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HRID 1467963생성일: 2026년 10월 27일

Acetic Acid → Tert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1467963

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물6-Bromopyridin-3-amineHCID 642811—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,1-DichloroethaneHCID 6365—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylateHCID 8660214062%

반응 단계

To a mixture of tert-butyl 4-oxopiperidine-1-carboxylate (1.15 g, 5.78 mmol) and 6-bromopyridin-3-amine (0.5 g, 2.89 mmol) in dichloroethane (20 mL), acetic acid (8 mL, 2.89 mmol) was added and the contents were stirred at room temperature for 3 h. Sodium triacetoxy borohydride (1.225 g, 5.78 mmol) was added and the contents were stirred at room temperature for 12 h. The reaction was diluted with ethyl acetate and washed with brine; the organic layer was separated and concentrated in vacuo. The resulting residue was purified by flash column chromatography to give tert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylate (0.638 g, 62%); MS: 357.1 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09000175B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-095a9df2de08454da67543e86e1307a9
출처 메모uspto-grants-2015_04