Reacción #502102

ord-29aa95229bf94c9ab0f6c9fa65e31c43

Ecuación de reacción

OCc1cc(-c2ccc3nc(-c4cnc5ccccc5c4)cn3c2)cs1
[4-[(2-quinolin-3-yl)imidazo[1,2-a]pyridin-6-yl]thien-2-yl]methanol
Cl
hydrochloric acid
Cl.OCc1cc(-c2ccc3nc(-c4cnc5ccccc5c4)cn3c2)cs1
compound
Cl.OCc1cc(-c2ccc3nc(-c4cnc5ccccc5c4)cn3c2)cs1
[4-[(2-Quinolin-3-yl)imidazo[1,2-a]pyridin-6-yl]thien-2-yl]methanol hydrochloride

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONare added to the filtrate
  2. 2
    ConcentraciónThe reaction mixture is then concentrated under reduced pressure
  3. 3
    FiltraciónThe precipitate is recovered by filtration
  4. 4
    Otrooven-dried under reduced pressure

Procedimiento

100 mg of [4-[(2-quinolin-3-yl)imidazo[1,2-a]pyridin-6-yl]thien-2-yl]methanol are suspended in dichloromethane and methanol. The solution is passed through a frit and 5.6 ml of a 0.1N solution of hydrochloric acid in isopropanol are added to the filtrate. The reaction mixture is then concentrated under reduced pressure and the residue is then taken up in diethyl ether. The precipitate is recovered by filtration and oven-dried under reduced pressure. 106 mg of compound are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088765B2uspto-grants-2012_01