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HRID 1094897作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 57955201—
反応物HCID 178477796HCID 178477796—
溶媒1,4-DioxaneHCID 31275—
生成物6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 5528862179.8%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08133995B2
出典データセットuspto-grants-2012_03
ORD IDord-8917d9b986fb470e8d6cdd572f5cbb8a
出典メモuspto-grants-2012_03