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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447279생성일: 2026년 10월 25일

Piperidine → (E)-3-((3-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-6-yl)methylene)indolin-2-one

https://huagongshe.com/reaction/447279

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물OxindoleHCID 321710—
반응물3-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole-6-carbaldehydeHCID 58189696—
용매EthanolHCID 702—
생성물(E)-3-((3-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-6-yl)methylene)indolin-2-oneHCID 58486274—

반응 조건

온도70 °C

반응 단계

Oxindole (665 mg, 5 mmol) and 3-iodo-1-((2-(trimethylsilyl)ethoxy) methyl)-1H-indazole-6-carbaldehyde (2 g, 5 mmol) were dissolved into ethanol (25 mL). Piperidine (0.1 mL) was added and the solution was heated to 70° C. for 2 h, cooled to rt and stirred overnight. The solvent was removed in vacuo to give an orange solid which was triturated with ethanol to give the title compound in quantitative yield. 1H NMR (400 MHz, CDCl3) δ 7.95 (s, 1H), 7.86 (s, 1H), 7.62-7.55 (m, 3H), 7.24 (d, 1H, J=7.8 Hz), 6.91 (d, 1H, J=7.8 Hz), 6.86 (t, 1H, J=7.6 Hz), 5.75 (s, 2H), 3.62-3.58 (m, 2H), 0.93-0.89 (m, 2H), −0.04 (s, 9H); MS ESI 518.0 [M+H]+, calcd for [C22H24IN3O2Sii+H]+ 518.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481533B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-50267baa086f4c828759d099779ced83
출처 메모uspto-grants-2013_07