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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468556Generated: October 29, 2026

Potassium Iodide → 4-Ethoxy-7-[2-[1-(6-methylpyridazin-3-yl)-4-piperidyl]ethoxy]quinazoline

https://huagongshe.com/reaction/468556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[4-(2-Chloroethyl)-1-piperidinyl]-6-methylpyridazineHCID 14989218—
Reactant7-Hydroxy-4-ethoxyquinazolineHCID 135848747—
SolventDimethylformamideHCID 6228—
Product4-Ethoxy-7-[2-[1-(6-methylpyridazin-3-yl)-4-piperidyl]ethoxy]quinazolineHCID 50447018%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-[4-(2-chloroethyl)-1-piperidinyl]-6-methyl pyridazine (76 mg, 318 μmol), 7-hydroxy-4-ethoxyquinazoline (100 mg, 526 μmol), potassium carbonate (109 mg, 789 μmol) and potassium iodide (53 mg, 319 μmol) in DMF (5 mL) was heated at 90° C. overnight in an argon atmosphere. The mixture was concentrated, and the residue partitioned between ethyl acetate (100 mL), and water (20 mL). The organic phase was dried (MgSO4), filtered, concentrated and purified by column chromatography (silica), using gradient elution (ethyl acetate-methanol/EA). The combined fractions gave a white solid (22 mg, 18%). The 1H nmr data are recorded in Table 6 below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624025B2
Source datasetuspto-grants-2014_01
ORD IDord-108ac16d688549d381a0e4efadef53ce
Source noteuspto-grants-2014_01