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HRID 530008作成日:2026年10月27日

2-Iodobenzoic acid → Methyl 2-((4'-amino-3,3'-dimethoxy-[1,1'-biphenyl]-4-yl)amino)benzoate

https://huagongshe.com/reaction/530008

反応式

関与物質

役割名称HCID仕込み量
反応物2-Iodobenzoic acidHCID 6941—
反応物DianisidineHCID 8411—
反応物Cesium carbonateHCID 10796—
反応物2-((4'-((2-carboxyphenyl)amino)-3,3'-dimethoxy-[1,1'-biphenyl]-4-Yl)amino)-5-methylbenzoic acidHCID 57519836—
触媒Pd2(dba)3 DPPPHCID 86670201—
溶媒TolueneHCID 1140—
生成物Methyl 2-((4'-amino-3,3'-dimethoxy-[1,1'-biphenyl]-4-yl)amino)benzoateHCID 57519834—

反応手順

Compound Ic-7 can be synthesixed by reacting commercially available 3,3′-dimethoxy-[1,1′-biphenyl]4,4′-diamine (1 equivalent) with 1.2 equivalents of the commercially available methyl ester of iodobenzoic acid in the presence of Pd2(dba)3/DPPP (0.1-0.5 equiv) and 1.2 equivalents Cs2CO3 in toluene at 110° C. for 20 h with vigorous stirring. The intermediate compound methyl 2-((4′-amino-3,3′-dimethoxy-[1,1′-biphenyl]-4-yl)amino)benzoate is isolated by flash chromatography on a C18 column. The product is then reacted by addition of 1.2 equivalent of methyl 2-iodo-5-methylbenzoate in the presence of catalytic (0.1-0.5 equiv) Pd2(dba)3/DPPP and 1.2 equivalents anhydrous, finely powdered Cs2CO3 in toluene at 110° C. for 20 h to yield methyl 2-((3,3′-dimethoxy-4′-((2-(methoxycarbonyl)phenyl)amino)-[1,1′-biphenyl]-4-yl)amino)-5-methylbenzoate. The methyl esters can then be hydrolyzed under basic conditions followed by acidification to yield compound Ic-7, 2-((4′-((2-carboxyphenyl)amino)-3,3′-dimethoxy-[1, 1′-biphenyl]-4-yl)amino)-5-methylbenzoic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09351971B2
出典データセットuspto-grants-2016_05
ORD IDord-5c23d420c62045e68db9a3d4808304ec
出典メモuspto-grants-2016_05