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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74488생성일: 2026년 10월 24일

Trifluoroacetic acid → Benzyl 4-(2-chloro-pyridin-3-yl-amino)-piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/74488

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium HydroxideHCID 14798—
반응물2-Chloro-3-pyridylamineHCID 80528—
반응물Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Isopropyl AcetateHCID 7915—
생성물Benzyl 4-(2-chloro-pyridin-3-yl-amino)-piperidine-1-carboxylateHCID 46853853—

반응 단계

560 mL (7.25 mol) TFA were added dropwise at approx. 15° C. to 930 g (3.99 mol) N-benzyloxy carbonyl-4-piperidone and 466 g (3.63 mol) 2-chloro-3-aminopyridine in 9.5 L isopropyl acetate. 922 g (4.35 mol) sodium triacetoxyborohydride were added batchwise. The mixture was stirred until the reaction was complete. At RT the reaction mixture was combined with 860 mL sodium hydroxide solution (2 mol/L). The organic phase was separated off, washed with 5 L water and evaporated down.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829006B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a06270afeed240be97e9dcae3d8058fa
출처 메모uspto-grants-2014_09