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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 457555생성일: 2026년 10월 25일

Tetrahydrofuran → 8-(4-Iodo-2-methoxy-pyridin-3-yl)-6-methyl-2-morpholin-4-yl-9H-purine

https://huagongshe.com/reaction/457555

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Iodo benzene diacetateHCID 12217721—
반응물N5-(4-Iodo-2-methoxy-pyridin-3-ylmethylene)-6-methyl-2-morpholin-4-yl-pyrimidine-4,5-diamineHCID 58819980—
용매MethanolHCID 887—
생성물8-(4-Iodo-2-methoxy-pyridin-3-yl)-6-methyl-2-morpholin-4-yl-9H-purineHCID 17849418636%

반응 단계

To a solution of N5-(4-Iodo-2-methoxy-pyridin-3ylmethylene)-6-methyl-2-morpholin-4-yl-pyrimidine-4,5-diamine (140 mg, 0.31 mmol) in a mixture of MeOH:THF (20 mL: 10 mL) was added iodobenzene diacetate (198 mg, 0.62 mmol). After stirring at ambient temperature for 4 hours, the solvents were evaporated in vacuo and the crude was purified by preparative HPLC (see method below) to give the title compound as an amber solid (50 mg, 36%): IR (KBr, cm−1) 3420, 2853, 1618; 1H NMR (400 MHz, CDCl3) δ 9.63 (s, 1H), 7.83 and 7.54 (d, J=5.3, 1H), 3.91 (s, 3H), 3.81–3.77 (m, 8H), 2.72 (s, 3H); LCMS (+ESI, M+H+) m/z 453; HPLC: 97% (220 nm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189716B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-3f6a966281734c0e8afd9d502cafa527
출처 메모uspto-grants-2007_03