2,5-Dimethoxytetrahydrofuran → 1-(2-methylpropyl)-8-(1-pyrrolyl)-1H-imidazo[4,5-c]quinolin-4-amine

HRID 9473

反応式

HRID 9473 の反応式
CO[CH:3]1[CH2:7][CH2:6][CH:5](OC)O1.[NH2:10][C:11]1[CH:20]=[CH:19][C:18]2[N:17]=[C:16]([NH2:21])[C:15]3[N:22]=[CH:23][N:24]([CH2:25][CH:26]([CH3:28])[CH3:27])[C:14]=3[C:13]=2[CH:12]=1>C(O)(=O)C>[CH3:27][CH:26]([CH3:28])[CH2:25][N:24]1[C:14]2[C:13]3[CH:12]=[C:11]([N:10]4[CH:3]=[CH:7][CH:6]=[CH:5]4)[CH:20]=[CH:19][C:18]=3[N:17]=[C:16]([NH2:21])[C:15]=2[N:22]=[CH:23]1

参加物

4

実験手順

2,5-Dimethoxytetrahydrofuran (1.6 mL of 95%, 12 mmol) was added to a suspension of 8-amino-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine (3.0 g, 12 mmol) in acetic acid (60 mL), and the reaction was heated at reflux for one hour. The resulting dark brown solution was concentrated under reduced pressure, and the residue was mixed with water. The resulting mixture was made basic with the addition of ammonium hydroxide and stirred for 30 minutes. The resulting precipitate was isolated by filtration, washed with water, dried, and recrystallized from ethanol (100 mL). The crystals were collected in three crops. The first crop was dried for a day in a vacuum oven at 100° C. to provide 2.1 g of 1-(2-methylpropyl)-8-(1-pyrrolyl)-1H-imidazo[4,5-c]quinolin-4-amine as a solid, mp 227.5–231.5° C.

後処理

  1. temperaturethe reaction was heated
  2. temperatureat reflux for one hour
  3. concentrationThe resulting dark brown solution was concentrated under reduced pressure
  4. additionthe residue was mixed with water
  5. additionThe resulting mixture was made basic with the addition of ammonium hydroxide
  6. customThe resulting precipitate was isolated by filtration
  7. washwashed with water
  8. customdried
  9. customrecrystallized from ethanol (100 mL)
  10. customThe crystals were collected in three crops
  11. customThe first crop was dried for a day in a vacuum oven at 100° C.

出典と根拠

ORDレコード
ord-bdb211b4df684f309f1596fd2503ee77
出典データセット
uspto-grants-2006_08
特許番号
US07091214B2

関連ノート

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