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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1518493생성일: 2026년 10월 26일

1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine → Tert-butyl 4-(5-chloro-1-(4-cyano-3-fluorophenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1518493

반응식

참여 물질

역할이름HCID투입량
반응물1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
반응물4,6-DihydroxynicotinonitrileHCID 54706325—
반응물4-(5-chloro-4-hydroxy-2-oxopyridin-1(2H)-yl)-2-fluorobenzonitrileHCID 67366532—
반응물1-(5-Propylpyrimidin-2-yl)piperidin-4-ylmethanesulfonateHCID 86658030—
생성물Tert-butyl 4-(5-chloro-1-(4-cyano-3-fluorophenyl)-2-oxo-1,2-dihydropyridin-4-yloxy)piperidine-1-carboxylateHCID 57468467—

반응 단계

The intermediate was prepared according to the procedures described in Example 221 substituting 4-(5-chloro-4-hydroxy-2-oxopyridin-1(2H)-yl)-2-fluorobenzonitrile for 4-hydroxy-6-oxo-1,6-dihydropyridine-3-carbonitrile and tert-butyl 4-(methylsulfonyloxy)piperidine-1-carboxylate for 1-(5-propylpyrimidin-2-yl)piperidin-4-ylmethanesulfonate in Step B. MS (ESI) 392 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232404B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-f67ae656b49c4deaae98e59761787134
출처 메모uspto-grants-2012_07