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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2096784생성일: 2026년 10월 26일

3-Fluoro-4-(methoxycarbonyl)benzeneboronic acid → 3'-Chloro-4'-[2-(4-ethyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-3-fluoro-biphenyl-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2096784

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluoro-4-(methoxycarbonyl)benzeneboronic acidHCID 2782818—
반응물Trifluoromethanesulfonic acid 3-chloro-4-[2-(4-ethyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-phenyl esterHCID 86645873—
생성물3'-Chloro-4'-[2-(4-ethyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-3-fluoro-biphenyl-4-carboxylic acid methyl esterHCID 67546502—

반응 단계

In analogy to Example 64, step 7, trifluoromethanesulfonic acid 3-chloro-4-[2-(4-ethyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-3,3,3-trifluoro-2-hydroxy-1-methyl-propyl]-phenyl ester (Example 64, step 6) was reacted with 3-fluoro-4-(methoxycarbonyl)phenylboronic acid (70° C., 5.5 h) to give the title compound as a white solid. MS (m/e)=566.3 [M+H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08450313B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-e360ad7f7f054604ae2268181e41a9d1
출처 메모uspto-grants-2013_05