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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74901생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/74901

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ammonium BicarbonateHCID 14013—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물1-((Tert-butoxy)carbonyl)-4,4-difluoropiperidine-2-carboxylic acidHCID 10106900—
용매1,4-DioxaneHCID 31275—
생성물Tert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylateHCID 67286514—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829007B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e7fe087c2d5d46bab2cfd714b40831b4
출처 메모uspto-grants-2014_09