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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407922생성일: 2026년 10월 24일

Sodium Carbonate → (S)-tert-butyl 3-(2,5-difluoro-4-(methylsulfonyl)phenylamino)-2-oxo-1,4'-bipiperidine-1'-carboxylate

https://huagongshe.com/ko/reaction/407922

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1,2,4-Trifluoro-5-(methylsulfonyl)benzeneHCID 46739396—
반응물(S)-tert-butyl 3-amino-2-oxo-1,4'-bipiperidine-1'-carboxylateHCID 66802275—
용매DimethylformamideHCID 6228—
생성물(S)-tert-butyl 3-(2,5-difluoro-4-(methylsulfonyl)phenylamino)-2-oxo-1,4'-bipiperidine-1'-carboxylateHCID 6747043572.3%

반응 조건

온도130 °C

반응 단계

(S)-tert-butyl 3-amino-2-oxo-1,4′-bipiperidine-1′-carboxylate (4.0 g, 13 mmol), 1,2,4-trifluoro-5-(methylsulfonyl)benzene (Preparation C, 4.2 g, 20 mmol) and Na2CO3 (2.9 g, 27 mmol) were dissolved in DMF (30 mL) and heated at 130° C. overnight. The reaction was concentrated and purified over silica gel (25-75% EtOAc in hexanes) to afford (S)-tert-butyl 3-(2,5-difluoro-4-(methylsulfonyl)phenylamino)-2-oxo-1,4′-bipiperidine-1′-carboxylate (4.6 g, 9.4 mmol, 70% yield) as yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754226B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-95ac0d79b0024d8f8fdbe390394d4565
출처 메모uspto-grants-2014_06