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HRID 428541作成日:2026年10月24日

Water → 6-Bromo-8-piperazin-1-yl-quinoline

https://huagongshe.com/ja/reaction/428541

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Chloroethyl chloroformateHCID 12305—
反応物Vinyl chloroformateHCID 78808—
反応物8-(4-Benzyl-piperazin-1-yl)-6-bromo-quinolineHCID 18414079—
溶媒1,1-DichloroethaneHCID 6365—
生成物6-Bromo-8-piperazin-1-yl-quinolineHCID 1841406384%

反応条件

温度80 °C

反応手順

To a solution of 8-(4-benzyl-piperazin-1-yl)-6-bromo-quinoline (1.6 g, 4.2 mmol) in dichloroethane (50 mL) under a N2 atmosphere was added chloroethylchloroformate (1.26 mL, 12.6 mmol) and the reaction mixture was heated at 80° C. for 4 hours, and at ambient temperaure overnight. No reaction was observed by TLC, therefore vinyl chloroformate (0.35 mL, 6.3 mmol) was added and the reaction was heated at 80° C. for another 4 hours. The cooled reaction was poured into H2O and extracted into CH2Cl2 (2×100 mL) and EtOAc (100 mL). The organic fractions were combined, dried over Na2SO4, and left in EtOAc overnight. The organic layer was concentrated and purified by column chromatography 10%MeOH/CH2C2+NH4OH) affording 1.03 g (84%) of a brown foam. MS(+)APCI m/z 292 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313126B1
出典データセットuspto-grants-2001_11
ORD IDord-f89bd88f9d2248a5ae5909fa844d6f8d
出典メモuspto-grants-2001_11