Реакция #1244261

ord-a2a76541b7984a3ab2d4e208c38d06c3

Уравнение реакции

O=[N+]([O-])c1ncc[nH]1
2-nitroimidazole
C#CCBr
propargyl bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CN(C)C=O
DMF
C#CCn1ccnc1[N+](=O)[O-]
10
Выход 85.5%
C#CCn1ccnc1[N+](=O)[O-]
2-Nitro-1-(prop-2-ynyl)-1H-imidazole
Выход 85.5%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеreaction
  2. 2
    workup.ADDITIONThe reaction was poured onto water (20 mL)
  3. 3
    Экстракцияextracted into EtOAc (3×20 mL)
  4. 4
    ПромывкаThe combined organics were washed with water (5×20 mL)
  5. 5
    КонцентрированиеThe organic layer was then concentrated in vacuo
  6. 6
    Другоеpurified on a silica gel cartridge

Методика

To a round bottom flask was added 2-nitroimidazole (500 mg, 4.42 mmol), propargyl bromide (631 mg, 5.31 mmol), potassium carbonate (733 mg, 5.31 mmol) and DMF (5 mL). The reaction was stirred overnight at RT. TLC (EtOAc) indicated complete reaction. The reaction was poured onto water (20 mL) and extracted into EtOAc (3×20 mL). The combined organics were washed with water (5×20 mL). The organic layer was then concentrated in vacuo and purified on a silica gel cartridge using EtOAc:Hex as the eluent to afford 571 mg (85% yield) of 10 as a pale yellow solid. 1H NMR (CDCl3, 400 MHz), δ: 2.63 (1H, d, J=5.6 Hz), 5.23 (2H, d, J=2.4 Hz), 7.20 (1H, d, J=1.2 Hz), 7.46 (1H, s). Mass Spec (lo-res): Calc'd for C6H5N3O2: 151.04; found: 152.10 (M+H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07807394B2uspto-grants-2010_10