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HRID 74901作成日:2026年10月25日

Pyridine → Tert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/74901

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ammonium BicarbonateHCID 14013—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物1-((Tert-butoxy)carbonyl)-4,4-difluoropiperidine-2-carboxylic acidHCID 10106900—
溶媒1,4-DioxaneHCID 31275—
生成物Tert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylateHCID 67286514—

反応手順

To a solution of 1-tert-butoxycarbonyl-4,4-difluoro-piperidine-2-carboxylic acid, 13f, (1.67 g, 6.30 mmol) in 1,4-dioxane (12 mL) was added pyridine (0.35 mL, 4.33 mmol), followed by di-tert-butyl dicarbonate (1.78 g, 8.17 mmol) and ammonium bicarbonate (0.63 g, 7.86 mmol). The reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the residue was taken up in EtOAc. The organic phase was washed with water, aqueous saturated KHSO4 solution, brine, dried over Na2SO4, filtered and evaporated to dryness. The crude residue was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829007B2
出典データセットuspto-grants-2014_09
ORD IDord-e7fe087c2d5d46bab2cfd714b40831b4
出典メモuspto-grants-2014_09