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HRID 73703Erstellt: 26. 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/73703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 57955201—
EduktHCID 178477796HCID 178477796—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 5528862179,8%

Reaktionsbedingungen

Temperatur90 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829185B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-784f3fdca21a43168e8721118d5b2880
Quellennotizuspto-grants-2014_09