Реакция #68609

ord-28352e1f17c84e3ea4d08500c9d5cdf7

Уравнение реакции

NN.O
hydrazine hydrate
O=C(c1ccc2ncccc2c1)c1cnc2ccc(-c3ccccc3)nn12
(6-phenylimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanone
[K+].[OH-]
KOH
OCCOCCO
diethylene glycol
c1ccc(-c2ccc3ncc(Cc4ccc5ncccc5c4)n3n2)cc1
6-((6-Phenylimidazo[1,2-b]pyridazin-3-yl)methyl)quinoline

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеsealed
  2. 2
    Экстракцияextracted with DCM (2×75 mL)
  3. 3
    ПромывкаThe combined organics were washed with brine (75 mL)
  4. 4
    Сушкаdried with MgSO4
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated
  7. 7
    Другоеto give a brown solid
  8. 8
    Другоеpurified by prep HPLC
  9. 9
    Другоеto give the product as the formic acid salt

Методика

A 10-20 mL microwave vial was charged with hydrazine hydrate (0.0312 ml, 0.642 mmol), (6-phenylimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanone (0.150 g, 0.428 mmol), KOH (0.0961 g, 1.71 mmol), and diethylene glycol (4.09 ml, 42.8 mmol), sealed, then placed in a Personal Chemistry microwave at 130° C. for 20 minutes after a 5 minute pre-stir. The mixture was diluted with water (75 mL), then extracted with DCM (2×75 mL). The combined organics were washed with brine (75 mL), then dried with MgSO4, filtered, and concentrated to give a brown solid, then purified by prep HPLC to give the product as the formic acid salt. MS (ESI pos. ion) m/z: 337 (MH+). Calc'd exact mass for C22H16N4: 336.

Источник

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