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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62097생성일: 2026년 10월 23일

3,4-Diaminopyridine → 3-(3H-imidazo[4,5-c]pyridin-2-yl)-5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/ko/reaction/62097

반응식

참여 물질

역할이름HCID투입량
반응물3,4-DiaminopyridineHCID 5918—
반응물SulfurHCID 5362487—
반응물5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-3-carbaldehydeHCID 58378078—
용매DimethylformamideHCID 6228—
생성물3-(3H-imidazo[4,5-c]pyridin-2-yl)-5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridineHCID 136193591—

반응 단계

A solution of 5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde (LVII) (0.120 g, 0.37 mmol), 3,4-diaminopyridine (LVIII) (42 mg, 0.39 mmol) and sulfur (13 mg, 0.39 mmol) in dry DMF (5 mL) was heated at 140° C. under nitrogen for 12 h. The solution was cooled to room temperature and the solvent was evaporated under reduced pressure. The residue was dissolved in DCM and washed with water (1×20 mL). The organic layer was dried over MgSO4, filtered and concentrated to yield 3-(3H-imidazo[4,5-c]pyridin-2-yl)-5-(4-methylpyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine (LIX). The crude product was used directly for step 3 without further purification. ESIMS found for C23H21N7O m/z 412.7 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446035B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-55b641bad9374ff2ba66f8c1660fc04f
출처 메모uspto-grants-2016_09