反応 #1869164

ord-1a09d052e34b42498da108bf302c1b78

反応方程式

Nc1ccc(Br)cn1
2-Amino-5-bromopyridine
CC(=O)CCC(C)=O
2,5-hexanedione
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
Cc1ccc(C)n1-c1ccc(Br)cn1
5-Bromo-2-(2,5-dimethylpyrrol-1-yl)pyridine
収率 80.0%

溶媒

反応条件

温度
20°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度refluxed under Dean Stark conditions overnight
  2. 2
    workup.DISTILLATIONThe equipment was set for distillation and heptane (18 L)
  3. 3
    その他was removed by distillation
  4. 4
    workup.ADDITIONSeed crystals were added
  5. 5
    その他at 5° C.
  6. 6
    その他overnight
  7. 7
    ろ過The product was collected by filtration
  8. 8
    洗浄washed with heptane (2×6 L)
  9. 9
    その他dried at 45° C. under vacuum overnight

実験手順

2-Amino-5-bromopyridine (6.0 Kg, 34.7 mol), 2,5-hexanedione (4.35 Kg, 38.2 mol) and p-toluenesulfonic acid (12 g) were dissolved in heptane (36 L) and refluxed under Dean Stark conditions overnight. The equipment was set for distillation and heptane (18 L) was removed by distillation. The mixture was cooled to 20° C. for 60 minutes. Seed crystals were added and the mixture granulated at 20° C. for 2 hours and then at 5° C. overnight. The product was collected by filtration, washed with heptane (2×6 L) and dried at 45° C. under vacuum overnight. Yield=80% (7.0 Kg) δH (CDCl3 300 MHz) 2.20 (6H, s), 5.95 (2H, s), 7.15 (1H, d), 7.95 (1H, d), 8.70 (1H, s) ppm. MS m/z 253 (MH+, Br isotope).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07498329B2uspto-grants-2009_03