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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73703생성일: 2026년 10월 27일

6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine → 6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amine

https://huagongshe.com/reaction/73703

반응식

참여 물질

역할이름HCID투입량
반응물6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 57955201—
반응물HCID 178477796HCID 178477796—
용매1,4-DioxaneHCID 31275—
생성물6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 5528862179.8%

반응 조건

온도90 °C

반응 단계

To a degassed solution of 6-bromopyrrolo[2,1-f][1,2,4]triazin-4-amine (Intermediate AAE) (316 mg, 1.48 mmol) and Bis(diphenylphosphino)ferrocenepalladium dichloride (30 mg, 0.037 mmol) in 1,4-dioxane (10 mL), was added dimethyl zinc (2.97 mL, 5.93 mmol, 2.0 M in toluene). The mixture was allowed to stir at 90° C. for 17 hr and then cooled to 0° C. The reaction was quenched with MeOH (1.0 mL) and partitioned between ethyl acetate (200 mL) and potassium phosphate dibasic pH 10 buffer (100 mL). The layers were separated and the organic phase was washed with brine, dried (Na2SO4), and concentrated to dryness. Trituration with Et2O afforded 175 mg (79%) of the desired product. 1H-NMR (DMSO-d6) δ 7.69 (s, 1H), 7.39 (s, 1H), 6.61 (s, 1H), 2.18 (s, 3H); MS [M+H]+=148.9; LCMS RT=1.16.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829185B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-784f3fdca21a43168e8721118d5b2880
출처 메모uspto-grants-2014_09