1,1'-Carbonyldiimidazole → HCID 22936848, compound

HRID 387729Notes

Reaction equation

HRID 387729 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:21]=[CH:20][C:19]([NH:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[NH2:30])=[CH:18][CH:17]=1.[C:31](N1C=CN=C1)(N1C=CN=C1)=[O:32]>CN(C)C=O.O1CCCC1.O>[NH:30]1[C:25]2[C:24](=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH2:23][N:22]([C:19]2[CH:18]=[CH:17][C:16]([O:15][C:6]3[C:5]4[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=4)[N:9]=[CH:8][CH:7]=3)=[CH:21][CH:20]=2)[C:31]1=[O:32]

Participants

6

Conditions

Temperature
70 °C

Procedure

6,7-Dimethoxy-4-(4-(2-aminophenyl)methylaminophenyloxy)quinoline (40 mg, 0.0996 mmol) was dissolved in dimethylformamide (0.5 ml), 1,1′-carbonyldiimidazole (19 mg, 0.1196 mmol) was added, and the mixture was stirred at 70° C. for 8 hours. After cooling to room temperature, the reaction solution was diluted with tetrahydrofuran, water was added, and the mixture was extracted with ethyl acetate, washed with saturated saline and dried over anhydrous magnesium sulfate, after which the solvent was distilled off under reduced pressure. The residue was purified with a silica gel column (ethyl acetate-methanol system) and recrystallized with hexane-diethyl ether to obtain the title compound (3 mg, 0.0070 mmol, 7.05%) as colorless crystals.

Workup

  1. temperatureAfter cooling to room temperature
  2. additionwas added
  3. extractionthe mixture was extracted with ethyl acetate
  4. washwashed with saturated saline
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationafter which the solvent was distilled off under reduced pressure
  7. customThe residue was purified with a silica gel column (ethyl acetate-methanol system)
  8. customrecrystallized with hexane-diethyl ether

Sources & evidence

ORD record
ord-fb7d17ff091a43c58f4116e6f65c57a3
Source dataset
uspto-grants-2013_02
Patent number
US08372981B2

Reaction notes

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