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HRID 333962作成日:2026年10月26日

N,N-Dimethylaniline → 1-(3-Methoxy-2-methyl-4-pyridyl)piperazine

https://huagongshe.com/reaction/333962

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物PiperazineHCID 4837—
反応物3-(3-Methoxypropoxy)-1-propanolHCID 66984—
反応物4-Chloro-3-methoxy-2-methylpyridineHCID 10583046—
生成物1-(3-Methoxy-2-methyl-4-pyridyl)piperazineHCID 6683561394.1%

反応条件

温度140 °C

反応手順

4-Chloro-3-methoxy-2-methyl-pyridine (0.47 g, 3 mmol) was mixed with dipropyleneglycolmonomethylether (3 ml), piperazine (1.1 g, 7.2 mmol) and N,N-dimethylaniline (0.36 g, 3 mmol) and stirred at 140° C. for 72 hours. The solvent was removed under reduced pressure and the residue was purified by column chromatography (prepacked silica column, gradient ethyl acetate/methanol with the addition of 1% ammonia). The raw product was dissolved in 1M NaOH and extracted with a mixture of diethylether, dichloromethane and ethylacetate (1:1:1) several times. The combined organic phases were washed with water, dried over sodium sulfate, and the solvent was removed under reduced pressure to yield 585 mg of a yellow solid (2.8 g, 94%). MS (APCI): m/z=208.0 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883791B2
出典データセットuspto-grants-2014_11
ORD IDord-fd595ac2c5bc423eb5643a5e9bd250f5
出典メモuspto-grants-2014_11