Реакция #487500

ord-762bd504a5d649efb367b630688e8be4

Уравнение реакции

[CH3][Mg][Br]
methyl magnesium bromide
c1ccc(P(CCP(c2ccccc2)c2ccccc2)c2ccccc2)cc1
1,2-bis(diphenylphosphino)ethane
[N-]=[N+]=Nc1ccccc1
phenylazide
C1CCOC1
THF
CC(=O)Nc1ccccc1
Acetoanilide

Условия реакции

Температура
120°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas pre-charged with [11C]CO
  2. 2
    Другоеwas flushed with N2 (the [11C]CO-
  3. 3
    workup.DISSOLUTIONThe solution was dissolved in ammonium formate (0.5 mL, pH=3.5)
  4. 4
    Температураheated at 120° C. for 1 min
  5. 5
    ДругоеA small amount of crude product was collected

Методика

In a capped vial (1 mL) containing a solution of phenylazide (6.6 mg, 55 μmol) in dry THF (300 μL), was added [RhCl(cod)]2 (0.27 mg, 0.55 μmol), and 1,2-bis(diphenylphosphino)ethane (0.66 mg, 1.65 μmol), and was shaken until the solution was homogeneous. After addition of a solution of methyl magnesium bromide (18.5 μL of 3M solution in ether, 55 μmol), the resulting mixture was transferred to the micro-autoclave, which was pre-charged with [11C]CO. The micro-autoclave was heated at 120° C. for 5 min under 35 MPa and the crude product was transferred to a reduced pressure vial. The radioactivity was measured before and after the vial was flushed with N2 (the [11C]CO-trapping efficiency of 96% was determined based on these values). The solution was dissolved in ammonium formate (0.5 mL, pH=3.5) and heated at 120° C. for 1 min. A small amount of crude product was collected and analyzed by the reversed phase HPLC. Yield of product: 91%. The product was identified by HPLC with an added authentic reference compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08741261B2uspto-grants-2014_06