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HRID 131683作成日:2026年10月27日

4-Hydroxybenzylamine → N-(4-Hydroxybenzyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carboxamide

https://huagongshe.com/reaction/131683

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzylamineHCID 97472—
反応物4-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic AcidHCID 11220119—
生成物N-(4-Hydroxybenzyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1'-biphenyl-4-carboxamideHCID 10200939—

反応手順

N-(4-Hydroxybenzyl)-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-carboxylic acid and 4-hydroxybenzylamine using method H. NMR; δH [2H6]—DMSO 9.27,(1H, s), 9.02,(1H, t), 7.98,(2H, d), 7.89,(1H, dd), 7.76,(1H, d), 7.54,,(1H, d), 7.51,(2H, d), 7.13,(2H, d), 6.71,(2H, d), 4.39,(2H, d), 2.56,(3H, s), 2.31,(3H, s), LCMS; retention time 3.03 min, MH+ 400.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384963B2
出典データセットuspto-grants-2008_06
ORD IDord-917d1a4daf16441e8018ffb6fc38fd78
出典メモuspto-grants-2008_06