反応 #502102

ord-29aa95229bf94c9ab0f6c9fa65e31c43

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONare added to the filtrate
  2. 2
    濃縮The reaction mixture is then concentrated under reduced pressure
  3. 3
    ろ過The precipitate is recovered by filtration
  4. 4
    その他oven-dried under reduced pressure

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08088765B2uspto-grants-2012_01