Реакция #560841

ord-c3626ddc923647bab10de00cd13c2f77

Уравнение реакции

CN(C1CCCCC1)C1CCCCC1
N-cyclohexyl-N-methylcyclohexanamine
C1=COCCC1
3,4-dihydro-2H-pyran
Brc1cccnc1Oc1ccc(Nc2ccccn2)cc1.Cl
N-(4-(3-bromopyridin-2-yloxy)phenyl)pyridin-2-amine hydrochloride
C1=COC(c2cccnc2Oc2ccc(Nc3ccccn3)cc2)CC1
title compound
C1=COC(c2cccnc2Oc2ccc(Nc3ccccn3)cc2)CC1
(±)-N-(4-(3-(3,4-DIHYDRO-2H-PYRAN-2-YL)PYRIDIN-2-YLOXY)PHENYL)PYRIDIN-2-AMINE

Растворители

Условия реакции

Температура
105°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеbefore evacuating
  2. 2
    workup.ADDITIONwas added
  3. 3
    Другоеconsumption of the starting material
  4. 4
    Температураthe reaction mixture was cooled to room temperature
  5. 5
    Другоеthe volatiles were removed under reduced pressure

Методика

To a 25 mL microwave vial was added Bis(tri-tert-butylphosphine) palladium (0) (101 mg, 0.198 mmol) and N-(4-(3-bromopyridin-2-yloxy)phenyl)pyridin-2-amine hydrochloride (750 mg, 1.981 mmol) before evacuating and backfilling with nitrogen (2×). After addition of Dioxane (5.659 ml), N-cyclohexyl-N-methylcyclohexanamine (0.840 ml, 3.96 mmol), and 3,4-dihydro-2H-pyran (666 mg, 7.92 mmol) was added and the mixture was heated to 105° C. Following complete consumption of the starting material, the reaction mixture was cooled to room temperature and the volatiles were removed under reduced pressure. Following silica gel chromatography, the title compound was obtained as a racemic mixture. MS (ESI, pos. ion) m/z: 346.0. IC50 (uM) 0.064.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08637500B2uspto-grants-2014_01