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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131672생성일: 2026년 10월 26일

4-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic Acid → 2'-Methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(3-[(3-phenylureido)methyl]phenyl}-1,1'-biphenyl-4-carboxamide

https://huagongshe.com/reaction/131672

반응식

참여 물질

역할이름HCID투입량
반응물4-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic AcidHCID 11220119—
반응물N-(3-aminobenzyl)-N'-phenylureaHCID 59190887—
생성물2'-Methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(3-[(3-phenylureido)methyl]phenyl}-1,1'-biphenyl-4-carboxamideHCID 10229641—

반응 단계

2′-Methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-N-{3-[(3-phenylureido)methyl]phenyl}-1,1′-biphenyl-4-carboxamide was prepared from 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxylic acid and N-(3-aminobenzyl)-N′-phenylurea using method J. NMR; δH [2H6]—DMSO 10.36,(1H, b), 8.57,(1H, s), 8.06,(2H, d), 7.90,(1H, dd), 7.78,(2H, m), 7.69,(1H, dd), 7.57,(3H, m), 7.39,(3H, m), 7.21,(2H, m), 7.05,(1H, d), 6.62,(1H, t), 4.31,(2H, d), 2.57,(3H, s), 2.33,(3H, s). LCMS; retention time 3.55 min, MH+ 518.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384963B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-2b9e7fc1a92849c79815f7a82b4e5c7b
출처 메모uspto-grants-2008_06