Réaction #91124

ord-3f8acd4b546548d781b3c1bae1751008

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat 0° C
  2. 2
    AutreAfter the termination of the reaction
  3. 3
    Concentrationthe reactant was concentrated under reduced pressure

Mode opératoire

(2-Cyclopentylsulfanyl-pyridin-3-yl)-methanol (0.6 g, 2.87 mmol) obtained in Step B was dissolved in CH3CN (5 mL), and SOCl2(0.42 mL, 5.74 mmol) was added thereto at 0° C. The mixture was stirred at room temperature for 2 hours. After the termination of the reaction, the reactant was concentrated under reduced pressure to obtain the title compound, which was used in the next step without a separate purification process.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09447044B2uspto-grants-2016_09