戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1183070作成日:2026年10月25日

Triethylamine → 3,3-Diethyl-7-methoxy-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione

https://huagongshe.com/reaction/1183070

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Methoxy-o-phenylenediamineHCID 153404—
反応物Diethylmalonyl dichlorideHCID 4149059—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3,3-Diethyl-7-methoxy-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dioneHCID 6867311734.5%

反応手順

Diethylmalonyl dichloride (0.95 ml, 5.5 mmol) was added to a dichloromethane solution (20 ml) of 4-methoxy-o-phenylenediamine (691 mg, 5 mmol) and triethylamine (1.7 ml, 12.5 mmol) at 0° C., and stirred at room temperature overnight. Water was added to the reaction mixture, and extraction with dichloromethane was performed. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=9:1→1:1). The purified product was concentrated to dryness under reduced pressure to thereby obtain 452.3 mg (yield: 34%) of 3,3-diethyl-7-methoxy-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08664217B2
出典データセットuspto-grants-2014_03
ORD IDord-b38b5b09b5a34e408958c59d1f2b73b4
出典メモuspto-grants-2014_03