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HRID 883520作成日:2026年10月27日

Hydrochloric Acid → 3-Iodo-8-(4-methyl-piperazin-1-yl)-quinoline

https://huagongshe.com/reaction/883520

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TolueneHCID 1140—
反応物Potassium IodideHCID 4875—
反応物3-Bromo-8-(4-methyl-piperazin-1-yl)-quinolineHCID 67313624—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒HexamethylphosphoramideHCID 12679—
生成物3-Iodo-8-(4-methyl-piperazin-1-yl)-quinolineHCID 67313746—

反応条件

温度150 °C

反応手順

A mixture of 3-bromo-8-(4-methyl-piperazin-1-yl)-quinoline (D1) (1.75 g, 5.7 mmol), copper (I) iodide (5.4 g, 28.5 mmol) and potassium iodide (9.6 g, 57.8 mmol) in hexamethylphosphoramide (20 ml) was heated in an oil bath at 150° C. for 21 h under argon. To the cooled reaction mixture was added toluene (120 ml) and 1M hydrochloric acid (120 ml) and the whole was shaken vigorously for 5 minutes. The insoluble brown solid was then collected by filtration, washed with methanol (3×40 ml) and resuspended in a mixture of dichloromethane (150 ml) and 2M sodium hydroxide (150 ml). After shaking the mixture vigorously, the insoluble material was filtered, washed with dichloromethane (2×50 ml) and discarded. The filtrate and washings were transferred to a separating funnel and the layers were separated. The aqueous phase was extracted with dichloromethane (2×100 ml) and the combined organic extracts were dried (MgSO4) and concentrated to a brown oil (1.5 g) which was identified by NMR spectroscopy as a mixture of the title compound (D2) and 3-bromo-8-(4-methyl-piperazin-1-yl)-quinoline (D1) in a ratio of 4:1. This mixture was used directly in the next stage (see Example 1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236947B2
出典データセットuspto-grants-2012_08
ORD IDord-bf9dace181c54d38bdb8d57d2c952fcf
出典メモuspto-grants-2012_08