Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521767생성일: 2026년 10월 25일
methyl 5-(4-((3-nitrophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate → methyl 5-(4-((3-aminophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate
https://huagongshe.com/reaction/521767
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | methyl 5-(4-((3-nitrophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate | HCID 67042295 | — |
| 용매 | Ethanol ethylacetate | HCID 21584252 | — |
| 생성물 | methyl 5-(4-((3-aminophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate | HCID 67042564 | 96% |
반응 단계
Methyl 5-(4-((3-nitrophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate (1.32 g, 3.9 mmol) was taken up in EtOAc/EtOH (1:1; 90 mL) and purged with N2. Pd/C (10%, 0.145 g) was added and the mixture was stirred under an atmosphere of H2 at rt for 18 h. The mixture was filtered over celite, washing with EtOAc/EtOH. The filtrate was concentrated, taken back up in EtOAc and filtered over celite again to remove any residual catalyst. The filtrate was concentrated again and taken back up in EtOAc. The solution was filtered and the filtrate was concentrated to afford a tan solid. The solid was washed with CH2Cl2/hexanes (1:2) and dried under high vacuum to afford methyl 5-(4-((3-aminophenyl)amino)pyridin-2-yl)-1H-pyrrole-3-carboxylate (1.15 g, 96% yield) as a tan solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09328103B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-c76ba6c860a4497788c898491266d028 |
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| 출처 메모 | uspto-grants-2016_05 |
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