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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131663생성일: 2026년 10월 25일

3-Fluoro-4-methoxyaniline → N-(3-Fluoro-4-methoxyphenyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carboxamide

https://huagongshe.com/reaction/131663

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluoro-4-methoxyanilineHCID 581110—
반응물2'-Methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carbonyl chlorideHCID 21078801—
생성물N-(3-Fluoro-4-methoxyphenyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carboxamideHCID 10202066—

반응 단계

N-(3-Fluoro-4-methoxyphenyl)-2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxamide was prepared from 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carbonyl chloride and 3-fluoro-4-methoxyaniline using method K. NMR; δH [2H6]—DMSO 10.35,(1H, b), 8.04,(2H, d), 7.90,(1H, dd), 7.78-7.75,(2H, m)7.59-7.51,(4H, m), 7.17,(1H, t), 3.82,(3H, s), 2.57,(3H, s), 2.33,(3H, s). LCMS; retention time 3.50 min, MH+ 418.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384963B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-8a079f4977294d21b9430b38071b1e2f
출처 메모uspto-grants-2008_06