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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15872Generated: October 25, 2026

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

https://huagongshe.com/reaction/15872

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 numberUS07732600B2
Source datasetuspto-grants-2010_06
ORD IDord-54de705710c246bd894c0bfe20ad94e2
Source noteuspto-grants-2010_06