Réaction #91124
ord-3f8acd4b546548d781b3c1bae1751008
Équation de réaction
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autreat 0° C
- 2AutreAfter the termination of the reaction
- 3Concentrationthe 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.