戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6181作成日:2026年10月25日

Water → 3-[3-(4-pyridylthio)propyl]quinazoline-2,4(1H,3H)-dione

https://huagongshe.com/reaction/6181

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物QuinazolinedioneHCID 64048—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物4-[(3-Chloropropyl)sulfanyl]pyridineHCID 15816984—
溶媒DimethylformamideHCID 6228—
生成物3-[3-(4-pyridylthio)propyl]quinazoline-2,4(1H,3H)-dioneHCID 1907909231.1%

反応条件

温度80 °C

反応手順

To a solution of 1.62 g (10 mmol) of benzoylene urea and 1.88 g (10 mmol) of 4-(3-chloropropylthio)pyridine in 50 ml of dimethylformamide, 1.65 ml (11 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added, and the mixture was stirred at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate/ethanol =25:1 to 10:1 to 2:1). First, 0.973 g of 3-[3-(4-pyridylthio)propyl]quinazoline-2,4-(1H,3H)-dione (31.1% yield, pale yellow crystals) was obtained, and then, 0.487 g of the desired product was obtained (10.4% yield, yellow oil).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246948
出典データセットuspto-grants-1993_09
ORD IDord-1dd6d24ee72c4a7caa0ee1e9472a73e8
出典メモuspto-grants-1993_09