Реакция #8358

ord-5117de9338de4a369384dbd7fc1bb107

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеconcentrated in vacuo
  2. 2
    ДругоеThe residue is partitioned between chloroform and saturated sodium chloride
  3. 3
    СушкаThe organic layer is dried (sodium sulfate)
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated in vacuo
  6. 6
    Другоеthe residue chromatographed on SiO2 (dichloromethane to 20% methanol in dichloromethane)

Методика

A solution of 1 M sulfuryl chloride in dichloromethane (20 mL, 20 mmol) is added to a solution of 7-bromo-4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline (2.2 g, 5.62 mmol) in dry pyridine (50 mL). The mixture is stirred for 18 h and concentrated in vacuo. The residue is partitioned between chloroform and saturated sodium chloride. The organic layer is dried (sodium sulfate), filtered, concentrated in vacuo, and the residue chromatographed on SiO2 (dichloromethane to 20% methanol in dichloromethane) to yield the title compound as a red solid, 1.8 g (75%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07087626B2uspto-grants-2006_08