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HRID 1870613作成日:2026年10月25日

Sodium Carbonate → 1-Ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidine

https://huagongshe.com/reaction/1870613

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物1-Chloro-4-fluoro-2-nitrobenzeneHCID 67659—
反応物2,5-DifluoronitrobenzeneHCID 67767—
反応物Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
溶媒CyclohexanolHCID 7966—
溶媒Ethyl AcetateHCID 8857—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物1-Ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidineHCID 13792162—

反応手順

A solution of ethyl 4-amino-1-piperidine carboxylate (9.0 g, 52 mmol.) and 2-chloro-5-fluoronitrobenzene (10.3g, 58 mmol.) in cyclohexanol (30 mL) containing powdered sodium carbonate (6.1 g, 57 mmol.) was refluxed (>160° C.) for 30 hours or until no further reaction was indicated by tlc(30% EtOAc/hexane). (Alternatively, 2,5-difluoronitrobenzene can be used in place of the 2-chloro-5-fluoronitrobenzene). The deep reddish reaction mixture was cooled and diluted with EtOAc. This solution was washed with dil. aq. HCl (3×), water, and then the organic layer dried (anhydrous Na2SO4) and the solvent evaporated to give a red oil. This oil was flash chromatographed on a column of silica gel and the product eluted with a 10-25% EtOAc/hexane gradient. The appropriate fractions were combined, the solvents evaporated, and the residue triturated with 10% Et2O/hexane to give 1-ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)-piperidine as a bright reddish-orange solid, mp: 115-116° C., which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06096763
出典データセットuspto-grants-2000_08
ORD IDord-1979dfeaca7f4af9a06fa90dc988f1eb
出典メモuspto-grants-2000_08