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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094897Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 57955201—
ReactantHCID 178477796HCID 178477796—
Solvent1,4-DioxaneHCID 31275—
Product6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 5528862179.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133995B2
Source datasetuspto-grants-2012_03
ORD IDord-8917d9b986fb470e8d6cdd572f5cbb8a
Source noteuspto-grants-2012_03