반응 #44268

ord-c0952ee84e994226b7dcb2797003c9a7

반응 방정식

Brc1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline
Cc1c[nH]cn1
4-methyl-1H-imidazole
[Cs+].[F-]
CsF
Cc1cn(-c2cnc3nnn(Cc4ccc5ncccc5c4)c3n2)cn1
6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline
수율 56.0%

반응 조건

온도
160°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과the resulting suspension was filtered
  2. 2
    세척The precipitate was washed with water
  3. 3
    기타purified by column chromatography
  4. 4
    세척elution with methanol and dichloromethane

실험 절차

A mixture of 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (50 mg, 0.15 mmol), 4-methyl-1H-imidazole (36 mg, 0.44 mmol) and CsF (25 mg, 0.16 mmol) in acetonitrile (1.45 mL) was heated in a microwave to 160° C. for 20 minutes. The reaction was diluted with water (5 mL) and the resulting suspension was filtered. The precipitate was washed with water and then purified by column chromatography using gradient elution with methanol and dichloromethane to afford 6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (28 mg, yield 56%)

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732604B2uspto-grants-2010_06