Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624103Generated: October 31, 2026

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

https://huagongshe.com/reaction/624103

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 mmol), potassium carbonate (109 mg, 789 mmol) and potassium iodide (53 mg, 319 mmol) 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 numberUS09303026B2
Source datasetuspto-grants-2016_04
ORD IDord-2df3f614c09b44bbb766e9594385b2f0
Source noteuspto-grants-2016_04