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HRID 2064124作成日:2026年10月26日

Water → 1,1-Dimethylethyl 4-[(5-chloro-4-methyl-2-nitrophenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/2064124

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DiisopropylethylamineHCID 81531—
反応物1,5-Dichloro-2-methyl-4-nitrobenzeneHCID 251679—
反応物4-Amino-1-Boc-piperidineHCID 1268291—
溶媒DimethylformamideHCID 6228—
生成物1,1-Dimethylethyl 4-[(5-chloro-4-methyl-2-nitrophenyl)amino]-1-piperidinecarboxylateHCID 59850138—

反応条件

温度100 °C

反応手順

1,5-Dichloro-2-methyl-4-nitrobenzene (2.42 mmol, 500 mg) was dissolved in dry dimethylformamide (5 ml) and diisopropylethylamine (1 eq., 2.42 mmol, 0.413 ml), 1,1-dimethylethyl 4-amino-1-piperidinecarboxylate (1 eq., 2.42 mmol, 484 mg) were added at room temperature and the mixture was stirred at 100° C. overnight. The crude mixture was then cooled to room temperature and water was added; the aqueous solution was extracted with ethyl acetate (3×); organics were alternatively washed with brine and water. The organics were combined, dried over Na2SO4, filtered and the solvent was evaporated to afford the crude compound that was purified by chromatography (ethyl acetate/hexane) to yield the title compound, 98 mg, 11%, bright orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08288412B2
出典データセットuspto-grants-2012_10
ORD IDord-299f2183c10d4f508b68f534b983dc8b
出典メモuspto-grants-2012_10