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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386567생성일: 2026년 10월 25일

Isobutane → tert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/386567

반응식

참여 물질

역할이름HCID투입량
반응물IsobutaneHCID 6360—
반응물Methyl 4-(1-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 44620996—
반응물1-(4-(Methylsulfonyl)phenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 86658658—
생성물tert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylateHCID 6744541691%

반응 단계

tert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylate was prepared in 91% yield according to procedures described in Example 31 (Step A) substituting methyl 441-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-(methylsulfonyl)phenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylate for methyl 4-(1-(tert-butoxycarbonyl)piperidin-4-yloxy)-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazine-3-carboxylate (example 29). MS (ESI) 402 (M+H-tBu).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372837B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-b3d7758759f2471b81a8c11237c59839
출처 메모uspto-grants-2013_02