반응 #1869164

ord-1a09d052e34b42498da108bf302c1b78

반응 방정식

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
수율 80.0%

용매

반응 조건

온도
20°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도refluxed under Dean Stark conditions overnight
  2. 2
    workup.DISTILLATIONThe equipment was set for distillation and heptane (18 L)
  3. 3
    기타was removed by distillation
  4. 4
    workup.ADDITIONSeed crystals were added
  5. 5
    기타at 5° C.
  6. 6
    기타overnight
  7. 7
    여과The product was collected by filtration
  8. 8
    세척washed with heptane (2×6 L)
  9. 9
    기타dried at 45° C. under vacuum overnight

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07498329B2uspto-grants-2009_03