反応 #9523

ord-d3476380362741e8b181f688fb0be9e4

溶媒

反応条件

温度
110°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The DMF was removed under reduced pressure
  2. 2
    その他the residue was partitioned between saturated aqueous sodium bicarbonate (40 mL) and dichloromethane (50 mL)
  3. 3
    workup.ADDITIONThe mixture was adjusted to pH 7 with the addition of 10% hydrochloric acid
  4. 4
    workup.DISSOLUTIONwas dissolved with methanol
  5. 5
    濃縮The resulting solution was concentrated under reduced pressure
  6. 6
    その他to provide a solid
  7. 7
    濃縮The aqueous layer was concentrated under reduced pressure
  8. 8
    その他the resulting solid was triturated with methanol
  9. 9
    その他isolated by filtration
  10. 10
    濃縮The filtrate was concentrated under reduced pressure
  11. 11
    その他the residue was triturated
  12. 12
    その他isolated
  13. 13
    その他dried under high vacuum

実験手順

Thiourea (0.29 g, 3.8 mmol) and potassium iodide (0.052 g, 3.1 mmol) were sequentially added to a suspension of 7-bromo-1-(5-chloropentyl)-2-ethoxymethyl-1H-imidazo[4,5-c]quinoline (1.3 g, 3.2 mmol) in DMF (15 mL), and the reaction was heated at 110° C. for 24 hours. The DMF was removed under reduced pressure, and the residue was partitioned between saturated aqueous sodium bicarbonate (40 mL) and dichloromethane (50 mL). The mixture was adjusted to pH 7 with the addition of 10% hydrochloric acid. Product remained on the walls of the reaction flask and was dissolved with methanol. The resulting solution was concentrated under reduced pressure to provide a solid. The aqueous layer was concentrated under reduced pressure, and the resulting solid was triturated with methanol and isolated by filtration. The filtrate was concentrated under reduced pressure, and the residue was triturated and isolated as described above. The isolated solids were combined and dried under high vacuum to provide 1.49 g of 2-[5-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)pentyl]isothiourea hydrochloride as a yellow solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07091214B2uspto-grants-2006_08