate (1.66 g, 12 mmol) in dimethylacetamide (50 ml). The mixture was heated at 70° C. for one hour. After evaporation of the solvents under vacuum, the residue was triturated in water. The resulting solid was filtered, washed with water and purified by chromatography on silica gel (eluant: 2% 7N methanolic ammonia in dichloromethane) to give tert-butyl[4-({4-(3-chloro-2-fluoroanilino)-7-methoxyquinazolin-6-yl}oxy)piperidin-1-yl]acetate as a white solid (3.0 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318752B2
Source datasetuspto-grants-2012_11
ORD IDord-58f4e3beefda40c09d41b8f1e6f73a5e
Source noteuspto-grants-2012_11