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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513312Generated: November 3, 2026

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

https://huagongshe.com/reaction/1513312

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-methylpyridazine (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 numberUS08217171B2
Source datasetuspto-grants-2012_07
ORD IDord-d69aa4a982214c9395d0f00624ff823f
Source noteuspto-grants-2012_07