Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 530008생성일: 2026년 10월 25일
2-Iodobenzoic acid → Methyl 2-((4'-amino-3,3'-dimethoxy-[1,1'-biphenyl]-4-yl)amino)benzoate
https://huagongshe.com/reaction/530008
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Iodobenzoic acid | HCID 6941 | — |
| 반응물 | Dianisidine | HCID 8411 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 2-((4'-((2-carboxyphenyl)amino)-3,3'-dimethoxy-[1,1'-biphenyl]-4-Yl)amino)-5-methylbenzoic acid | HCID 57519836 | — |
| 촉매 | Pd2(dba)3 DPPP | HCID 86670201 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Methyl 2-((4'-amino-3,3'-dimethoxy-[1,1'-biphenyl]-4-yl)amino)benzoate | HCID 57519834 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09351971B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-5c23d420c62045e68db9a3d4808304ec |
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| 출처 메모 | uspto-grants-2016_05 |
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