Реакция #502102

ord-29aa95229bf94c9ab0f6c9fa65e31c43

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08088765B2uspto-grants-2012_01