反応 #156328

ord-90a5a3ec9c8743f2b363a98f2d86c93a

反応方程式

Cl.Nc1cc(F)c(Br)cn1
5-Bromo-4-fluoro-pyridin-2-ylamine mono HCl salt
C=[CH][Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC
tributyl(vinyl)stannane
C=[CH][Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC
tributyl(vinyl)stannane
C=Cc1cnc(N)cc1F
title product
C=Cc1cnc(N)cc1F
4-Fluoro-5-vinyl-pyridin-2-ylamine

反応条件

温度
120°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed with brine
  2. 2
    乾燥dried over Na2SO4
  3. 3
    ろ過filtered
  4. 4
    その他evaporated to dryness
  5. 5
    その他The residue was purified by chromatography with hexane and EtOAc

実験手順

5-Bromo-4-fluoro-pyridin-2-ylamine mono HCl salt (xvii) (368 mg, 1.62 mmol), tributyl(vinyl)stannane (0.52 mL, 1.78 mmol) and palladium tetrakis(triphenylphosphine) (19 mg, 0.016 mmol) in dioxane (6 mL) under argon were heated under microwave irradiation at 120° C. for 45 min. Were then added tributyl(vinyl)stannane (0.2 mL, 0.685 mmol) and palladium tetrakis(triphenylphosphine) (7 mg, 0.006 mmol) and the RM was placed under argon and heated once more under microwave irradiation at 120° C. for 45 min. The RM was diluted with EtOAc and washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by chromatography with hexane and EtOAc to yield the title product as a yellow solid (tR 1.76 min (conditions 8), MH+=139).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08822468B2uspto-grants-2014_09