Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 503865생성일: 2026년 10월 26일
1-[4-(4-Chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-(3-iodo-pyrazolo[3,4-b]pyridin-1-yl)-ethanone → 1-{2-[4-(4-Chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-1H-pyrazolo[3,4-b]pyridine-3-carbonitrile
https://huagongshe.com/reaction/503865
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-[4-(4-Chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-(3-iodo-pyrazolo[3,4-b]pyridin-1-yl)-ethanone | HCID 16006031 | — |
| 반응물 | HCID 178418546 | HCID 178418546 | — |
| 용매 | 1-Methyl-2(1H)-pyridinone | HCID 12755 | — |
| 생성물 | 1-{2-[4-(4-Chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-1H-pyrazolo[3,4-b]pyridine-3-carbonitrile | HCID 16005529 | — |
반응 단계
1-[4-(4-Chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-(3-iodo-pyrazolo[3,4-b]pyridin-1-yl)-ethanone (128 Mg) and CuCN (112 Mg) were combined in N-methylpyridone (NMP) (1 mL) and heated at 165° C. for 16 hr, then cooled to room temperature. The reaction mixture was purified on preparative HPLC to afford 1-{2-[4-(4-Chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-1H-pyrazolo[3,4-b]pyridine-3-carbonitrile as a white powder: LCMS (ES) M+H411.5, Rf 2.33 min (Agilent Zorbax SB-C18, 2.1×50 Mm, 5μ, 35° C., 1 mL/min flow rate, a 2.5 min gradient of 20% to 100% B with a 1.1 min wash at 100% B; A=0.1% formic acid/5% acetonitrile/94.9% water, B=0.1% formic acid/5% water/94.9% acetonitrile).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07777035B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-8ff8461440a94c54a90306c17dfd3678 |
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| 출처 메모 | uspto-grants-2010_08 |
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