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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373644Generated: October 25, 2026

Diisopropylethylamine → N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamide

https://huagongshe.com/reaction/2373644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57444358HCID 57444358—
Reactant2-{3-[(Methylsulfonyl)amino]phenyl}ethyl methanesulfonateHCID 57444359—
SolventDimethylformamideHCID 6228—
ProductN-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamideHCID 5744435737.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-methyl-5-(1-piperazinyl)quinazoline (50 mg), 2-{3-[(methylsulfonyl)amino]phenyl}ethyl methanesulfonate (65 mg), diisopropylethylamine (192 μL) and DMF (0.5 mL) was heated to 100° C. in a sealed tube and stirred for 24 hours. The mixture was cooled to room temperature and partitioned between aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed (water, brine), dried (sodium sulfate) and concentrated in vacuo. The residue was purified by column chromatography [SiO2; DCM-MeOH: (100:0)→(95:5)] to give the title compound as a beige foam (35 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459456B2
Source datasetuspto-grants-2008_12
ORD IDord-244d5e038dd94076baad4e85bf3aa668
Source noteuspto-grants-2008_12