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HRID 333960作成日:2026年10月26日

tert-Butyl piperazine-1-carboxylate → (8-Methyl-4-quinolyl)piperazine

https://huagongshe.com/reaction/333960

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物4-Chloro-8-methylquinolineHCID 12326335—
溶媒3-(3-Methoxypropoxy)-1-propanolHCID 66984—
生成物(8-Methyl-4-quinolyl)piperazineHCID 4384050880%

反応条件

温度140 °C

反応手順

8-Methyl-4-chloroquinoline (355 mg, 2 mmol) was suspended in dipropyleneglycolmonomethylether (4 ml), a solution of tert-butyl piperazine-1-carboxylate (440 mg, 2.4 mmol) in dipropyleneglycolmonomethylether (4 ml) was added and the mixture was stirred at 140° C. overnight and the solvent was evaporated under reduced pressure. The residue was dissolved in a mixture of dichloromethane and trifluoroacetic acid (1:1, 4 ml) and stirred at room temperature for 90 minutes. The mixture was evaporated to dryness under reduced pressure and the residue was dissolved in dichloromethane. The solution was washed with 5% sodium bicarbonate solution and water, dried over sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by column chromatography (prepacked silica column, gradient ethyl acetate/methanol with the addition of 1% ammonia) to yield 364 mg of a solid (1.6 mmol, 80%). MS (APCI): m/z=227.9 [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-b009f21a1158469280fafeb63b31bca4
出典メモuspto-grants-2014_11