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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276763생성일: 2026년 10월 25일

Stannane → 3-(Furan-2-yl)-7-(5-methylisoxazol-3-yl)-2-(1-methyl-1H-[1,2,4]triazol-5-ylmethoxy)pyrazolo[1,5-d][1,2,4]triazine

https://huagongshe.com/reaction/276763

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참여 물질

역할이름HCID투입량
반응물StannaneHCID 123161—
반응물2-(Tributylstannyl)furanHCID 4393688—
반응물3-Bromo-7-(5-methylisoxazol-3-yl)-2-(1-methyl-1H-[1,2, 4]triazol-5-ylmethoxy)pyrazolo[1,5-d][1,2,4]triazineHCID 22629146—
촉매PalladiumHCID 23938—
용매1,4-DioxaneHCID 31275—
생성물3-(Furan-2-yl)-7-(5-methylisoxazol-3-yl)-2-(1-methyl-1H-[1,2,4]triazol-5-ylmethoxy)pyrazolo[1,5-d][1,2,4]triazineHCID 22629140196.9%

반응 단계

A stirred mixture of 3-bromo-7-(5-methylisoxazol-3-yl)-2-(1-methyl-1H-[1,2,4]triazol-5-ylmethoxy)pyrazolo[1,5-d][1,2,4]triazine (Example 7) (80 mg, 0.20 mmol) in dioxan (10 mL) containing 2-tri-n-butylstannylfuran (146 mg, 0.41 mmol) was degassed with nitrogen for 20 min. Tetrakis-triphenylphosphine palladium(0) (50 mg) and copper(I)iodide (5 mg) were added and the mixture heated at reflux for 8 h. Further stannane (146 mg, 0.41 mmol) and palladium catalyst (50 mg) were added and the mixture heated at reflux for 16 h. The solvent was evaporated and the residue purified on silica eluting with 5% MeOH/DCM to give a yellow solid (149 mg). The yellow solid was re-chromatographed on silica eluting with 5% MeOH/DCM to give a yellow solid (29 mg) which was triturated with diethylether to give the title compound (15 mg, 19%) as a yellow solid. mp 226-228° C. 1H NMR (360 MHz, CDCl3) δ1.58 (9H, s), 2.61 (3H, s), 4.10 (3H, s), 5.78 (2H, s), 6.52-6.56 (1H, m), 6.75-6.79 (1H, m), 6.96 (1H, s), 7.57 (1H, s), 7.91 (1H, s), 9.71 (1H, s). Found: C, 52.68; h, 3.47; N, 28.64; C17H14N8O3.0.05(CH2Cl2).0.25(H2O) requires: C, 52.90; H, 28.95%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355638B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-a07aef879027416f8f6d1cfa8487eda3
출처 메모uspto-grants-2002_03