戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2373644作成日:2026年10月26日

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

https://huagongshe.com/reaction/2373644

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2-Methyl-5-(1-piperazinyl)quinazolineHCID 57444358—
反応物2-{3-[(Methylsulfonyl)amino]phenyl}ethyl methanesulfonateHCID 57444359—
溶媒DimethylformamideHCID 6228—
生成物N-(3-{2-[4-(2-methyl-5-quinazolinyl)-1-piperazinyl]ethyl}phenyl)methanesulfonamideHCID 5744435737.6%

反応条件

温度100 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07459456B2
出典データセットuspto-grants-2008_12
ORD IDord-244d5e038dd94076baad4e85bf3aa668
出典メモuspto-grants-2008_12