Реакция #68562

ord-48e4ac7d27ae422c99ad679a6ab05836

Растворители

Условия реакции

Температура
100°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas sparged with argon for 5 min
  2. 2
    ДругоеReaction
  3. 3
    Температураcooled
  4. 4
    Другоеthen partitioned between 9:1 CHCl3/IPA (20 mL) and 1M NaOH (15 mL)
  5. 5
    ЭкстракцияAqueous further extracted with 9:1 CHCl3/IPA (2×10 mL)
  6. 6
    СушкаThe combined organics dried over MgSO4
  7. 7
    Концентрированиеconcentrated
  8. 8
    Другоеpurified on 40 g silica eluting with an isocratic 7% 2M NH3 in MeOH/DCM
  9. 9
    ПромывкаProduct further purified prep HPLC eluting with water/ACN (0.1% TFA)
  10. 10
    ДругоеAfter collected fractions
  11. 11
    workup.DISSOLUTIONwas dissolved in 1:1 ACN/water
  12. 12
    ДругоеResulting solid
  13. 13
    Другоеcollected by filteration and solid
  14. 14
    Промывкаwashed with water (2 mL)

Методика

A suspension of 1-(2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanol (228 mg, 807 μmol), N-((6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-methoxy-1,5-naphthyridin-4-amine (197 mg, 576 μmol), dichloro[1,1′bis(diphenylphoshino)ferrocene]palladium(ii)dichloromethane adduct (127 mg, 173 μmol), cesium carbonate (751 mg, 2306 μmol) in dioxane (3 mL) and water (0.6 mL) was sparged with argon for 5 min then heated to 100° C. for 6 h. Reaction cooled then partitioned between 9:1 CHCl3/IPA (20 mL) and 1M NaOH (15 mL). Aqueous further extracted with 9:1 CHCl3/IPA (2×10 mL). The combined organics dried over MgSO4. concentrated, then purified on 40 g silica eluting with an isocratic 7% 2M NH3 in MeOH/DCM. Product further purified prep HPLC eluting with water/ACN (0.1% TFA). After collected fractions were reduced to a clear the residue was dissolved in 1:1 ACN/water and pH adjusted to 9 with 1M NaOH (3-4 drops). Resulting solid collected by filteration and solid washed with water (2 mL). MS (ESI pos. ion) m/z: 462 (MH+). Calc'd exact mass for C23H20ClN7O2: 461.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524900B2uspto-grants-2013_09