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HRID 1094897Erstellt: 25. Oktober 2026
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/1094897
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine | HCID 57955201 | — |
| Edukt | HCID 178477796 | HCID 178477796 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 55288621 | 79,8% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08133995B2 |
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| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-8917d9b986fb470e8d6cdd572f5cbb8a |
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| Quellennotiz | uspto-grants-2012_03 |
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