Реакция #88043

ord-940df2b609564ca49e67ea9a7eb5af63

Уравнение реакции

O=C([O-])[O-].[Na+].[Na+]
Na2CO3
COc1ccnc(N)c1I
3-iodo-4-methoxypyridin-2-amine
F[B-](F)(F)F.[H+]
HBF4
O=N[O-].[Na+]
NaNO2
COc1ccnc(F)c1I
2-fluoro-3-iodo-4-methoxypyridine

Реагенты

Нет

Растворители

Условия реакции

Температура
-20°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGThe mixture was stirred at 0° C. for 3 h
  2. 2
    ЭкстракцияThe layer was then extracted with EtOAc (×3)
  3. 3
    СушкаThe combined organic layers were dried over anhydrous MgSO4
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated under vacuum
  6. 6
    Другоеto leave a residue which
  7. 7
    Другоеwas purified by column chromatography on silica gel (elution with 5:1 to 2:1 hexanes:ethyl acetate)

Методика

To a cold (−20° C.), stirred suspension of the 3-iodo-4-methoxypyridin-2-amine (2.5 g, 10 mmol) in HBF4 (70 mL, 470 mmol) was added an aqueous solution of NaNO2 (1.67 M, 6 mL, 10 mmol) over 20 min. The reaction turned green and then brown in color. The mixture was stirred at 0° C. for 3 h. The reaction was then carefully poured into a cold (0° C.) saturated solution of Na2CO3 (50 g) in H2O (100 mL). The layer was then extracted with EtOAc (×3). The combined organic layers were dried over anhydrous MgSO4, filtered, and concentrated under vacuum to leave a residue which was purified by column chromatography on silica gel (elution with 5:1 to 2:1 hexanes:ethyl acetate) to yield 2-fluoro-3-iodo-4-methoxypyridine as a light yellow solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09440952B2uspto-grants-2016_09