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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine | HCID 57955201 | — |
| 반응물 | HCID 178477796 | HCID 178477796 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 55288621 | 79.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08829185B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-784f3fdca21a43168e8721118d5b2880 |
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| 출처 메모 | uspto-grants-2014_09 |
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