반응 #73032

ord-ee4d7896f3c94d31bfbdef497c42ae6c

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was heated
  2. 2
    온도at reflux overnight
  3. 3
    농축concentrated under reduced pressure
  4. 4
    기타The residue was triturated with acetonitrile
  5. 5
    기타the resulting solid was isolated by filtration

실험 절차

Trimethylorthobutyrate (1.9 mL, 12.0 mmol) and pyridine hydrochloride (23 mg, 0.2 mmol) were added to a suspension of 4-[(3-amino[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-ol (10.0 mmol) in toluene (50 mL). The reaction mixture was heated at reflux overnight and then concentrated under reduced pressure. The residue was triturated with acetonitrile and the resulting solid was isolated by filtration to provide 2.26 g of 4-[(2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]tetrahydro-2H-pyran-4-ol as a tan solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541438B2uspto-grants-2013_09