Reaction #502102

ord-29aa95229bf94c9ab0f6c9fa65e31c43

Reaction equation

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

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08088765B2uspto-grants-2012_01