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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1262246생성일: 2026년 10월 27일

3-(3-Aminophenyl)-1,4-dimethylpiperazin-2-one → 3-{3-[7-(6-Methoxy-pyridin-3-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-phenyl}-1,4-dimethyl-piperazin-2-one

https://huagongshe.com/reaction/1262246

반응식

참여 물질

역할이름HCID투입량
반응물3-(3-Aminophenyl)-1,4-dimethylpiperazin-2-oneHCID 57416081—
반응물HCID 178488500HCID 178488500—
생성물3-{3-[7-(6-Methoxy-pyridin-3-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-phenyl}-1,4-dimethyl-piperazin-2-oneHCID 66712249—

반응 단계

3-{3-[7-(6-Methoxy-pyridin-3-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-phenyl}-1,4-dimethyl-piperazin-2-one was prepared from 7-(6-methoxy-pyridin-3-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-ol and 3-(3-amino-phenyl)-1,4-dimethyl-piperazin-2-one in an analogous manner to Example 1052a. Product isolated as a brown foam (56 mg, 42%). LCMS (m/e) 444 (M+H); 1H-NMR (CDCl3, 400 MHz) δ 8.80-8.74 (m, 1H), 8.69 (s, 1H), 8.43 (dd, 1H, J=2.2 and 8.7 Hz), 7.66 (d, 1H, J=8.1 Hz), 7.51 (s, 1H), 7.35-7.27 (m, 1H), 7.06 (d, 1H, J=7.6 Hz), 6.96-6.89 (m, 2H), 6.87 (d, 1H, J=8.7 Hz), 6.82 (d, 1H, J=4.78 Hz), 4.01 (s, 3H), 3.75-3.63 (m, 2H), 3.25-3.16 (m, 1H), 3.07-2.96 (m, 1H), 2.98 (s, 3H), 2.74-2.63 (m, 1H), 2.21 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08471005B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-5b773897ce834f81a22ae3de4e96f8f3
출처 메모uspto-grants-2013_06