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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1037421생성일: 2026년 10월 25일

2-Cyano-3-fluorophenylboronic acid pinacol ester → tert-butyl (1-(4-(8-(2-cyano-3-fluorophenyl)-4-oxo-2-phenyl-4H-pyrano[2,3-c]pyridin-3-yl)phenyl)cyclobutyl)carbamate

https://huagongshe.com/reaction/1037421

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyano-3-fluorophenylboronic acid pinacol esterHCID 22273603—
반응물3-(4-(1-aminocyclobutyl)phenyl)-8-(1-isobutyl-1H-pyrazol-4-yl)-2-phenyl-4H-pyrano[2,3-c]pyridin-4-oneHCID 67067767—
반응물tert-Butyl 1-(4-(8-chloro-4-oxo-2-phenyl-4H-pyrano[2,3-c]pyridin-3-yl)phenyl)cyclobutylcarbamateHCID 86671031—
생성물tert-butyl (1-(4-(8-(2-cyano-3-fluorophenyl)-4-oxo-2-phenyl-4H-pyrano[2,3-c]pyridin-3-yl)phenyl)cyclobutyl)carbamateHCID 8667106144%

반응 단계

Following the procedure used to prepare 3-(4-(1-aminocyclobutyl)phenyl)-8-(1-isobutyl-1H-pyrazol-4-yl)-2-phenyl-4H-pyrano[2,3-c]pyridin-4-one, tert-butyl 1-(4-(8-chloro-4-oxo-2-phenyl-4H-pyrano[2,3-c]pyridin-3-yl)phenyl)cyclobutylcarbamate was reacted with 2-fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile to give the title compound (40 mg, 44%). LCMS (Method I): RT=7.90 min, [M+H]+=532 (-tBu).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08546376B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-626b5a21c2964c5da31dca1c7bf6569e
출처 메모uspto-grants-2013_10