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HRID 1504231作成日:2026年10月26日

Sodium hydride → 7-[3-(3-bromo-2-oxo-2H-quinolin-1-yl)propoxy]-1-ethyl-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione

https://huagongshe.com/reaction/1504231

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Lithium BromideHCID 82050—
反応物3-Bromoquinolin-2-olHCID 268338—
反応物1-Ethyl-7-(3-iodopropoxy)-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dioneHCID 68672792—
溶媒DimethylformamideHCID 6228—
生成物7-[3-(3-bromo-2-oxo-2H-quinolin-1-yl)propoxy]-1-ethyl-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dioneHCID 6696161251.1%

反応条件

温度0 °C

反応手順

Under ice cooling, sodium hydride (60% in oil, 0.2 g) was added to a DMF solution(10 ml) of 3-bromo-1H-quinoline-2-one(1.0 g). The mixture was stirred at the same temperature for 15 minutes. Lithium bromide(0.76 g) was added to the mixture, and the liquid was stirred at the same temperature for another 15 minutes, and then at room temperature for an hour. The reaction mixture was cooled to 0° C., and 1-ethyl-7-(3-iodopropoxy)-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione(2.1 g) was added thereto. The mixture was stirred at room temperature for 2 hours, and at 50° C. for 8 hours. The reaction mixture was poured to ice water, and the generated insoluble matter was separated. The insoluble matter was dissolved in a mixed solvent of ethyl acetate and dichloromethane. The liquid was dried with sodium sulfate and condensed under reduced pressure. Ethyl acetate was added to the residue. The generated insoluble matter was separated and dried to give the title compound(1.2 g) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09212187B2
出典データセットuspto-grants-2015_12
ORD IDord-02600dbd312a4ebb95b293d966f0c8ff
出典メモuspto-grants-2015_12