반응 #502102

ord-29aa95229bf94c9ab0f6c9fa65e31c43

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08088765B2uspto-grants-2012_01