6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine → 6-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amine

HRID 73703

反応式

HRID 73703 の反応式
Br[C:2]1[CH:3]=[C:4]2[N:9]([CH:10]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH2:11].[CH3:12][Zn]C>O1CCOCC1>[CH3:12][C:2]1[CH:3]=[C:4]2[N:9]([CH:10]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH2:11]

参加物

4

反応条件

温度
90 °C

実験手順

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.

後処理

  1. temperaturecooled to 0° C
  2. customThe reaction was quenched with MeOH (1.0 mL)
  3. custompartitioned between ethyl acetate (200 mL) and potassium phosphate dibasic pH 10 buffer (100 mL)
  4. customThe layers were separated
  5. washthe organic phase was washed with brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-784f3fdca21a43168e8721118d5b2880
出典データセット
uspto-grants-2014_09
特許番号
US08829185B2

関連ノート

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