Acetyl chloride → Imiquimod hydrochloride

HRID 1920274ノート

反応式

HRID 1920274 の反応式
C([Cl:4])(=O)C.[NH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[C:12]1[N:16]([CH2:17][CH:18]([CH3:20])[CH3:19])[CH:15]=[N:14][C:13]=1[C:21]#[N:22]>C(O)C>[ClH:4].[CH3:20][CH:18]([CH3:19])[CH2:17][N:16]1[C:12]2[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=3[N:5]=[C:21]([NH2:22])[C:13]=2[N:14]=[CH:15]1

参加物

4

反応物 2

HCID 6367Acetyl chlorideHCID 251645955-(2-aminophenyl)-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile

生成物 1

HCID 13982876Imiquimod hydrochloride収率 23.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

A solution of acetyl chloride (0.15 mL, 2 mmol) in ethanol (2 mL) was added to a solution of 5-(2-aminophenyl)-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile (0.13 g) in ethanol (5 mL). The mixture was heated at reflux for two hours and allowed to cool to ambient temperature. The volume of the mixture was decreased to 2 mL by concentrating under reduced pressure. A solid was present, and the remaining liquid was decanted away from the solid, which was washed with diethyl ether (2×2 mL) and dried overnight in a vacuum oven at room temperature to provide 0.035 g (23% for Example 19 and Example 20 combined) of 1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine hydrochloride as a beige solid, mp>265° C.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for two hours
  3. concentrationby concentrating under reduced pressure
  4. customthe remaining liquid was decanted away from the solid, which
  5. washwas washed with diethyl ether (2×2 mL)
  6. customdried overnight in a vacuum oven at room temperature

出典と根拠

ORDレコード
ord-087d5ed3a94740e9abb0728479f19740
出典データセット
uspto-grants-2012_05
特許番号
US08168802B2

反応ノート

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