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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452040생성일: 2026년 10월 25일

Potassium Carbonate → 5-(3-amino-1,2,4-triazin-6-yl)-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/452040

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물6-Bromo-1,2,4-triazin-3-amineHCID 15332564—
반응물N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamideHCID 44119560—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물5-(3-amino-1,2,4-triazin-6-yl)-N-methylpyridine-2-carboxamideHCID 5751653345.7%

반응 조건

온도120 °C

반응 단계

A mixture of N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxamide (200 mg, 0.80 mmol) (VWR, Cat. #200068-640), 6-bromo-1,2,4-triazin-3-amine (130 mg, 0.76 mmol, Example 2, Step 1), tetrakis(triphenylphosphine)palladium(0) (40 mg, 0.04 mmol) and potassium carbonate (0.32 g, 2.3 mmol) in toluene (1.3 mL), ethanol (0.66 mL) and water (0.66 mL) was heated at 120° C. for 1.5 h. The mixture was filtered and washed with methanol. The filtrate was purified by RP-HPLC (pH=10) to afford the desired product (80 mg, 45.54%). LCMS (M+H)+: m/z=231.4; LCMS (M+H+H2O)+: m/z=249.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08487096B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e5414436b6254139a962e9e0923cb320
출처 메모uspto-grants-2013_07